A GAL4-Driver Line Resource for Drosophila Neurobiology

Arnim Jenett(Howard Hughes Medical Institute), Gerald M. Rubin(Howard Hughes Medical Institute), Teri-T B Ngo(Howard Hughes Medical Institute), David Shepherd(Bangor University), Christine Murphy(Howard Hughes Medical Institute), Heather Dionne(Howard Hughes Medical Institute), Barret D. Pfeiffer(Howard Hughes Medical Institute), Amanda Cavallaro(Howard Hughes Medical Institute), Donald Hall(Howard Hughes Medical Institute), Jennifer Jeter(Howard Hughes Medical Institute), Nirmala Iyer(Howard Hughes Medical Institute), Dona Fetter(Howard Hughes Medical Institute), Joanna H Hausenfluck(Howard Hughes Medical Institute), Hanchuan Peng(Howard Hughes Medical Institute), Eric T. Trautman(Howard Hughes Medical Institute), Robert Svirskas(Howard Hughes Medical Institute), Eugene W. Myers(Howard Hughes Medical Institute), Z. R. Iwiński(Carl Zeiss (United States)), Yoshinori Aso(Howard Hughes Medical Institute), Gina M DePasquale(Howard Hughes Medical Institute), Adrianne I. Enos(Howard Hughes Medical Institute), Phuson Hulamm(Howard Hughes Medical Institute), S. Lam(Howard Hughes Medical Institute), Hsing-Hsi Li(Howard Hughes Medical Institute), Todd Laverty(Howard Hughes Medical Institute), Fuhui Long(Howard Hughes Medical Institute), Lei Qu(Howard Hughes Medical Institute), Sean D. Murphy(Howard Hughes Medical Institute), Konrad Rokicki(Howard Hughes Medical Institute), Todd Safford(Howard Hughes Medical Institute), Kshiti Shaw(Howard Hughes Medical Institute), J. Simpson(Howard Hughes Medical Institute), Allison Sowell(Howard Hughes Medical Institute), Susana Tae(Howard Hughes Medical Institute), Yang Yu(Howard Hughes Medical Institute), Christopher T Zugates(Howard Hughes Medical Institute)
Cell Reports
October 1, 2012
Cited by 1,637Open Access
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Abstract

We established a collection of 7,000 transgenic lines of Drosophila melanogaster. Expression of GAL4 in each line is controlled by a different, defined fragment of genomic DNA that serves as a transcriptional enhancer. We used confocal microscopy of dissected nervous systems to determine the expression patterns driven by each fragment in the adult brain and ventral nerve cord. We present image data on 6,650 lines. Using both manual and machine-assisted annotation, we describe the expression patterns in the most useful lines. We illustrate the utility of these data for identifying novel neuronal cell types, revealing brain asymmetry, and describing the nature and extent of neuronal shape stereotypy. The GAL4 lines allow expression of exogenous genes in distinct, small subsets of the adult nervous system. The set of DNA fragments, each driving a documented expression pattern, will facilitate the generation of additional constructs for manipulating neuronal function.


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