Difference between revisions of "FlyBase:Papers with technical advances"

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= Popular Resource Categories =
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|style="text-align: center; padding: 15px;"| <big>[[FlyBase:External_Resources|All Resources]]</big> ||style="text-align: center; padding: 20px;"| <big>[[FlyBase:CRISPR|CRISPR]]</big> ||style="text-align: center; padding: 20px;"| <big>[[FlyBase:ScRNA-Seq|ScRNA-Seq]]</big> ||style="text-align: center; padding: 20px;"| <big>[[FlyBase:RNAi|RNAi]]</big> ||style="text-align: center; padding: 20px;"| <big>[[FlyBase:Stocks|Stocks]]</big> ||style="text-align: center; padding: 20px;"| <big>[[FlyBase: Antibodies|Antibodies]]</big>||style="text-align: center; padding: 20px;"| <big>[[FlyBase:Neuroscience|Neuroscience]]</big>
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|style="text-align: center; padding: 20px;"| <big>[[FlyBase:Model_Organism_Databases|Model Organism<br/> Databases]]</big> ||style="text-align: center; padding: 20px;"| <big>[[FlyBase:Images|Images]]</big> ||style="text-align: center; padding: 20px;"| <big>[[FlyBase:Maps|Maps]]</big> ||style="text-align: center; padding: 20px;"| <big>[http://www.flyrnai.org/tools/protocols/web/ Protocols]</big> ||style="text-align: center; padding: 20px;"| <big>[[FlyBase:Papers_with_technical_advances|Papers with<br/> Technical Advances]]</big>
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__TOC__
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==Overview==
 
==Overview==
Authors of the papers listed below suggest that they include a technical advance, new type of reagent, or resource likely to be useful for other researchers. Author suggestions have been collected via the Fast-Track Your Paper tool since October 2020, with those most recently submitted at the top. Please note, there will be a lag time before listed papers can be found on FlyBase and the submission date does not necessarily match the publication date of the paper.
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Authors of the papers listed below suggest that they include a technical advance, new type of reagent, or resource likely to be useful for other researchers. Author suggestions have been collected via the Fast-Track Your Paper tool since October 2020, with those most recently submitted at the top. Please note, there will be a lag time before listed papers can be found on FlyBase (FBrf links will become active when available) and the submission date does not necessarily match the publication date of the paper.
  
 
==Technical Advances==
 
==Technical Advances==
 
 
 
===2021===
 
===2021===
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==== May 2021====
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{| class="wikitable"
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|-
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! ''Author description of technical advance''!!''Title''!!''Journal''!!''PubMed ID''!! ''FBrf number''
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|-
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| Quantitative analysis of parkin-dependent mitophagy using confocal microscopy||3D quantification of autophagy activation and autophagosome-to-mitochondria recruitment in a Drosophila model of Parkinson's disease.||STAR Protoc||[https://pubmed.ncbi.nlm.nih.gov/33851139 33851139]||[https://flybase.org/reports/FBrf0248763 FBrf0248763]
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|- bgcolor="lightgrey"
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| Seahorse experiments on cardiac tissue||Fat-body brummer lipase determines survival and cardiac function during starvation in Drosophila melanogaster.||iScience||[https://pubmed.ncbi.nlm.nih.gov/33889813 33889813]||[https://flybase.org/reports/FBrf0248791 FBrf0248791]
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|-
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| Development of proteomics of protein trafficking||Proteomics of protein trafficking by in vivo tissue-specific labeling.||Nat. Commun.||[https://pubmed.ncbi.nlm.nih.gov/33888706 33888706]||[https://flybase.org/reports/FBrf0248752 FBrf0248752]
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|- bgcolor="lightgrey"
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| Antibodies generated for AIF and DNase II||DNase II mediates a parthanatos-like developmental cell death pathway in Drosophila primordial germ cells.||Nat. Commun.||[https://pubmed.ncbi.nlm.nih.gov/33863891 33863891]||[https://flybase.org/reports/FBrf0248742 FBrf0248742]
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|-
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| A novel Drosophila model for mild traumatic brain injury for investigation of lifelong brain deficits and degeneration, it also has a new imaging-based approach for analyzing brain pathology in whole mount brains. ||Repetitive mild head trauma induces activity mediated lifelong brain deficits in a novel Drosophila model.||Sci. Rep.||[https://pubmed.ncbi.nlm.nih.gov/33958652 33958652]||[https://flybase.org/reports/FBrf0248899 FBrf0248899]
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|- bgcolor="lightgrey"
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| We generated a roGFP-CAAX construct (for mammalian expression) that can be used to examine the redox-state on the plasma membrane.||Dihydroceramide desaturase regulates the compartmentalization of Rac1 for neuronal oxidative stress.||Cell Rep.||[https://pubmed.ncbi.nlm.nih.gov/33852856 33852856]||[https://flybase.org/reports/FBrf0248757 FBrf0248757]
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|-
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| A fluorogen activating protein neuropeptide (Dilp2-FAP) construct was used with membrane impermeant malachite green derivatives (MG-TCarb and MG-B-Tau) to detect neuropeptide release in the brain, specifically in LNv clock neurons||Temporally and spatially partitioned neuropeptide release from individual clock neurons.||Proc. Natl. Acad. Sci. U.S.A.||[https://pubmed.ncbi.nlm.nih.gov/33875606 33875606]||[https://flybase.org/reports/FBrf0248728 FBrf0248728]
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|- bgcolor="lightgrey"
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| Here we design a microfluidic device capable of ensuring the normal development of multiple fly embryos as well as achieving real-time temperature control and fast temperature switches for quantitative live imaging with a home-built two-photon microscope. ||Quantifying Temperature Compensation of Bicoid Gradients with a Fast T-Tunable Microfluidic Device.||Biophys. J.||[https://pubmed.ncbi.nlm.nih.gov/32853562 32853562]||[https://flybase.org/reports/FBrf0248966 FBrf0248966]
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|-
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| We use whole-genome sequencing of Drosophila tissues (gut, head) to discover somatic genetic variation: 1- short-read Illumina sequencing of low-input DNA isolated from spontaneous clonal gut neoplasia, 2- long-read Oxford Nanopore (ONT) sequencing of DNA from pooled tissues.||Unraveling the features of somatic transposition in the Drosophila intestine.||EMBO J.||[https://pubmed.ncbi.nlm.nih.gov/33634906 33634906]||[https://flybase.org/reports/FBrf0248816 FBrf0248816]
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|- bgcolor="lightgrey"
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| The work uses the isotropic fractionator method with Drosophila and mosquito brains.  This method allows counting the number of cells in a tissue.  If can be used with an antibody or genetic labeling (GAL4/UAS or QF/QUAS) and be applied to counting sub-populations of a tissue.||The number of neurons in Drosophila and mosquito brains.||PLoS ONE||[https://pubmed.ncbi.nlm.nih.gov/33989293 33989293]||[https://flybase.org/reports/FBrf0248958 FBrf0248958]
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|-
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| GRAF plays a role in restricting the constriction of the actomyosin based contractile ring in cellularization.||Spatiotemporal recruitment of RhoGTPase protein GRAF inhibits actomyosin ring constriction in Drosophila cellularization.||eLife||[https://pubmed.ncbi.nlm.nih.gov/33835025 33835025]||[https://flybase.org/reports/FBrf0248856 FBrf0248856]
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|- bgcolor="lightgrey"
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|}
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==== Apr 2021====
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{| class="wikitable"
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|-
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! ''Author description of technical advance''!!''Title''!!''Journal''!!''PubMed ID''!! ''FBrf number''
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|-
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| We have developed an automated imaging system constituted of a light sheet fluorescence microscope on a chip that allows analysis of Drosophila embryos in suspension that are fluxing in through a microfluidic chamber.||Automatic imaging of Drosophila embryos with light sheet fluorescence microscopy on chip.||J. Biophotonics||[https://pubmed.ncbi.nlm.nih.gov/33295053 33295053]||[https://flybase.org/reports/FBrf0248287 FBrf0248287]
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|- bgcolor="lightgrey"
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| Method to quantify epithelial barrier permeability in Drosophila imaginal discs using fluorescent dextran. The permeability of the experimental sample is compared to control samples that have a disrupted or non-functional barrier. Modified from Lamb et al. (1998).||Ecdysone regulates the Drosophila imaginal disc epithelial barrier, determining the length of regeneration checkpoint delay.||Development||[https://pubmed.ncbi.nlm.nih.gov/33658221 33658221]||[https://flybase.org/reports/FBrf0248455 FBrf0248455]
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| We developed PEGASUS_flies, which calculates whole gene significance scores from variant P-values that were output in a GWAS. Our platform works well for Drosophila/Drosophila Genetic Reference Panel (DGRP) lines.  Available at: https://github.com/ramachandran-lab/PEGASUS_flies||Natural variation in the regulation of neurodevelopmental genes modifies flight performance in Drosophila.||PLoS Genet.||[https://pubmed.ncbi.nlm.nih.gov/33735180 33735180]||[https://flybase.org/reports/FBrf0248437 FBrf0248437]
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|- bgcolor="lightgrey"
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| Hypoxia chamber with strictly controlled environmental parameters||Posthypoxic behavioral impairment and mortality of Drosophila melanogaster are associated with high temperatures, enhanced predeath activity and oxidative stress.||Exp. Mol. Med.||[https://pubmed.ncbi.nlm.nih.gov/33564101 33564101]||[https://flybase.org/reports/FBrf0248297 FBrf0248297]
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|-
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| We introduced DrosoX technique (Scitech Korea, Republic of Korea) for the quantitative analysis of food intake by individual flies.||Cucurbitacin B Suppresses Hyperglycemia Associated with a High Sugar Diet and Promotes Sleep in Drosophila melanogaster.||Mol. Cells||[https://pubmed.ncbi.nlm.nih.gov/33542166 33542166]||[https://flybase.org/reports/FBrf0248331 FBrf0248331]
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|- bgcolor="lightgrey"
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| The "resource" is an accurate phylogeny for the montium group of Drosophila||A phylogeny for the Drosophila montium species group: A model clade for comparative analyses.||Molec. Phylog. Evol.||[https://pubmed.ncbi.nlm.nih.gov/33387647 33387647]||[https://flybase.org/reports/FBrf0248412 FBrf0248412]
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|-
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| UAS-based transgenic lines for expressing genes from the SARS-CoV-2 virus that causes COVID-19 were generated.||Functional analysis of SARS-CoV-2 proteins in Drosophila identifies Orf6-induced pathogenic effects with Selinexor as an effective treatment.||Cell Biosci.||[https://pubmed.ncbi.nlm.nih.gov/33766136 33766136]||[https://flybase.org/reports/FBrf0248509 FBrf0248509]
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|- bgcolor="lightgrey"
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| Targated DamID of olfactory sensory neuron populations||Targeted molecular profiling of rare olfactory sensory neurons identifies fate, wiring, and functional determinants.||eLife||[https://pubmed.ncbi.nlm.nih.gov/33666172 33666172]||[https://flybase.org/reports/FBrf0248540 FBrf0248540]
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|-
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| pPWG-attB empty vector. A modified pPWG vector bearing the attB region inserted at a StuI site. It is compatible with Gateway system and can be used for random insertion in the genome (as a standard pPWG) but also in attB/P site specific integration ( phiC31 mediated).||Mauve/LYST limits fusion of lysosome-related organelles and promotes centrosomal recruitment of microtubule nucleating proteins.||Dev. Cell||[https://pubmed.ncbi.nlm.nih.gov/33725482 33725482]||[https://flybase.org/reports/FBrf0248552 FBrf0248552]
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|- bgcolor="lightgrey"
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| Identification of mRNA targets of Ataxin2 (Atx2) in Drosophila brain by fusing it to the catalytic domain of adenosine deaminase (ADAR) enzyme. ADAR converts adenosine into inosine and subsequent RNA-Seq identifies these conversions (edits) as guanosines.||Antagonistic roles for Ataxin-2 structured and disordered domains in RNP condensation.||eLife||[https://pubmed.ncbi.nlm.nih.gov/33689682 33689682]||[https://flybase.org/reports/FBrf0248408 FBrf0248408]
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|-
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| Single molecule fluorescence in situ hybridisation in whole Drosophila brain.||Selective dendritic localization of mRNA in Drosophila mushroom body output neurons.||eLife||[https://pubmed.ncbi.nlm.nih.gov/33724180 33724180]||[https://flybase.org/reports/FBrf0248505 FBrf0248505]
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|- bgcolor="lightgrey"
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| Novel method to compare 3D chromatin conformation data in Drosophila||Independence of chromatin conformation and gene regulation during Drosophila dorsoventral patterning.||Nat. Genet.||[https://pubmed.ncbi.nlm.nih.gov/33795866 33795866]||[https://flybase.org/reports/FBrf0248615 FBrf0248615]
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|-
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| A lineage recording system termed "intMEMOIR" designed for in situ readout, thereby enabling simultaneous analysis of cell lineage, state, and spatial organization in the same tissue. ||Imaging cell lineage with a synthetic digital recording system.||Science||[https://pubmed.ncbi.nlm.nih.gov/33833095 33833095]||[https://flybase.org/reports/FBrf0248662 FBrf0248662]
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|- bgcolor="lightgrey"
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|}
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==== Mar 2021====
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{| class="wikitable"
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|-
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! ''Author description of technical advance''!!''Title''!!''Journal''!!''PubMed ID''!! ''FBrf number''
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|-
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| We describe a fluorescent in situ hybridization protocol for the detection of endogenous Drosophila gut microbiome bacteria in different sample types (isolated bacteria, feces, larval and adult guts). We also added an automated analysis pipeline, which should be useful for others.||Visualization of endogenous gut bacteria in Drosophila melanogaster using fluorescence in situ hybridization.||PLoS ONE||[https://pubmed.ncbi.nlm.nih.gov/33606846 33606846 ]||[https://flybase.org/reports/FBrf0248171 FBrf0248171]
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|- bgcolor="lightgrey"
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| FreeClimber is an automated and high-throughput method for accurately and repeatably quantifying group climbing performance/climbing velocity/negative geotaxis in Drosophila. For more information, see the GitHub repository at: https://github.com/adamspierer/freeclimber||FreeClimber: automated quantification of climbing performance in Drosophila.||J. Exp. Biol.||[https://pubmed.ncbi.nlm.nih.gov/33188065 33188065 ]||[https://flybase.org/reports/FBrf0247781 FBrf0247781]
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|-
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| CLADES, a tool to analyze neuronal lineages in Drosophila.||A programmable sequence of reporters for lineage analysis.||Nat. Neurosci.||[https://pubmed.ncbi.nlm.nih.gov/32719561 32719561 ]||[https://flybase.org/reports/FBrf0247972 FBrf0247972]
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|- bgcolor="lightgrey"
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| The paper describes the use of Hedgehog signaling compenents: The signal Hedgehog and receptor Patched directed expression to model mutually exclusive computations in the context and highlights useful applications and tries to imagine the technology's potential. ||A Turing machine for the Life Sciences.||D. I. S.||||[https://flybase.org/reports/FBrf0248044 FBrf0248044]
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|-
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| New antibody, new transgenic lines, new S2 cell stable cell lines.||Drosophila Tubulin-Specific Chaperone E Recruits Tubulin around Chromatin to Promote Mitotic Spindle Assembly.||Curr. Biol.||[https://pubmed.ncbi.nlm.nih.gov/33259793 33259793 ]||[https://flybase.org/reports/FBrf0248211 FBrf0248211]
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|- bgcolor="lightgrey"
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| In this manuscript it is reported a new setup to evaluate for the first time the release of neuroactive amines in Drosophila brain, by in vivo Fast-Scan Cyclic Voltammetry, while the fly is being exposed to odorants or an electric shock.||Study of the release of endogenous amines in Drosophila brain in vivo in response to stimuli linked to aversive olfactory conditioning.||J. Neurochem.||[https://pubmed.ncbi.nlm.nih.gov/32596813 32596813 ]||[https://flybase.org/reports/FBrf0248195 FBrf0248195]
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|-
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| Generation of novel transgenic flies expressing a monocistronic version of the human FUS gene (expresses only the FUS protein or only the altFUS protein), as well as the wild-type human FUS gene (expresses both proteins, FUS and altFUS).||The FUS gene is dual-coding with both proteins contributing to FUS-mediated toxicity.||EMBO Rep.||[https://pubmed.ncbi.nlm.nih.gov/33226175 33226175 ]||[https://flybase.org/reports/FBrf0248130 FBrf0248130]
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|- bgcolor="lightgrey"
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| Gene Drive element (split) located in specific Drosophila melanogaster genes.||Inherently confinable split-drive systems in Drosophila.||Nat. Commun.||[https://pubmed.ncbi.nlm.nih.gov/33674604 33674604 ]||[https://flybase.org/reports/FBrf0248266 FBrf0248266]
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|-
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| By using the previously defined matrisomes of Drosophila, we analyzed recorded genotype-to-phenotype relationships to define the Drosophila extracellular matrix phenome.||The extracellular matrix phenome across species.||Matrix Biol Plus||[https://pubmed.ncbi.nlm.nih.gov/33543035 33543035 ]||[https://flybase.org/reports/FBrf0247970 FBrf0247970]
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|- bgcolor="lightgrey"
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| This article indicates the maximum length of introgession segments that produce hybrid segmental offspring in heterozygosity, introgressing chromosomal segments of D. koepferae into a genetic background of D. buzzatii.||Evaluation of Drosophila chromosomal segments proposed by means of simulations of possessing hybrid sterility genes from reproductive isolation.||J. Genet.||[https://pubmed.ncbi.nlm.nih.gov/33622987 33622987 ]||[https://flybase.org/reports/FBrf0248240 FBrf0248240]
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|}
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==== Feb 2021====
 
==== Feb 2021====
 
{| class="wikitable"
 
{| class="wikitable"
 
|-
 
|-
! ''FBrf number''!!''PubMed ID''!!''Journal''!!''Title''!!''Author description of technical advance''
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! ''Author description of technical advance''!!''Title''!!''Journal''!!''PubMed ID''!! ''FBrf number''
 
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| FBrf0247772 || [https://pubmed.ncbi.nlm.nih.gov/33443210/ 33443210] || Proc. Natl. Acad. Sci. U.S.A. || Precise genome engineering in Drosophila using prime editing.|| This paper describes reagents (e.g. transgenic flies, plasmids, cloning protocols) to perform prime editing in Drosophila melanogaster.
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| This paper describes reagents (e.g. transgenic flies, plasmids, cloning protocols) to perform prime editing in Drosophila melanogaster.|| Precise genome engineering in Drosophila using prime editing.|| Proc. Natl. Acad. Sci. U.S.A. ||[https://pubmed.ncbi.nlm.nih.gov/33443210/ 33443210 ]||[https://flybase.org/reports/FBrf0247772 FBrf0247772]
 
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| FBrf0247854 || [https://pubmed.ncbi.nlm.nih.gov/31712250/ 31712250] || J. Lipid Res. || Lipidome-wide 13C flux analysis: a novel tool to estimate the turnover of lipids in organisms and cultures.||Metabolic flux analysis of lipids
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| Metabolic flux analysis of lipids.|| Lipidome-wide 13C flux analysis: a novel tool to estimate the turnover of lipids in organisms and cultures. || J. Lipid Res. ||[https://pubmed.ncbi.nlm.nih.gov/31712250/ 31712250] || [https://flybase.org/reports/FBrf0247854 FBrf0247854]
 
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| FBrf0247762 || [https://pubmed.ncbi.nlm.nih.gov/33149298/ 33149298] || Nature || Neuronal diversity and convergence in a visual system developmental atlas.||Developmental scRNA-seq atlas of the Drosophila optic lobe
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| Developmental scRNA-seq atlas of the Drosophila optic lobe. || Neuronal diversity and convergence in a visual system developmental atlas. || Nature ||[https://pubmed.ncbi.nlm.nih.gov/33149298/ 33149298] || [https://flybase.org/reports/FBrf0247762 FBrf0247762]
 
|- bgcolor="lightgrey"
 
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| FBrf0247932 || [https://pubmed.ncbi.nlm.nih.gov/33025430/ 33025430] || Environ. Sci. Pollut. Res. Int. || Genes regulating development and behavior exhibited altered expression in Drosophila melanogaster exposed to bisphenol A: use of real-time quantitative PCR (qRT-PCR) and droplet digital PCR (ddPCR) in genotoxicity study.||Application of digital droplet PCR in gene expression study
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| Application of digital droplet PCR in gene expression study.|| Genes regulating development and behavior exhibited altered expression in Drosophila melanogaster exposed to bisphenol A: use of real-time quantitative PCR (qRT-PCR) and droplet digital PCR (ddPCR) in genotoxicity study. || Environ. Sci. Pollut. Res. Int.  || [https://pubmed.ncbi.nlm.nih.gov/33025430/ 33025430] || [https://flybase.org/reports/FBrf0247932 FBrf0247932]
 
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| FBrf0247834 || [https://pubmed.ncbi.nlm.nih.gov/33346099/ 33346099] || Gene || Characterization of the Drosophila suzukii β2-tubulin gene and the utilization of its promoter to monitor sex separation and insemination.||The transgenic sexing strains of Drosophila suzukii based on the testis-specific fluorescent expression.  
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| The transgenic sexing strains of Drosophila suzukii based on the testis-specific fluorescent expression.|| Characterization of the Drosophila suzukii β2-tubulin gene and the utilization of its promoter to monitor sex separation and insemination. || Gene ||[https://pubmed.ncbi.nlm.nih.gov/33346099/ 33346099] || [https://flybase.org/reports/FBrf0247834 FBrf0247834]
 
|- bgcolor="lightgrey"
 
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| FBrf0247838 || [https://pubmed.ncbi.nlm.nih.gov/33490883/ 33490883] || FASEB Bioadv || Preference and detrimental effects of high fat, sugar, and salt diet in wild-caught Drosophila simulans are reversed by flight exercise.||New model of Flight exercise. New model of the Western Diet
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| New model of flight exercise, new model of the Western Diet. || Preference and detrimental effects of high fat, sugar, and salt diet in wild-caught Drosophila simulans are reversed by flight exercise.|| FASEB Bioadv ||[https://pubmed.ncbi.nlm.nih.gov/33490883/ 33490883] || [https://flybase.org/reports/FBrf0247838 FBrf0247838]
 
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| FBrf0247869 || [https://pubmed.ncbi.nlm.nih.gov/33495334/ 33495334] || Proc. Natl. Acad. Sci. U.S.A. || Drosophila Sex Peptide controls the assembly of lipid microcarriers in seminal fluid.||Identification of neutral lipid-based secreted structures called microcarriers in the lumen of the male accessory gland, which can be stained by neutral lipid dyes like LipidTox and Nile Red.
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| Identification of neutral lipid-based secreted structures called microcarriers in the lumen of the male accessory gland, which can be stained by neutral lipid dyes like LipidTox and Nile Red.|| Drosophila Sex Peptide controls the assembly of lipid microcarriers in seminal fluid. || Proc. Natl. Acad. Sci. U.S.A. ||[https://pubmed.ncbi.nlm.nih.gov/33495334/ 33495334] || [https://flybase.org/reports/FBrf0247869 FBrf0247869]
 
|- bgcolor="lightgrey"
 
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| FBrf0247944 || [https://pubmed.ncbi.nlm.nih.gov/33514834/ 33514834] || Commun. Biol. || The level of oncogenic Ras determines the malignant transformation of Lkb1 mutant tissue in vivo.||Long-term in vivo imaging of Drosophila giant larvae tumor migration and invasion using SiMView microscopy.
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| Long-term in vivo imaging of Drosophila giant larvae tumor migration and invasion using SiMView microscopy.|| The level of oncogenic Ras determines the malignant transformation of Lkb1 mutant tissue in vivo. || Commun. Biol.|| [https://pubmed.ncbi.nlm.nih.gov/33514834/ 33514834] || [https://flybase.org/reports/FBrf0247944 FBrf0247944]
 
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| FBrf0247996 || [https://pubmed.ncbi.nlm.nih.gov/33532738/ 33532738] || STAR Protoc || Analyzing muscle structure and function throughout the larval instars in live Drosophila.||Methods to examine the musculature of the Drosophila larva. These methods include analysis of the muscle sarcomeres, particularly in the same larva throughout the different larval instars. This work contains methods to muscle structural changes to muscle functional changes.
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| Methods to examine the musculature of the Drosophila larva. These methods include analysis of the muscle sarcomeres, particularly in the same larva throughout the different larval instars. This work contains methods to muscle structural changes to muscle functional changes. || Analyzing muscle structure and function throughout the larval instars in live Drosophila. || STAR Protoc ||[https://pubmed.ncbi.nlm.nih.gov/33532738/ 33532738] || [https://flybase.org/reports/FBrf0247996 FBrf0247996]
 
|- bgcolor="lightgrey"
 
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| FBrf0248021 || [https://pubmed.ncbi.nlm.nih.gov/33537561/ 33537561] || Micropub Biol || Serum-free adapted Drosophila S2R+ line is amenable to RNA interference.||We verified that Drosophila S2R+ adapted to grow in serum-free media is amenable to RNAi interference-mediated gene knockdown.  
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| We verified that Drosophila S2R+ adapted to grow in serum-free media is amenable to RNAi interference-mediated gene knockdown. || Serum-free adapted Drosophila S2R+ line is amenable to RNA interference. || Micropub Biol || [https://pubmed.ncbi.nlm.nih.gov/33537561/ 33537561] || [https://flybase.org/reports/FBrf0248021 FBrf0248021]
 
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| FBrf0248088 || [https://pubmed.ncbi.nlm.nih.gov/33563972/ 33563972] || Nat. Commun. || Dynamic sex chromosome expression in Drosophila male germ cells.||single cell genomics of testes
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| Single cell genomics of testes. || Dynamic sex chromosome expression in Drosophila male germ cells. || Nat. Commun. || [https://pubmed.ncbi.nlm.nih.gov/33563972/ 33563972] || [https://flybase.org/reports/FBrf0248088 FBrf0248088]
 
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| FBrf0248123 || [https://pubmed.ncbi.nlm.nih.gov/33558234/ 33558234] || Proc. Natl. Acad. Sci. U.S.A. || The Krüppel-like factor Cabut has cell cycle regulatory properties similar to E2F1.||new reporter line and new null allele were generated in this paper
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| New reporter line and new null allele were generated in this paper. || The Krüppel-like factor Cabut has cell cycle regulatory properties similar to E2F1. || Proc. Natl. Acad. Sci. U.S.A. || [https://pubmed.ncbi.nlm.nih.gov/33558234/ 33558234] || [https://flybase.org/reports/FBrf0248123 FBrf0248123]
 
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| FBrf0247919 || [https://pubmed.ncbi.nlm.nih.gov/33239786/ 33239786] || Nature || Neural circuit mechanisms of sexual receptivity in Drosophila females.||split-GAL4 lines labeling specific cell types
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| Split-GAL4 lines labeling specific cell types. || Neural circuit mechanisms of sexual receptivity in Drosophila females. || Nature || [https://pubmed.ncbi.nlm.nih.gov/33239786/ 33239786] || [https://flybase.org/reports/FBrf0247919 FBrf0247919]
 
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| FBrf0248082 || [https://pubmed.ncbi.nlm.nih.gov/33495632/ 33495632] || Nat. Cell Biol. || Ribosomopathy-associated mutations cause proteotoxic stress that is alleviated by TOR inhibition.||A translational fidelity reporter (UAS-Fluc-STOP-Nluc) - Drosophila mutant strains (RPS23-R67K, RPS26-KO)
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| A translational fidelity reporter (UAS-Fluc-STOP-Nluc) - Drosophila mutant strains (RPS23-R67K, RPS26-KO). || Ribosomopathy-associated mutations cause proteotoxic stress that is alleviated by TOR inhibition.|| Nat. Cell Biol. || [https://pubmed.ncbi.nlm.nih.gov/33495632/ 33495632] || [https://flybase.org/reports/FBrf0248082 FBrf0248082]
 
|-
 
|-
| FBrf0248109 || [https://pubmed.ncbi.nlm.nih.gov/33558226/ 33558226] || Proc. Natl. Acad. Sci. U.S.A. || Multisensory interactions regulate feeding behavior in Drosophila.||The modified PER assay can deliver stimuli not only for taste, but also for other senses. we made a line that can express the hair plate in legs.
+
| The modified PER assay can deliver stimuli not only for taste, but also for other senses. We made a line that can express the hair plate in legs. || Multisensory interactions regulate feeding behavior in Drosophila.|| Proc. Natl. Acad. Sci. U.S.A. || [https://pubmed.ncbi.nlm.nih.gov/33558226/ 33558226] || [https://flybase.org/reports/FBrf0248109 FBrf0248109]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247921 || [https://pubmed.ncbi.nlm.nih.gov/33242000/ 33242000] || eLife || Magnesium efflux from Drosophila Kenyon cells is critical for normal and diet-enhanced long-term memory.||UAS-MagIC, fluorescent Mg2+ reporter transgene
+
| UAS-MagIC, fluorescent Mg2+ reporter transgene. || Magnesium efflux from Drosophila Kenyon cells is critical for normal and diet-enhanced long-term memory.|| eLife || [https://pubmed.ncbi.nlm.nih.gov/33242000/ 33242000] || [https://flybase.org/reports/FBrf0247921 FBrf0247921]
 
|-
 
|-
| FBrf0248065 || [https://pubmed.ncbi.nlm.nih.gov/33513131/ 33513131] || PLoS Comput. Biol. || Modeling invasion patterns in the glioblastoma battlefield.||Mathematical algoritjm for cytoneme/Tumor microtube expansion
+
| Mathematical algorithm for cytoneme/Tumor microtube expansion. || Modeling invasion patterns in the glioblastoma battlefield. || PLoS Comput. Biol. || [https://pubmed.ncbi.nlm.nih.gov/33513131/ 33513131] ||[https://flybase.org/reports/FBrf0248065 FBrf0248065]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247818 || [https://pubmed.ncbi.nlm.nih.gov/33444322/ 33444322] || PLoS Biol. || Versatile CRISPR/Cas9-mediated mosaic analysis by gRNA-induced crossing-over for unmodified genomes.||We developed a new technique called mosaic analysis by gRNA-induced crossing-over (MAGIC) for mosaic analysis with unmodified genomes. We developed the MAGIC toolkit for chromosomal arm 2L.
+
| We developed a new technique called mosaic analysis by gRNA-induced crossing-over (MAGIC) for mosaic analysis with unmodified genomes. We developed the MAGIC toolkit for chromosomal arm 2L. || Versatile CRISPR/Cas9-mediated mosaic analysis by gRNA-induced crossing-over for unmodified genomes. || PLoS Biol. || [https://pubmed.ncbi.nlm.nih.gov/33444322/ 33444322] || [https://flybase.org/reports/FBrf0247818 FBrf0247818]
 +
|-
 
|}
 
|}
  
Line 50: Line 155:
 
{| class="wikitable"
 
{| class="wikitable"
 
|-
 
|-
! ''FBrf number''!!''PubMed ID''!!''Journal''!!''Title''!!''Author description of technical advance''
+
! ''Author description of technical advance''!!''Title''!!''Journal''!!''PubMed ID''!! ''FBrf number''
 
|-
 
|-
| FBrf0247452 || [https://pubmed.ncbi.nlm.nih.gov/33273532/ 33273532] || Sci. Rep. || HumanaFly: high-throughput transgenesis and expression of breast cancer transcripts in Drosophila eye discovers the RPS12-Wingless signaling axis.|| Human genes expressed in breast cancer patients are screened for their ability to aberrate development of the Drosophila eye. Transgenic construct UAS-hRPS12 was described in this paper.
+
| Human genes expressed in breast cancer patients are screened for their ability to aberrate development of the Drosophila eye. Transgenic construct UAS-hRPS12 was described in this paper.|| HumanaFly: high-throughput transgenesis and expression of breast cancer transcripts in Drosophila eye discovers the RPS12-Wingless signaling axis.|| Sci. Rep. || [https://pubmed.ncbi.nlm.nih.gov/33273532/ 33273532] || [https://flybase.org/reports/FBrf0247452 FBrf0247452]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247305 || [https://pubmed.ncbi.nlm.nih.gov/33196763/ 33196763] || J. Cell Biol. || centrocortin RNA localization to centrosomes is regulated by FMRP and facilitates error-free mitosis.|| Python-based code used to quantify object-to-object distances; e.g., mRNA to centrosomes
+
| Python-based code used to quantify object-to-object distances; e.g., mRNA to centrosomes.|| centrocortin RNA localization to centrosomes is regulated by FMRP and facilitates error-free mitosis.|| J. Cell Biol. || [https://pubmed.ncbi.nlm.nih.gov/33196763/ 33196763] || [https://flybase.org/reports/FBrf0247305 FBrf0247305]
 
|-
 
|-
| FBrf0247435 || [https://pubmed.ncbi.nlm.nih.gov/32815271/ 32815271] || EMBO Rep. || A cell atlas of adult muscle precursors uncovers early events in fibre-type divergence in Drosophila.|| A single cell atlas of the proximal wing disc was built by single cell RNAseq. The myoblast, tracheal and epithelial cells associated with third instar larval wing disc were mapped. Diverse cell types along with specific markers were identified.
+
| A single cell atlas of the proximal wing disc was built by single cell RNAseq. The myoblast, tracheal and epithelial cells associated with third instar larval wing disc were mapped. Diverse cell types along with specific markers were identified. || A cell atlas of adult muscle precursors uncovers early events in fibre-type divergence in Drosophila.|| EMBO Rep.  || [https://pubmed.ncbi.nlm.nih.gov/32815271/ 32815271] || [https://flybase.org/reports/FBrf0247435 FBrf0247435]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247504 || [https://pubmed.ncbi.nlm.nih.gov/33168584/ 33168584] || Development || Recruitment of BAF to the nuclear envelope couples the LINC complex to endoreplication.|| Expansion microscopy for larval tissue
+
| Expansion microscopy for larval tissue. || Recruitment of BAF to the nuclear envelope couples the LINC complex to endoreplication. || Development || [https://pubmed.ncbi.nlm.nih.gov/33168584/ 33168584] || [https://flybase.org/reports/FBrf0247504 FBrf0247504]
 
|-
 
|-
| FBrf0247550 || [https://pubmed.ncbi.nlm.nih.gov/33321059/ 33321059] || Open Biol. || Identification of FoxP circuits involved in locomotion and object fixation in Drosophila.|| Several new fly lines. In particular: - a GFP-tagged FoxP gene - a null allele - a conditional UAS-gRNA-based knock-out line.
+
| Several new fly lines. In particular: - a GFP-tagged FoxP gene - a null allele - a conditional UAS-gRNA-based knock-out line. || Identification of FoxP circuits involved in locomotion and object fixation in Drosophila. || Open Biol || [https://pubmed.ncbi.nlm.nih.gov/33321059/ 33321059] || [https://flybase.org/reports/FBrf0247550 FBrf0247550]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0245063 || [https://pubmed.ncbi.nlm.nih.gov/31978587/ 31978587] || Insect Biochem. Mol. Biol. || Bicistronic expression and differential localization of proteins in insect cells and Drosophila suzukii using picornaviral 2A peptides.|| nuclear localization signal (NLS) that isolated from D. suzukii transformer gene
+
| Nuclear localization signal (NLS) that isolated from D. suzukii transformer gene. || Bicistronic expression and differential localization of proteins in insect cells and Drosophila suzukii using picornaviral 2A peptides. || Insect Biochem. Mol. Biol. ||  [https://pubmed.ncbi.nlm.nih.gov/31978587/ 31978587] || [https://flybase.org/reports/FBrf0245063 FBrf0245063]
 
|-
 
|-
| FBrf0247583 || [https://pubmed.ncbi.nlm.nih.gov/33339500/ 33339500] || BMC Genet. || Identification and characterization of four Drosophila suzukii cellularization genes and their promoters.|| piggyBac constructs that express DeRed at embryonic stage
+
| piggyBac constructs that express DeRed at embryonic stage. || Identification and characterization of four Drosophila suzukii cellularization genes and their promoters. || BMC Genet. || [https://pubmed.ncbi.nlm.nih.gov/33339500/ 33339500] || [https://flybase.org/reports/FBrf0247583 FBrf0247583]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247622 || [https://pubmed.ncbi.nlm.nih.gov/33377013/ 33377013] || STAR Protoc || Protocol for a Binary Choice Feeding Assay Using Adult, Axenic Drosophila.|| The protocol describes preparation of adult axenic Drosophila before monitoring their behavior in a two-choice feeding assay, where flies are confronted with an axenic versus a dead or alive bacteria-contaminated feeding solution.
+
| The protocol describes preparation of adult axenic Drosophila before monitoring their behavior in a two-choice feeding assay, where flies are confronted with an axenic versus a dead or alive bacteria-contaminated feeding solution. || Protocol for a Binary Choice Feeding Assay Using Adult, Axenic Drosophila.|| STAR Protoc || [https://pubmed.ncbi.nlm.nih.gov/33377013/ 33377013] || [https://flybase.org/reports/FBrf0247622 FBrf0247622]
 
|-
 
|-
| FBrf0247664 || [https://pubmed.ncbi.nlm.nih.gov/33320085/ 33320085] || eLife || A genome engineering resource to uncover principles of cellular organization and tissue architecture by lipid signaling.|| CRISPR dual-gRNA transgenic targeting phosphoinositide signaling genes
+
| CRISPR dual-gRNA transgenic targeting phosphoinositide signaling genes. || A genome engineering resource to uncover principles of cellular organization and tissue architecture by lipid signaling. || eLife || [https://pubmed.ncbi.nlm.nih.gov/33320085/ 33320085] || [https://flybase.org/reports/FBrf0247664 FBrf0247664]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247494 || [https://pubmed.ncbi.nlm.nih.gov/33171098/ 33171098] || Dev. Cell ||Lineage-Resolved Enhancer and Promoter Usage during a Time Course of Embryogenesis.|| Tissue- and time-resolved chromatin accessibility during Drosophila embryogenesis
+
| Tissue- and time-resolved chromatin accessibility during Drosophila embryogenesis. ||Lineage-Resolved Enhancer and Promoter Usage during a Time Course of Embryogenesis. || Dev. Cell || [https://pubmed.ncbi.nlm.nih.gov/33171098/ 33171098] || [https://flybase.org/reports/FBrf0247494 FBrf0247494]
 
|-
 
|-
| FBrf0247517 || [https://pubmed.ncbi.nlm.nih.gov/33262328/ 33262328] || Nat. Commun. ||Deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure.|| We apply deep learning on thousands of mRNA datasets to examine the genetic regulatory code controlling mRNA abundance in model organisms including Drosophila melanogaster, and show that in all organisms mRNA abundance can be predicted directly from DNA sequence.
+
| We apply deep learning on thousands of mRNA datasets to examine the genetic regulatory code controlling mRNA abundance in model organisms including Drosophila melanogaster, and show that in all organisms mRNA abundance can be predicted directly from DNA sequence. ||Deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure. || Nat. Commun. ||  [https://pubmed.ncbi.nlm.nih.gov/33262328/ 33262328] || [https://flybase.org/reports/FBrf0247517 FBrf0247517]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247546 || [https://pubmed.ncbi.nlm.nih.gov/33112725/ 33112725] || Mol. Biol. Cell ||ESCargo: a regulatable fluorescent secretory cargo for diverse model organisms.|| UAS-driven regulatable fluorescent secretory cargo
+
| UAS-driven regulatable fluorescent secretory cargo.] ||ESCargo: a regulatable fluorescent secretory cargo for diverse model organisms. || Mol. Biol. Cell || [https://pubmed.ncbi.nlm.nih.gov/33112725/ 33112725] || [https://flybase.org/reports/FBrf0247546 FBrf0247546]
 
|-
 
|-
| FBrf0247672 || [https://pubmed.ncbi.nlm.nih.gov/33337563/ 33337563] || FASEB J. ||Regulatory mechanism of daily sleep by miR-276a.|| 1. S2 cell culture and luciferase reporter assay; 2. AGO1 immunoprecipitation (AGO1 IP); 3. Immunofluorescence experiments;
+
| 1. S2 cell culture and luciferase reporter assay; 2. AGO1 immunoprecipitation (AGO1 IP); 3. Immunofluorescence experiments. ||Regulatory mechanism of daily sleep by miR-276a. || FASEB J. || [https://pubmed.ncbi.nlm.nih.gov/33337563/ 33337563] || [https://flybase.org/reports/FBrf0247672 FBrf0247672]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247745 || [https://pubmed.ncbi.nlm.nih.gov/33319644/ 33319644] || Fly ||PseudoBase: a genomic visualization and exploration resource for the Drosophila pseudoobscura subgroup.|| Resource: website for downloading aligned genome sequences from Drosophila pseudoobscura species group
+
| Resource: website for downloading aligned genome sequences from Drosophila pseudoobscura species group. ||PseudoBase: a genomic visualization and exploration resource for the Drosophila pseudoobscura subgroup. || Fly || [https://pubmed.ncbi.nlm.nih.gov/33319644/ 33319644] || [https://flybase.org/reports/FBrf0247745 FBrf0247745]
 
|-
 
|-
| FBrf0247752 || [https://pubmed.ncbi.nlm.nih.gov/33131172/ 33131172] || Insect Mol. Biol. ||Regulation of circadian behavioural output via clock-responsive miR-276b.|| S2 cell culture and luciferase reporter assay; AGO1 immunoprecipitation
+
| S2 cell culture and luciferase reporter assay; AGO1 immunoprecipitation. ||Regulation of circadian behavioural output via clock-responsive miR-276b.|| Insect Mol. Biol.  || [https://pubmed.ncbi.nlm.nih.gov/33131172/ 33131172] || [https://flybase.org/reports/FBrf0247752 FBrf0247752]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247665 || [https://pubmed.ncbi.nlm.nih.gov/33234716/ 33234716] || Development ||Postsynaptic cAMP signalling regulates the antagonistic balance of Drosophila glutamate receptor subtypes.|| superresolution imaging of glutamate receptors were obtained with structured illumination microscopy (SIM)
+
| Superresolution imaging of glutamate receptors were obtained with structured illumination microscopy (SIM). ||Postsynaptic cAMP signalling regulates the antagonistic balance of Drosophila glutamate receptor subtypes.|| Development || [https://pubmed.ncbi.nlm.nih.gov/33234716/ 33234716] || [https://flybase.org/reports/FBrf0247665 FBrf0247665]
 
|-
 
|-
| FBrf0247675 || [https://pubmed.ncbi.nlm.nih.gov/33077913/ 33077913] || Nat. Genet. ||Regulation of single-cell genome organization into TADs and chromatin nanodomains.|| Characterization of novel chromosomal structures in Drosophila embryonic cells, by combining 3D structured illumination microscopy (3D-SIM) and DAPI or FISH staining with a X Oligopaint probe (observation in a haploid context in sorted male embryos using a Y-GFP line). Ext. Fig.6
+
| Characterization of novel chromosomal structures in Drosophila embryonic cells, by combining 3D structured illumination microscopy (3D-SIM) and DAPI or FISH staining with a X Oligopaint probe (observation in a haploid context in sorted male embryos using a Y-GFP line). Ext. Fig.6. ||Regulation of single-cell genome organization into TADs and chromatin nanodomains.  || Nat. Genet. || [https://pubmed.ncbi.nlm.nih.gov/33077913/ 33077913] || [https://flybase.org/reports/FBrf0247675 FBrf0247675]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247770 || [https://pubmed.ncbi.nlm.nih.gov/33437967/ 33437967] || STAR Protoc ||X-ray fluorescence microscopy scanning of Drosophila oocytes and eggs.|| The methods paper describes detailed procedure for X-ray fluorescence microscopy scanning of Drosophila oocytes and eggs to measure elemental distribution. Our report on the elemental distributions themselves was published in Hu et al. iScience 2020.
+
| The methods paper describes detailed procedure for X-ray fluorescence microscopy scanning of Drosophila oocytes and eggs to measure elemental distribution. Our report on the elemental distributions themselves was published in Hu et al. iScience 2020. ||X-ray fluorescence microscopy scanning of Drosophila oocytes and eggs. || STAR Protoc || [https://pubmed.ncbi.nlm.nih.gov/33437967/ 33437967] || [https://flybase.org/reports/FBrf0247770 FBrf0247770]
 
|}
 
|}
  
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{| class="wikitable"
 
{| class="wikitable"
 
|-
 
|-
! ''FBrf number''!!''PubMed ID''!!''Journal''!!''Title''!!''Author description of technical advance''
+
! ''Author description of technical advance''!!''Title''!!''Journal''!!''PubMed ID''!! ''FBrf number''
 
|-
 
|-
| FBrf0247159 || [https://pubmed.ncbi.nlm.nih.gov/32917721/ 32917721] || G3 (Bethesda) || Analysis of Gal4 Expression Patterns in Adult Drosophila Females. || Analysis of Gal4 expression patterns of commonly used Gal4 drivers in adult females.
+
| Analysis of Gal4 expression patterns of commonly used Gal4 drivers in adult females. || Analysis of Gal4 Expression Patterns in Adult Drosophila Females. || G3 (Bethesda)  || [https://pubmed.ncbi.nlm.nih.gov/32917721/ 32917721] || [https://flybase.org/reports/FBrf0247159 FBrf0247159]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247182 || [https://pubmed.ncbi.nlm.nih.gov/33060173/ 33060173] || Genome Res. || Active retrotransposons help maintain pericentromeric heterochromatin required for faithful cell division. || We defined the origins of repeat-derived RNAs and their specific chromatin locations in Drosophila S2 cells using the global RNA–DNA interaction sequencing  method(GRID-seq).
+
| We defined the origins of repeat-derived RNAs and their specific chromatin locations in Drosophila S2 cells using the global RNA–DNA interaction sequencing  method (GRID-seq). || Active retrotransposons help maintain pericentromeric heterochromatin required for faithful cell division. || Genome Res. || [https://pubmed.ncbi.nlm.nih.gov/33060173/ 33060173] || [https://flybase.org/reports/FBrf0247182 FBrf0247182]
 
|-
 
|-
| FBrf0247192 || [https://pubmed.ncbi.nlm.nih.gov/33168136/ 33168136] || eLife || The Drosophila Individual Activity Monitoring and Detection System (DIAMonDS). || We have developed a novel automated Drosophila life cycle multi-phase transition  (pupariation, eclosion, and death) timing detection and measurement system with high accuracy and high temporal resolution.
+
| We have developed a novel automated Drosophila life cycle multi-phase transition  (pupariation, eclosion, and death) timing detection and measurement system with high accuracy and high temporal resolution. ||The Drosophila Individual Activity Monitoring and Detection System (DIAMonDS). || eLife || [https://pubmed.ncbi.nlm.nih.gov/33168136/ 33168136] ||  [https://flybase.org/reports/FBrf0247192 FBrf0247192]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247218 || [https://pubmed.ncbi.nlm.nih.gov/33176146/ 33176146] ||Cell Rep.  || Intramacrophage ROS Primes the Innate Immune System via JAK/STAT and Toll Activation. || A hydrogen peroxide probe was detected in vivo through a burnt fluorescent probe (TCFB, 2-Dicyanomethylene-3-cyano-4,5,5-trimethyl-2,5-dihydrofuran) [Sedgwick et al., 2017].
+
| A hydrogen peroxide probe was detected in vivo through a burnt fluorescent probe (TCFB, 2-Dicyanomethylene-3-cyano-4,5,5-trimethyl-2,5-dihydrofuran) (Sedgwick et al., 2017). || Intramacrophage ROS Primes the Innate Immune System via JAK/STAT and Toll Activation. ||Cell Rep.  || [https://pubmed.ncbi.nlm.nih.gov/33176146/ 33176146] || [https://flybase.org/reports/FBrf0247218 FBrf0247218]
 
|-
 
|-
| FBrf0247316 || [https://pubmed.ncbi.nlm.nih.gov/33113043/ 33113043] || Apoptosis || Functional characterization of the Drosophila suzukii pro-apoptotic genes reaper, head involution defective and grim. || The binary expression of different pro-apoptotic genes using 2A peptides.
+
| The binary expression of different pro-apoptotic genes using 2A peptides. || Functional characterization of the Drosophila suzukii pro-apoptotic genes reaper, head involution defective and grim. || Apoptosis || [https://pubmed.ncbi.nlm.nih.gov/33113043/ 33113043] || [https://flybase.org/reports/FBrf0247316 FBrf0247316]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247326 || [https://pubmed.ncbi.nlm.nih.gov/33016195/ 33016195] || Fly || A pipeline for precise and efficient genome editing by sgRNA-Cas9 RNPs in Drosophila. || Improved pipeline for CRISPR mediated genome editing in Drosophila species. Generation of new vector to make donor plasmids for homology-directed repair
+
| Improved pipeline for CRISPR mediated genome editing in Drosophila species. Generation of new vector to make donor plasmids for homology-directed repair. || A pipeline for precise and efficient genome editing by sgRNA-Cas9 RNPs in Drosophila. ||Fly || [https://pubmed.ncbi.nlm.nih.gov/33016195/ 33016195] || [https://flybase.org/reports/FBrf0247326 FBrf0247326]
 
|-
 
|-
| FBrf0247327 || [https://pubmed.ncbi.nlm.nih.gov/33234068/ 33234068] || Open Biol. || The application of rapid evaporative ionization mass spectrometry in the analysis of Drosophila species-a potential new tool in entomology. || We describe a novel high throughput mass spectrometry approach to identifying species and sex by their metabolites. We show it works invertebrates generally, and can accurately distinguish closely related Drosophila (e.g. melanogaster and simulans) with potential for mass scoring
+
| We describe a novel high throughput mass spectrometry approach to identifying species and sex by their metabolites. We show it works invertebrates generally, and can accurately distinguish closely related Drosophila (e.g. melanogaster and simulans) with potential for mass scoring. || The application of rapid evaporative ionization mass spectrometry in the analysis of Drosophila species-a potential new tool in entomology. || Open Biol.  || [https://pubmed.ncbi.nlm.nih.gov/33234068/ 33234068] || [https://flybase.org/reports/FBrf0247327 FBrf0247327]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247119 || [https://pubmed.ncbi.nlm.nih.gov/32973040/ 32973040] || Genome Res. || Transposon expression in the Drosophila brain is driven by neighboring genes and diversifies the neural transcriptome. || Here we introduce TEchim, a new software that extracts chimeric sequencing reads that span transposon-gene breakpoints. In addition, we introduce scHardyWeinberg, a new approach to quantify co-expression levels in high-throughput single-cell sequencing data.
+
| Here we introduce TEchim, a new software that extracts chimeric sequencing reads that span transposon-gene breakpoints. In addition, we introduce scHardyWeinberg, a new approach to quantify co-expression levels in high-throughput single-cell sequencing data. ||Transposon expression in the Drosophila brain is driven by neighboring genes and diversifies the neural transcriptome. || Genome Res.  || [https://pubmed.ncbi.nlm.nih.gov/32973040/ 32973040] || [https://flybase.org/reports/FBrf0247119 FBrf0247119]
 
|-
 
|-
| FBrf0247148 || [https://pubmed.ncbi.nlm.nih.gov/33159074/ 33159074] || Nat. Commun. || A single-cell atlas and lineage analysis of the adult Drosophila ovary. || Single-cell RNA-sequencing dataset of the adult Drosophila ovary containing transcriptome profiles for all major ovarian cell types.
+
| Single-cell RNA-sequencing dataset of the adult Drosophila ovary containing transcriptome profiles for all major ovarian cell types. || A single-cell atlas and lineage analysis of the adult Drosophila ovary. || Nat. Commun.|| [https://pubmed.ncbi.nlm.nih.gov/33159074/ 33159074] || [https://flybase.org/reports/FBrf0247148 FBrf0247148]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247254 || [https://pubmed.ncbi.nlm.nih.gov/33184447/ 33184447] || Commun. Biol. || A sensitive mNeonGreen reporter system to measure transcriptional dynamics in Drosophila development. || We developed an optimized version of the bright and fast-maturing fluorescent protein mNeonGreen to serve as a real-time, quantitative reporter of gene/enhancer expression.  
+
| We developed an optimized version of the bright and fast-maturing fluorescent protein mNeonGreen to serve as a real-time, quantitative reporter of gene/enhancer expression. || A sensitive mNeonGreen reporter system to measure transcriptional dynamics in Drosophila development. || Commun. Biol. || [https://pubmed.ncbi.nlm.nih.gov/33184447/ 33184447] || [https://flybase.org/reports/FBrf0247254 FBrf0247254]
 
|-
 
|-
| FBrf0247413 || [https://pubmed.ncbi.nlm.nih.gov/33274326/ 33274326] || Micropub Biol || Evidence of slightly increased Pol II pausing in UPF1-depleted Drosophila melanogaster cells. || DRB treatment followed by Pol II ChIP
+
| DRB treatment followed by Pol II ChIP. || Evidence of slightly increased Pol II pausing in UPF1-depleted Drosophila melanogaster cells. || Micropub Biol || [https://pubmed.ncbi.nlm.nih.gov/33274326/ 33274326] || [https://flybase.org/reports/FBrf0247413 FBrf0247413]
 
|}
 
|}
  
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{| class="wikitable"
 
{| class="wikitable"
 
|-
 
|-
! ''FBrf number''!!''PubMed ID''!!''Journal''!!''Title''!!''Author description of technical advance''
+
! ''Author description of technical advance''!!''Title''!!''Journal''!!''PubMed ID''!! ''FBrf number''
 
|-
 
|-
| FBrf0246918 || [https://pubmed.ncbi.nlm.nih.gov/32955431/ 32955431] || eLife || AANAT1 functions in astrocytes to regulate sleep homeostasis. || Antibody
+
| Antibody. || AANAT1 functions in astrocytes to regulate sleep homeostasis. || eLife  || [https://pubmed.ncbi.nlm.nih.gov/32955431/ 32955431] || [https://flybase.org/reports/FBrf0246918 FBrf0246918]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0246897 || [https://pubmed.ncbi.nlm.nih.gov/33036271/ 33036271] || Biomedicines || Humanization of Drosophila Gαo to Model GNAO1 Paediatric Encephalopathies. || Endogenous locus was edited with a two-step CRISPR/Cas9-mediated replacement.
+
| Endogenous locus was edited with a two-step CRISPR/Cas9-mediated replacement. || Humanization of Drosophila Gαo to Model GNAO1 Paediatric Encephalopathies. || Biomedicines || [https://pubmed.ncbi.nlm.nih.gov/33036271/ 33036271] || [https://flybase.org/reports/FBrf0246897 FBrf0246897]
 
|-
 
|-
| FBrf0246907 || [https://pubmed.ncbi.nlm.nih.gov/32917765/ 32917765] || Biol. Open || Quantifying Drosophila adults with the use of a smartphone. || We optimized, tested, and introduced a new method of automated count of Drosophila adults using the SeedCounter mobile application. The application is available on all mobile devices based on the Android system, and it does not require any additional equipment.
+
| We optimized, tested, and introduced a new method of automated count of Drosophila adults using the SeedCounter mobile application. The application is available on all mobile devices based on the Android system, and it does not require any additional equipment. || Quantifying Drosophila adults with the use of a smartphone.  || Biol. Open || [https://pubmed.ncbi.nlm.nih.gov/32917765/ 32917765] || [https://flybase.org/reports/FBrf0246907 FBrf0246907]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0246919 || [https://pubmed.ncbi.nlm.nih.gov/32783958/ 32783958] || J. Insect Physiol. || How to use the development of individual Drosophila larvae as a metabolic sensor. || We introduce a developmental 96-well plate assay to use individual Drosophila larvae as tool for metabolic studies.
+
| We introduce a developmental 96-well plate assay to use individual Drosophila larvae as tool for metabolic studies. || How to use the development of individual Drosophila larvae as a metabolic sensor. || J. Insect Physiol.  || [https://pubmed.ncbi.nlm.nih.gov/32783958/ 32783958] || [https://flybase.org/reports/FBrf0246919 FBrf0246919]
 
|-
 
|-
| FBrf0247073 || [https://pubmed.ncbi.nlm.nih.gov/33077914/ 33077914] || Nat. Genet. || CHESS enables quantitative comparison of chromatin contact data and automatic feature extraction. ||Novel method to compare 3D chromatin conformation data in Drosophila
+
| Novel method to compare 3D chromatin conformation data in Drosophila. || CHESS enables quantitative comparison of chromatin contact data and automatic feature extraction. || Nat. Genet.  || [https://pubmed.ncbi.nlm.nih.gov/33077914/ 33077914] ||[https://flybase.org/reports/FBrf0247073 FBrf0247073]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247109 || [https://pubmed.ncbi.nlm.nih.gov/33443210/ 33443210]32814018 || Neuron || Synthesis of Conserved Odor Object Representations in a Random, Divergent-Convergent Network. ||Comprehensive calcium imaging from all 2,000 Kenyon cells in the mushroom body at single cell resolution.
+
| Comprehensive calcium imaging from all 2,000 Kenyon cells in the mushroom body at single cell resolution. || Synthesis of Conserved Odor Object Representations in a Random, Divergent-Convergent Network. || Neuron  || [https://pubmed.ncbi.nlm.nih.gov/32814018/ 32814018] ||[https://flybase.org/reports/FBrf0247109 FBrf0247109]
 
|-
 
|-
| FBrf0247160 || [https://pubmed.ncbi.nlm.nih.gov/33155978/ 33155978] || eLife || Modulation of flight and feeding behaviours requires presynaptic IP3Rs in dopaminergic neurons. ||Dominant negative form of IP3R protein. It has three mutated amino acids which prevent ligand binding. IP3R being tetramer, requires IP3 binding to all monomers. Hence presence of even single IP3R-DN monomer in tetramer can render whole IP3R protein complex functionless.
+
| Dominant negative form of IP3R protein. It has three mutated amino acids which prevent ligand binding. IP3R being tetramer, requires IP3 binding to all monomers. Hence presence of even single IP3R-DN monomer in tetramer can render whole IP3R protein complex functionless. || Modulation of flight and feeding behaviours requires presynaptic IP3Rs in dopaminergic neurons. || eLife  || [https://pubmed.ncbi.nlm.nih.gov/33155978/ 33155978] ||[https://flybase.org/reports/FBrf0247160 FBrf0247160]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247169 || [https://pubmed.ncbi.nlm.nih.gov/32916115/ 32916115] || Curr. Biol. || Collective Cell Sorting Requires Contractile Cortical Waves in Germline Cells. ||use of Hydrogel for live-imaging of Drosophila ovaries
+
| Use of Hydrogel for live-imaging of Drosophila ovaries. || Collective Cell Sorting Requires Contractile Cortical Waves in Germline Cells. || Curr. Biol.|| [https://pubmed.ncbi.nlm.nih.gov/32916115/ 32916115] || [https://flybase.org/reports/FBrf0247169 FBrf0247169]
 
|-
 
|-
| FBrf0247175 || [https://pubmed.ncbi.nlm.nih.gov/33048531/ 33048531] || Anal. Chem. || Real-Time Measurement of Stimulated Dopamine Release in Compartments of the Adult Drosophila melanogaster Mushroom Body. ||This paper uses fast-scan cyclic voltammetry at a carbon-fiber microelectrode to make real-time measurement of stimulated endogenous dopamine release in the mushroom body of adult Drosophila brains using various stimulation techniques
+
| This paper uses fast-scan cyclic voltammetry at a carbon-fiber microelectrode to make real-time measurement of stimulated endogenous dopamine release in the mushroom body of adult Drosophila brains using various stimulation techniques. || Real-Time Measurement of Stimulated Dopamine Release in Compartments of the Adult Drosophila melanogaster Mushroom Body. || Anal. Chem. || [https://pubmed.ncbi.nlm.nih.gov/33048531/ 33048531] ||[https://flybase.org/reports/FBrf0247175 FBrf0247175]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247184 || [https://pubmed.ncbi.nlm.nih.gov/33163946/ 33163946] || iScience || Transcription Factor Binding Affinities and DNA Shape Readout.||New measurements of Position weight Matrices (PWMs) Dinucleotide Position weight Matrices (DPWMs) for 13 Drosophila transcription factors and their DNA shape analysis for all shape features.
+
| New measurements of Position weight Matrices (PWMs) Dinucleotide Position weight Matrices (DPWMs) for 13 Drosophila transcription factors and their DNA shape analysis for all shape features. || Transcription Factor Binding Affinities and DNA Shape Readout. || iScience || [https://pubmed.ncbi.nlm.nih.gov/33163946/ 33163946] || [https://flybase.org/reports/FBrf0247184 FBrf0247184]
 
|-
 
|-
| FBrf0247019 || [https://pubmed.ncbi.nlm.nih.gov/33108408/ 33108408] || PLoS ONE || Three distinct mechanisms, Notch instructive, permissive, and independent, regulate the expression of two different pericardial genes to specify cardiac cell subtypes.||Sequence, features, and schematic of the pWattB-nlacZ reporter construct vector
+
| Sequence, features, and schematic of the pWattB-nlacZ reporter construct vector. || Three distinct mechanisms, Notch instructive, permissive, and independent, regulate the expression of two different pericardial genes to specify cardiac cell subtypes. || PLoS ONE.|| [https://pubmed.ncbi.nlm.nih.gov/33108408/ 33108408] || [https://flybase.org/reports/FBrf0247019 FBrf0247019]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247101 || [https://pubmed.ncbi.nlm.nih.gov/33117817/ 33117817] || Front. Cell Dev. Biol. || An Immobilization Technique for Long-Term Time-Lapse Imaging of Explanted Drosophila Tissues.||A new method for immobilizing explanted Drosophila tissue in agarose for use in long-term live imaging.
+
| A new method for immobilizing explanted Drosophila tissue in agarose for use in long-term live imaging. || An Immobilization Technique for Long-Term Time-Lapse Imaging of Explanted Drosophila Tissues. || Front. Cell Dev. Biol. || [https://pubmed.ncbi.nlm.nih.gov/33117817/ 33117817] || [https://flybase.org/reports/FBrf0247101 FBrf0247101]
 
|-
 
|-
| FBrf0247149 || [https://pubmed.ncbi.nlm.nih.gov/32955048/ 32955048] || Analyst || Improving serotonin fast-scan cyclic voltammetry detection: new waveforms to reduce electrode fouling.||Using new fast-scan cyclic voltammetry serotonin specific waveforms for in vivo detection of serotonin in Drosophila tissue.
+
| Using new fast-scan cyclic voltammetry serotonin specific waveforms for in vivo detection of serotonin in Drosophila tissue. || Improving serotonin fast-scan cyclic voltammetry detection: new waveforms to reduce electrode fouling. || Analyst
 +
|| [https://pubmed.ncbi.nlm.nih.gov/32955048/ 32955048] ||[https://flybase.org/reports/FBrf0247149 FBrf0247149]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247179 || [https://pubmed.ncbi.nlm.nih.gov/33090988/ 33090988] || PLoS Biol. || Interphase-arrested Drosophila embryos activate zygotic gene expression and initiate mid-blastula transition events at a low nuclear-cytoplasmic ratio.||We have developed a new protocol to indcue cell cycle arrest in early embryos, and deposited RNA-seq data for WT embryos and embryos arrested in cycle 12 for differernt amount of time.
+
| We have developed a new protocol to indcue cell cycle arrest in early embryos, and deposited RNA-seq data for WT embryos and embryos arrested in cycle 12 for differernt amount of time. || Interphase-arrested Drosophila embryos activate zygotic gene expression and initiate mid-blastula transition events at a low nuclear-cytoplasmic ratio. || PLoS Biol.|| [https://pubmed.ncbi.nlm.nih.gov/33090988/ 33090988] || [https://flybase.org/reports/FBrf0247179 FBrf0247179]
 
|-
 
|-
| FBrf0247228 || [https://pubmed.ncbi.nlm.nih.gov/31960114/ 31960114] || Cell. Molec. Life Sci. || Loss of function in the Drosophila clock gene period results in altered intermediary lipid metabolism and increased susceptibility to starvation.||Analysis of the chronometabolome including lipids
+
| Analysis of the chronometabolome including lipids. || Loss of function in the Drosophila clock gene period results in altered intermediary lipid metabolism and increased susceptibility to starvation. || Cell. Molec. Life Sci.|| [https://pubmed.ncbi.nlm.nih.gov/31960114/ 31960114] || [https://flybase.org/reports/FBrf0247228 FBrf0247228]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| FBrf0247230 || [https://pubmed.ncbi.nlm.nih.gov/33177090/ 33177090] || Sci. Adv. || Persistent epigenetic reprogramming of sweet taste by diet.||Transgenic Targeted DamID construct for the gene polycomb-like (Pcl) under the control of a UAS.
+
| Transgenic Targeted DamID construct for the gene polycomb-like (Pcl) under the control of a UAS. || Persistent epigenetic reprogramming of sweet taste by diet. || Sci. Adv. || [https://pubmed.ncbi.nlm.nih.gov/33177090/ 33177090] || [https://flybase.org/reports/FBrf0247230 FBrf0247230]
 
|}
 
|}
  
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{| class="wikitable"
 
{| class="wikitable"
 
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! ''FBrf number''!!''PubMed ID''!!''Journal''!!''Title''!!''Author description of technical advance''
+
! ''Author description of technical advance''!!''Title''!!''Journal''!!''PubMed ID''!! ''FBrf number''
 
|-
 
|-
| [https://flybase.org/reports/FBrf0246799 FBrf0246799] || 32013401 || Biochemistry || Subverting Hedgehog Protein Autoprocessing by Chemical Induction of Paracatalysis. || Small molecules called "HACs" alter normal autoprocessing activity of hedgehog precursor protein.  Instead of reacting with cholesterol (cholesterolysis), the HACs alter hedgehog precursor autoprocessing toward a side reaction with water (hydrolysis)
+
| Small molecules called "HACs" alter normal autoprocessing activity of hedgehog precursor protein.  Instead of reacting with cholesterol (cholesterolysis), the HACs alter hedgehog precursor autoprocessing toward a side reaction with water (hydrolysis). || Subverting Hedgehog Protein Autoprocessing by Chemical Induction of Paracatalysis. || Biochemistry || [https://pubmed.ncbi.nlm.nih.gov/32013401/ 32013401] || [https://flybase.org/reports/FBrf0246799 FBrf0246799]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| [https://flybase.org/reports/FBrf0246922 FBrf0246922] || 32901612 || eLife || Topology-driven protein-protein interaction network analysis detects genetic sub-networks regulating reproductive capacity. || This paper shows how computational network analyses based on protein-protein interactions can be used to augment genetic screens to identify genes involved in essential developmental processes. The code are deposited in GitHub https://github.com/extavourlab/hpo_ova_eggL_screen.
+
| This paper shows how computational network analyses based on protein-protein interactions can be used to augment genetic screens to identify genes involved in essential developmental processes. The code are deposited in GitHub https://github.com/extavourlab/hpo_ova_eggL_screen. || Topology-driven protein-protein interaction network analysis detects genetic sub-networks regulating reproductive capacity.  || eLife || [https://pubmed.ncbi.nlm.nih.gov/32901612/ 32901612] || [https://flybase.org/reports/FBrf0246922 FBrf0246922]
 
|-
 
|-
| [https://flybase.org/reports/FBrf0246250 FBrf0246250] || 32652492 || iScience || PhotoGal4: A Versatile Light-Dependent Switch for Spatiotemporal Control of Gene Expression in Drosophila Explants.|| PhotoGal4 is a phytochrome B-based optogenetic switch for fine tuned spatiotemporal control of gene expression in Drosophila explants. PhotoGal4 activates and deactivates gene expression upon red- or far-red-light irradiation.
+
| PhotoGal4 is a phytochrome B-based optogenetic switch for fine tuned spatiotemporal control of gene expression in Drosophila explants. PhotoGal4 activates and deactivates gene expression upon red- or far-red-light irradiation. || PhotoGal4: A Versatile Light-Dependent Switch for Spatiotemporal Control of Gene Expression in Drosophila Explants. || iScience || [https://pubmed.ncbi.nlm.nih.gov/32652492/ 32652492] || [https://flybase.org/reports/FBrf0246250 FBrf0246250]
 
|- bgcolor="lightgrey"
 
|- bgcolor="lightgrey"
| [https://flybase.org/reports/FBrf0246808 FBrf0246808] || 32973185 || Sci. Rep. || A novel setup for simultaneous two-photon functional imaging and precise spectral and spatial visual stimulation in Drosophila.|| We developed a unique visual stimulation setup to probe spectral, spatial, & temporal properties using neural activity imaging. Custom optical filters enabled simultaneous two-photon imaging & visual stimulation over a wide range of hues without compromising the temporal rates.
+
| We developed a unique visual stimulation setup to probe spectral, spatial, & temporal properties using neural activity imaging. Custom optical filters enabled simultaneous two-photon imaging & visual stimulation over a wide range of hues without compromising the temporal rates. || A novel setup for simultaneous two-photon functional imaging and precise spectral and spatial visual stimulation in Drosophila. || Sci. Rep.  || [https://pubmed.ncbi.nlm.nih.gov/32973185/ 32973185] || [https://flybase.org/reports/FBrf0246808 FBrf0246808]
 
|-
 
|-
| [https://flybase.org/reports/FBrf0246889 FBrf0246889] || 32745561 || J. Insect Physiol. || CRISPR/Cas9 mediated disruption of the white gene leads to pigmentation deficiency and copulation failure in Drosophila suzukii.|| New white gene mutant strains were generated in Drosophila suzukii and can be used as resources to study the corresponding phenotype.  
+
| New white gene mutant strains were generated in Drosophila suzukii and can be used as resources to study the corresponding phenotype. || CRISPR/Cas9 mediated disruption of the white gene leads to pigmentation deficiency and copulation failure in Drosophila suzukii. || J. Insect Physiol. || [https://pubmed.ncbi.nlm.nih.gov/32745561/ 32745561] || [https://flybase.org/reports/FBrf0246889 FBrf0246889]
 
|- bgcolor="lightgrey"
 
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| [https://flybase.org/reports/FBrf0246845 FBrf0246845] || 32958931 || Nat. Protoc. || CRISPR-based engineering of gene knockout cells by homology-directed insertion in polyploid Drosophila S2R+ cells.|| This protocol allows generation of homozygous mutant cell lines using an insertion cassette which autocatalytically generates insertion mutations in all alleles. Knockout cells generated using this method can be directly identified by PCR without a need for DNA sequencing.
+
| This protocol allows generation of homozygous mutant cell lines using an insertion cassette which autocatalytically generates insertion mutations in all alleles. Knockout cells generated using this method can be directly identified by PCR without a need for DNA sequencing. || CRISPR-based engineering of gene knockout cells by homology-directed insertion in polyploid Drosophila S2R+ cells. || Nat. Protoc. || [https://pubmed.ncbi.nlm.nih.gov/32958931/ 32958931] || [https://flybase.org/reports/FBrf0246845 FBrf0246845]
 
|-
 
|-
| [https://flybase.org/reports/FBrf0246864 FBrf0246864] || 32759315 || J. Virol. || Partitiviruses Infecting Drosophila melanogaster and Aedes aegypti Exhibit Efficient Biparental Vertical Transmission.|| Drosophila melanogaster line infected only with galbut virus (FoCo-17 line 30)
+
| Drosophila melanogaster line infected only with galbut virus (FoCo-17 line 30). || Partitiviruses Infecting Drosophila melanogaster and Aedes aegypti Exhibit Efficient Biparental Vertical Transmission. || J. Virol.  || [https://pubmed.ncbi.nlm.nih.gov/32759315/ 32759315] || [https://flybase.org/reports/FBrf0246864 FBrf0246864]
 
|- bgcolor="lightgrey"
 
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| [https://flybase.org/reports/FBrf0246967 FBrf0246967] || 33064752 || PLoS ONE || Comparative proteomics analysis of dietary restriction in Drosophila.|| The isobaric tags for relative and absolute quantification (iTRAQ) technology was chosen to sequence the proteomes of Drosophila
+
| The isobaric tags for relative and absolute quantification (iTRAQ) technology was chosen to sequence the proteomes of Drosophila. || Comparative proteomics analysis of dietary restriction in Drosophila. || PLoS ONE|| [https://pubmed.ncbi.nlm.nih.gov/33064752/ 33064752] || [https://flybase.org/reports/FBrf0246967 FBrf0246967]
 
|}
 
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Overview

Authors of the papers listed below suggest that they include a technical advance, new type of reagent, or resource likely to be useful for other researchers. Author suggestions have been collected via the Fast-Track Your Paper tool since October 2020, with those most recently submitted at the top. Please note, there will be a lag time before listed papers can be found on FlyBase (FBrf links will become active when available) and the submission date does not necessarily match the publication date of the paper.

Technical Advances

2021

May 2021

Author description of technical advance Title Journal PubMed ID FBrf number
Quantitative analysis of parkin-dependent mitophagy using confocal microscopy 3D quantification of autophagy activation and autophagosome-to-mitochondria recruitment in a Drosophila model of Parkinson's disease. STAR Protoc 33851139 FBrf0248763
Seahorse experiments on cardiac tissue Fat-body brummer lipase determines survival and cardiac function during starvation in Drosophila melanogaster. iScience 33889813 FBrf0248791
Development of proteomics of protein trafficking Proteomics of protein trafficking by in vivo tissue-specific labeling. Nat. Commun. 33888706 FBrf0248752
Antibodies generated for AIF and DNase II DNase II mediates a parthanatos-like developmental cell death pathway in Drosophila primordial germ cells. Nat. Commun. 33863891 FBrf0248742
A novel Drosophila model for mild traumatic brain injury for investigation of lifelong brain deficits and degeneration, it also has a new imaging-based approach for analyzing brain pathology in whole mount brains. Repetitive mild head trauma induces activity mediated lifelong brain deficits in a novel Drosophila model. Sci. Rep. 33958652 FBrf0248899
We generated a roGFP-CAAX construct (for mammalian expression) that can be used to examine the redox-state on the plasma membrane. Dihydroceramide desaturase regulates the compartmentalization of Rac1 for neuronal oxidative stress. Cell Rep. 33852856 FBrf0248757
A fluorogen activating protein neuropeptide (Dilp2-FAP) construct was used with membrane impermeant malachite green derivatives (MG-TCarb and MG-B-Tau) to detect neuropeptide release in the brain, specifically in LNv clock neurons Temporally and spatially partitioned neuropeptide release from individual clock neurons. Proc. Natl. Acad. Sci. U.S.A. 33875606 FBrf0248728
Here we design a microfluidic device capable of ensuring the normal development of multiple fly embryos as well as achieving real-time temperature control and fast temperature switches for quantitative live imaging with a home-built two-photon microscope. Quantifying Temperature Compensation of Bicoid Gradients with a Fast T-Tunable Microfluidic Device. Biophys. J. 32853562 FBrf0248966
We use whole-genome sequencing of Drosophila tissues (gut, head) to discover somatic genetic variation: 1- short-read Illumina sequencing of low-input DNA isolated from spontaneous clonal gut neoplasia, 2- long-read Oxford Nanopore (ONT) sequencing of DNA from pooled tissues. Unraveling the features of somatic transposition in the Drosophila intestine. EMBO J. 33634906 FBrf0248816
The work uses the isotropic fractionator method with Drosophila and mosquito brains. This method allows counting the number of cells in a tissue. If can be used with an antibody or genetic labeling (GAL4/UAS or QF/QUAS) and be applied to counting sub-populations of a tissue. The number of neurons in Drosophila and mosquito brains. PLoS ONE 33989293 FBrf0248958
GRAF plays a role in restricting the constriction of the actomyosin based contractile ring in cellularization. Spatiotemporal recruitment of RhoGTPase protein GRAF inhibits actomyosin ring constriction in Drosophila cellularization. eLife 33835025 FBrf0248856

Apr 2021

Author description of technical advance Title Journal PubMed ID FBrf number
We have developed an automated imaging system constituted of a light sheet fluorescence microscope on a chip that allows analysis of Drosophila embryos in suspension that are fluxing in through a microfluidic chamber. Automatic imaging of Drosophila embryos with light sheet fluorescence microscopy on chip. J. Biophotonics 33295053 FBrf0248287
Method to quantify epithelial barrier permeability in Drosophila imaginal discs using fluorescent dextran. The permeability of the experimental sample is compared to control samples that have a disrupted or non-functional barrier. Modified from Lamb et al. (1998). Ecdysone regulates the Drosophila imaginal disc epithelial barrier, determining the length of regeneration checkpoint delay. Development 33658221 FBrf0248455
We developed PEGASUS_flies, which calculates whole gene significance scores from variant P-values that were output in a GWAS. Our platform works well for Drosophila/Drosophila Genetic Reference Panel (DGRP) lines. Available at: https://github.com/ramachandran-lab/PEGASUS_flies Natural variation in the regulation of neurodevelopmental genes modifies flight performance in Drosophila. PLoS Genet. 33735180 FBrf0248437
Hypoxia chamber with strictly controlled environmental parameters Posthypoxic behavioral impairment and mortality of Drosophila melanogaster are associated with high temperatures, enhanced predeath activity and oxidative stress. Exp. Mol. Med. 33564101 FBrf0248297
We introduced DrosoX technique (Scitech Korea, Republic of Korea) for the quantitative analysis of food intake by individual flies. Cucurbitacin B Suppresses Hyperglycemia Associated with a High Sugar Diet and Promotes Sleep in Drosophila melanogaster. Mol. Cells 33542166 FBrf0248331
The "resource" is an accurate phylogeny for the montium group of Drosophila A phylogeny for the Drosophila montium species group: A model clade for comparative analyses. Molec. Phylog. Evol. 33387647 FBrf0248412
UAS-based transgenic lines for expressing genes from the SARS-CoV-2 virus that causes COVID-19 were generated. Functional analysis of SARS-CoV-2 proteins in Drosophila identifies Orf6-induced pathogenic effects with Selinexor as an effective treatment. Cell Biosci. 33766136 FBrf0248509
Targated DamID of olfactory sensory neuron populations Targeted molecular profiling of rare olfactory sensory neurons identifies fate, wiring, and functional determinants. eLife 33666172 FBrf0248540
pPWG-attB empty vector. A modified pPWG vector bearing the attB region inserted at a StuI site. It is compatible with Gateway system and can be used for random insertion in the genome (as a standard pPWG) but also in attB/P site specific integration ( phiC31 mediated). Mauve/LYST limits fusion of lysosome-related organelles and promotes centrosomal recruitment of microtubule nucleating proteins. Dev. Cell 33725482 FBrf0248552
Identification of mRNA targets of Ataxin2 (Atx2) in Drosophila brain by fusing it to the catalytic domain of adenosine deaminase (ADAR) enzyme. ADAR converts adenosine into inosine and subsequent RNA-Seq identifies these conversions (edits) as guanosines. Antagonistic roles for Ataxin-2 structured and disordered domains in RNP condensation. eLife 33689682 FBrf0248408
Single molecule fluorescence in situ hybridisation in whole Drosophila brain. Selective dendritic localization of mRNA in Drosophila mushroom body output neurons. eLife 33724180 FBrf0248505
Novel method to compare 3D chromatin conformation data in Drosophila Independence of chromatin conformation and gene regulation during Drosophila dorsoventral patterning. Nat. Genet. 33795866 FBrf0248615
A lineage recording system termed "intMEMOIR" designed for in situ readout, thereby enabling simultaneous analysis of cell lineage, state, and spatial organization in the same tissue. Imaging cell lineage with a synthetic digital recording system. Science 33833095 FBrf0248662

Mar 2021

Author description of technical advance Title Journal PubMed ID FBrf number
We describe a fluorescent in situ hybridization protocol for the detection of endogenous Drosophila gut microbiome bacteria in different sample types (isolated bacteria, feces, larval and adult guts). We also added an automated analysis pipeline, which should be useful for others. Visualization of endogenous gut bacteria in Drosophila melanogaster using fluorescence in situ hybridization. PLoS ONE 33606846 FBrf0248171
FreeClimber is an automated and high-throughput method for accurately and repeatably quantifying group climbing performance/climbing velocity/negative geotaxis in Drosophila. For more information, see the GitHub repository at: https://github.com/adamspierer/freeclimber FreeClimber: automated quantification of climbing performance in Drosophila. J. Exp. Biol. 33188065 FBrf0247781
CLADES, a tool to analyze neuronal lineages in Drosophila. A programmable sequence of reporters for lineage analysis. Nat. Neurosci. 32719561 FBrf0247972
The paper describes the use of Hedgehog signaling compenents: The signal Hedgehog and receptor Patched directed expression to model mutually exclusive computations in the context and highlights useful applications and tries to imagine the technology's potential. A Turing machine for the Life Sciences. D. I. S. FBrf0248044
New antibody, new transgenic lines, new S2 cell stable cell lines. Drosophila Tubulin-Specific Chaperone E Recruits Tubulin around Chromatin to Promote Mitotic Spindle Assembly. Curr. Biol. 33259793 FBrf0248211
In this manuscript it is reported a new setup to evaluate for the first time the release of neuroactive amines in Drosophila brain, by in vivo Fast-Scan Cyclic Voltammetry, while the fly is being exposed to odorants or an electric shock. Study of the release of endogenous amines in Drosophila brain in vivo in response to stimuli linked to aversive olfactory conditioning. J. Neurochem. 32596813 FBrf0248195
Generation of novel transgenic flies expressing a monocistronic version of the human FUS gene (expresses only the FUS protein or only the altFUS protein), as well as the wild-type human FUS gene (expresses both proteins, FUS and altFUS). The FUS gene is dual-coding with both proteins contributing to FUS-mediated toxicity. EMBO Rep. 33226175 FBrf0248130
Gene Drive element (split) located in specific Drosophila melanogaster genes. Inherently confinable split-drive systems in Drosophila. Nat. Commun. 33674604 FBrf0248266
By using the previously defined matrisomes of Drosophila, we analyzed recorded genotype-to-phenotype relationships to define the Drosophila extracellular matrix phenome. The extracellular matrix phenome across species. Matrix Biol Plus 33543035 FBrf0247970
This article indicates the maximum length of introgession segments that produce hybrid segmental offspring in heterozygosity, introgressing chromosomal segments of D. koepferae into a genetic background of D. buzzatii. Evaluation of Drosophila chromosomal segments proposed by means of simulations of possessing hybrid sterility genes from reproductive isolation. J. Genet. 33622987 FBrf0248240

Feb 2021

Author description of technical advance Title Journal PubMed ID FBrf number
This paper describes reagents (e.g. transgenic flies, plasmids, cloning protocols) to perform prime editing in Drosophila melanogaster. Precise genome engineering in Drosophila using prime editing. Proc. Natl. Acad. Sci. U.S.A. 33443210 FBrf0247772
Metabolic flux analysis of lipids. Lipidome-wide 13C flux analysis: a novel tool to estimate the turnover of lipids in organisms and cultures. J. Lipid Res. 31712250 FBrf0247854
Developmental scRNA-seq atlas of the Drosophila optic lobe. Neuronal diversity and convergence in a visual system developmental atlas. Nature 33149298 FBrf0247762
Application of digital droplet PCR in gene expression study. Genes regulating development and behavior exhibited altered expression in Drosophila melanogaster exposed to bisphenol A: use of real-time quantitative PCR (qRT-PCR) and droplet digital PCR (ddPCR) in genotoxicity study. Environ. Sci. Pollut. Res. Int. 33025430 FBrf0247932
The transgenic sexing strains of Drosophila suzukii based on the testis-specific fluorescent expression. Characterization of the Drosophila suzukii β2-tubulin gene and the utilization of its promoter to monitor sex separation and insemination. Gene 33346099 FBrf0247834
New model of flight exercise, new model of the Western Diet. Preference and detrimental effects of high fat, sugar, and salt diet in wild-caught Drosophila simulans are reversed by flight exercise. FASEB Bioadv 33490883 FBrf0247838
Identification of neutral lipid-based secreted structures called microcarriers in the lumen of the male accessory gland, which can be stained by neutral lipid dyes like LipidTox and Nile Red. Drosophila Sex Peptide controls the assembly of lipid microcarriers in seminal fluid. Proc. Natl. Acad. Sci. U.S.A. 33495334 FBrf0247869
Long-term in vivo imaging of Drosophila giant larvae tumor migration and invasion using SiMView microscopy. The level of oncogenic Ras determines the malignant transformation of Lkb1 mutant tissue in vivo. Commun. Biol. 33514834 FBrf0247944
Methods to examine the musculature of the Drosophila larva. These methods include analysis of the muscle sarcomeres, particularly in the same larva throughout the different larval instars. This work contains methods to muscle structural changes to muscle functional changes. Analyzing muscle structure and function throughout the larval instars in live Drosophila. STAR Protoc 33532738 FBrf0247996
We verified that Drosophila S2R+ adapted to grow in serum-free media is amenable to RNAi interference-mediated gene knockdown. Serum-free adapted Drosophila S2R+ line is amenable to RNA interference. Micropub Biol 33537561 FBrf0248021
Single cell genomics of testes. Dynamic sex chromosome expression in Drosophila male germ cells. Nat. Commun. 33563972 FBrf0248088
New reporter line and new null allele were generated in this paper. The Krüppel-like factor Cabut has cell cycle regulatory properties similar to E2F1. Proc. Natl. Acad. Sci. U.S.A. 33558234 FBrf0248123
Split-GAL4 lines labeling specific cell types. Neural circuit mechanisms of sexual receptivity in Drosophila females. Nature 33239786 FBrf0247919
A translational fidelity reporter (UAS-Fluc-STOP-Nluc) - Drosophila mutant strains (RPS23-R67K, RPS26-KO). Ribosomopathy-associated mutations cause proteotoxic stress that is alleviated by TOR inhibition. Nat. Cell Biol. 33495632 FBrf0248082
The modified PER assay can deliver stimuli not only for taste, but also for other senses. We made a line that can express the hair plate in legs. Multisensory interactions regulate feeding behavior in Drosophila. Proc. Natl. Acad. Sci. U.S.A. 33558226 FBrf0248109
UAS-MagIC, fluorescent Mg2+ reporter transgene. Magnesium efflux from Drosophila Kenyon cells is critical for normal and diet-enhanced long-term memory. eLife 33242000 FBrf0247921
Mathematical algorithm for cytoneme/Tumor microtube expansion. Modeling invasion patterns in the glioblastoma battlefield. PLoS Comput. Biol. 33513131 FBrf0248065
We developed a new technique called mosaic analysis by gRNA-induced crossing-over (MAGIC) for mosaic analysis with unmodified genomes. We developed the MAGIC toolkit for chromosomal arm 2L. Versatile CRISPR/Cas9-mediated mosaic analysis by gRNA-induced crossing-over for unmodified genomes. PLoS Biol. 33444322 FBrf0247818

Jan 2021

Author description of technical advance Title Journal PubMed ID FBrf number
Human genes expressed in breast cancer patients are screened for their ability to aberrate development of the Drosophila eye. Transgenic construct UAS-hRPS12 was described in this paper. HumanaFly: high-throughput transgenesis and expression of breast cancer transcripts in Drosophila eye discovers the RPS12-Wingless signaling axis. Sci. Rep. 33273532 FBrf0247452
Python-based code used to quantify object-to-object distances; e.g., mRNA to centrosomes. centrocortin RNA localization to centrosomes is regulated by FMRP and facilitates error-free mitosis. J. Cell Biol. 33196763 FBrf0247305
A single cell atlas of the proximal wing disc was built by single cell RNAseq. The myoblast, tracheal and epithelial cells associated with third instar larval wing disc were mapped. Diverse cell types along with specific markers were identified. A cell atlas of adult muscle precursors uncovers early events in fibre-type divergence in Drosophila. EMBO Rep. 32815271 FBrf0247435
Expansion microscopy for larval tissue. Recruitment of BAF to the nuclear envelope couples the LINC complex to endoreplication. Development 33168584 FBrf0247504
Several new fly lines. In particular: - a GFP-tagged FoxP gene - a null allele - a conditional UAS-gRNA-based knock-out line. Identification of FoxP circuits involved in locomotion and object fixation in Drosophila. Open Biol 33321059 FBrf0247550
Nuclear localization signal (NLS) that isolated from D. suzukii transformer gene. Bicistronic expression and differential localization of proteins in insect cells and Drosophila suzukii using picornaviral 2A peptides. Insect Biochem. Mol. Biol. 31978587 FBrf0245063
piggyBac constructs that express DeRed at embryonic stage. Identification and characterization of four Drosophila suzukii cellularization genes and their promoters. BMC Genet. 33339500 FBrf0247583
The protocol describes preparation of adult axenic Drosophila before monitoring their behavior in a two-choice feeding assay, where flies are confronted with an axenic versus a dead or alive bacteria-contaminated feeding solution. Protocol for a Binary Choice Feeding Assay Using Adult, Axenic Drosophila. STAR Protoc 33377013 FBrf0247622
CRISPR dual-gRNA transgenic targeting phosphoinositide signaling genes. A genome engineering resource to uncover principles of cellular organization and tissue architecture by lipid signaling. eLife 33320085 FBrf0247664
Tissue- and time-resolved chromatin accessibility during Drosophila embryogenesis. Lineage-Resolved Enhancer and Promoter Usage during a Time Course of Embryogenesis. Dev. Cell 33171098 FBrf0247494
We apply deep learning on thousands of mRNA datasets to examine the genetic regulatory code controlling mRNA abundance in model organisms including Drosophila melanogaster, and show that in all organisms mRNA abundance can be predicted directly from DNA sequence. Deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure. Nat. Commun. 33262328 FBrf0247517
UAS-driven regulatable fluorescent secretory cargo.] ESCargo: a regulatable fluorescent secretory cargo for diverse model organisms. Mol. Biol. Cell 33112725 FBrf0247546
1. S2 cell culture and luciferase reporter assay; 2. AGO1 immunoprecipitation (AGO1 IP); 3. Immunofluorescence experiments. Regulatory mechanism of daily sleep by miR-276a. FASEB J. 33337563 FBrf0247672
Resource: website for downloading aligned genome sequences from Drosophila pseudoobscura species group. PseudoBase: a genomic visualization and exploration resource for the Drosophila pseudoobscura subgroup. Fly 33319644 FBrf0247745
S2 cell culture and luciferase reporter assay; AGO1 immunoprecipitation. Regulation of circadian behavioural output via clock-responsive miR-276b. Insect Mol. Biol. 33131172 FBrf0247752
Superresolution imaging of glutamate receptors were obtained with structured illumination microscopy (SIM). Postsynaptic cAMP signalling regulates the antagonistic balance of Drosophila glutamate receptor subtypes. Development 33234716 FBrf0247665
Characterization of novel chromosomal structures in Drosophila embryonic cells, by combining 3D structured illumination microscopy (3D-SIM) and DAPI or FISH staining with a X Oligopaint probe (observation in a haploid context in sorted male embryos using a Y-GFP line). Ext. Fig.6. Regulation of single-cell genome organization into TADs and chromatin nanodomains. Nat. Genet. 33077913 FBrf0247675
The methods paper describes detailed procedure for X-ray fluorescence microscopy scanning of Drosophila oocytes and eggs to measure elemental distribution. Our report on the elemental distributions themselves was published in Hu et al. iScience 2020. X-ray fluorescence microscopy scanning of Drosophila oocytes and eggs. STAR Protoc 33437967 FBrf0247770

2020

Dec 2020

Author description of technical advance Title Journal PubMed ID FBrf number
Analysis of Gal4 expression patterns of commonly used Gal4 drivers in adult females. Analysis of Gal4 Expression Patterns in Adult Drosophila Females. G3 (Bethesda) 32917721 FBrf0247159
We defined the origins of repeat-derived RNAs and their specific chromatin locations in Drosophila S2 cells using the global RNA–DNA interaction sequencing method (GRID-seq). Active retrotransposons help maintain pericentromeric heterochromatin required for faithful cell division. Genome Res. 33060173 FBrf0247182
We have developed a novel automated Drosophila life cycle multi-phase transition (pupariation, eclosion, and death) timing detection and measurement system with high accuracy and high temporal resolution. The Drosophila Individual Activity Monitoring and Detection System (DIAMonDS). eLife 33168136 FBrf0247192
A hydrogen peroxide probe was detected in vivo through a burnt fluorescent probe (TCFB, 2-Dicyanomethylene-3-cyano-4,5,5-trimethyl-2,5-dihydrofuran) (Sedgwick et al., 2017). Intramacrophage ROS Primes the Innate Immune System via JAK/STAT and Toll Activation. Cell Rep. 33176146 FBrf0247218
The binary expression of different pro-apoptotic genes using 2A peptides. Functional characterization of the Drosophila suzukii pro-apoptotic genes reaper, head involution defective and grim. Apoptosis 33113043 FBrf0247316
Improved pipeline for CRISPR mediated genome editing in Drosophila species. Generation of new vector to make donor plasmids for homology-directed repair. A pipeline for precise and efficient genome editing by sgRNA-Cas9 RNPs in Drosophila. Fly 33016195 FBrf0247326
We describe a novel high throughput mass spectrometry approach to identifying species and sex by their metabolites. We show it works invertebrates generally, and can accurately distinguish closely related Drosophila (e.g. melanogaster and simulans) with potential for mass scoring. The application of rapid evaporative ionization mass spectrometry in the analysis of Drosophila species-a potential new tool in entomology. Open Biol. 33234068 FBrf0247327
Here we introduce TEchim, a new software that extracts chimeric sequencing reads that span transposon-gene breakpoints. In addition, we introduce scHardyWeinberg, a new approach to quantify co-expression levels in high-throughput single-cell sequencing data. Transposon expression in the Drosophila brain is driven by neighboring genes and diversifies the neural transcriptome. Genome Res. 32973040 FBrf0247119
Single-cell RNA-sequencing dataset of the adult Drosophila ovary containing transcriptome profiles for all major ovarian cell types. A single-cell atlas and lineage analysis of the adult Drosophila ovary. Nat. Commun. 33159074 FBrf0247148
We developed an optimized version of the bright and fast-maturing fluorescent protein mNeonGreen to serve as a real-time, quantitative reporter of gene/enhancer expression. A sensitive mNeonGreen reporter system to measure transcriptional dynamics in Drosophila development. Commun. Biol. 33184447 FBrf0247254
DRB treatment followed by Pol II ChIP. Evidence of slightly increased Pol II pausing in UPF1-depleted Drosophila melanogaster cells. Micropub Biol 33274326 FBrf0247413

Nov 2020

Author description of technical advance Title Journal PubMed ID FBrf number
Antibody. AANAT1 functions in astrocytes to regulate sleep homeostasis. eLife 32955431 FBrf0246918
Endogenous locus was edited with a two-step CRISPR/Cas9-mediated replacement. Humanization of Drosophila Gαo to Model GNAO1 Paediatric Encephalopathies. Biomedicines 33036271 FBrf0246897
We optimized, tested, and introduced a new method of automated count of Drosophila adults using the SeedCounter mobile application. The application is available on all mobile devices based on the Android system, and it does not require any additional equipment. Quantifying Drosophila adults with the use of a smartphone. Biol. Open 32917765 FBrf0246907
We introduce a developmental 96-well plate assay to use individual Drosophila larvae as tool for metabolic studies. How to use the development of individual Drosophila larvae as a metabolic sensor. J. Insect Physiol. 32783958 FBrf0246919
Novel method to compare 3D chromatin conformation data in Drosophila. CHESS enables quantitative comparison of chromatin contact data and automatic feature extraction. Nat. Genet. 33077914 FBrf0247073
Comprehensive calcium imaging from all 2,000 Kenyon cells in the mushroom body at single cell resolution. Synthesis of Conserved Odor Object Representations in a Random, Divergent-Convergent Network. Neuron 32814018 FBrf0247109
Dominant negative form of IP3R protein. It has three mutated amino acids which prevent ligand binding. IP3R being tetramer, requires IP3 binding to all monomers. Hence presence of even single IP3R-DN monomer in tetramer can render whole IP3R protein complex functionless. Modulation of flight and feeding behaviours requires presynaptic IP3Rs in dopaminergic neurons. eLife 33155978 FBrf0247160
Use of Hydrogel for live-imaging of Drosophila ovaries. Collective Cell Sorting Requires Contractile Cortical Waves in Germline Cells. Curr. Biol. 32916115 FBrf0247169
This paper uses fast-scan cyclic voltammetry at a carbon-fiber microelectrode to make real-time measurement of stimulated endogenous dopamine release in the mushroom body of adult Drosophila brains using various stimulation techniques. Real-Time Measurement of Stimulated Dopamine Release in Compartments of the Adult Drosophila melanogaster Mushroom Body. Anal. Chem. 33048531 FBrf0247175
New measurements of Position weight Matrices (PWMs) Dinucleotide Position weight Matrices (DPWMs) for 13 Drosophila transcription factors and their DNA shape analysis for all shape features. Transcription Factor Binding Affinities and DNA Shape Readout. iScience 33163946 FBrf0247184
Sequence, features, and schematic of the pWattB-nlacZ reporter construct vector. Three distinct mechanisms, Notch instructive, permissive, and independent, regulate the expression of two different pericardial genes to specify cardiac cell subtypes. PLoS ONE. 33108408 FBrf0247019
A new method for immobilizing explanted Drosophila tissue in agarose for use in long-term live imaging. An Immobilization Technique for Long-Term Time-Lapse Imaging of Explanted Drosophila Tissues. Front. Cell Dev. Biol. 33117817 FBrf0247101
Using new fast-scan cyclic voltammetry serotonin specific waveforms for in vivo detection of serotonin in Drosophila tissue. Improving serotonin fast-scan cyclic voltammetry detection: new waveforms to reduce electrode fouling. Analyst 32955048 FBrf0247149
We have developed a new protocol to indcue cell cycle arrest in early embryos, and deposited RNA-seq data for WT embryos and embryos arrested in cycle 12 for differernt amount of time. Interphase-arrested Drosophila embryos activate zygotic gene expression and initiate mid-blastula transition events at a low nuclear-cytoplasmic ratio. PLoS Biol. 33090988 FBrf0247179
Analysis of the chronometabolome including lipids. Loss of function in the Drosophila clock gene period results in altered intermediary lipid metabolism and increased susceptibility to starvation. Cell. Molec. Life Sci. 31960114 FBrf0247228
Transgenic Targeted DamID construct for the gene polycomb-like (Pcl) under the control of a UAS. Persistent epigenetic reprogramming of sweet taste by diet. Sci. Adv. 33177090 FBrf0247230

Oct 2020

Author description of technical advance Title Journal PubMed ID FBrf number
Small molecules called "HACs" alter normal autoprocessing activity of hedgehog precursor protein. Instead of reacting with cholesterol (cholesterolysis), the HACs alter hedgehog precursor autoprocessing toward a side reaction with water (hydrolysis). Subverting Hedgehog Protein Autoprocessing by Chemical Induction of Paracatalysis. Biochemistry 32013401 FBrf0246799
This paper shows how computational network analyses based on protein-protein interactions can be used to augment genetic screens to identify genes involved in essential developmental processes. The code are deposited in GitHub https://github.com/extavourlab/hpo_ova_eggL_screen. Topology-driven protein-protein interaction network analysis detects genetic sub-networks regulating reproductive capacity. eLife 32901612 FBrf0246922
PhotoGal4 is a phytochrome B-based optogenetic switch for fine tuned spatiotemporal control of gene expression in Drosophila explants. PhotoGal4 activates and deactivates gene expression upon red- or far-red-light irradiation. PhotoGal4: A Versatile Light-Dependent Switch for Spatiotemporal Control of Gene Expression in Drosophila Explants. iScience 32652492 FBrf0246250
We developed a unique visual stimulation setup to probe spectral, spatial, & temporal properties using neural activity imaging. Custom optical filters enabled simultaneous two-photon imaging & visual stimulation over a wide range of hues without compromising the temporal rates. A novel setup for simultaneous two-photon functional imaging and precise spectral and spatial visual stimulation in Drosophila. Sci. Rep. 32973185 FBrf0246808
New white gene mutant strains were generated in Drosophila suzukii and can be used as resources to study the corresponding phenotype. CRISPR/Cas9 mediated disruption of the white gene leads to pigmentation deficiency and copulation failure in Drosophila suzukii. J. Insect Physiol. 32745561 FBrf0246889
This protocol allows generation of homozygous mutant cell lines using an insertion cassette which autocatalytically generates insertion mutations in all alleles. Knockout cells generated using this method can be directly identified by PCR without a need for DNA sequencing. CRISPR-based engineering of gene knockout cells by homology-directed insertion in polyploid Drosophila S2R+ cells. Nat. Protoc. 32958931 FBrf0246845
Drosophila melanogaster line infected only with galbut virus (FoCo-17 line 30). Partitiviruses Infecting Drosophila melanogaster and Aedes aegypti Exhibit Efficient Biparental Vertical Transmission. J. Virol. 32759315 FBrf0246864
The isobaric tags for relative and absolute quantification (iTRAQ) technology was chosen to sequence the proteomes of Drosophila. Comparative proteomics analysis of dietary restriction in Drosophila. PLoS ONE 33064752 FBrf0246967