Analysis of Gal4 Expression Patterns in Adult Drosophila Females

Abstract Precise genetic manipulation of specific cell types or tissues to pinpoint gene function requirement is a critical step in studies aimed at unraveling the intricacies of organismal physiology. Drosophila researchers heavily rely on the UAS/Gal4/Gal80 system for tissue-specific manipulations...

Full description

Saved in:
Bibliographic Details
Published inG3 : genes - genomes - genetics Vol. 10; no. 11; pp. 4147 - 4158
Main Authors Weaver, Lesley N, Ma, Tianlu, Drummond-Barbosa, Daniela
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.11.2020
Genetics Society of America
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Abstract Precise genetic manipulation of specific cell types or tissues to pinpoint gene function requirement is a critical step in studies aimed at unraveling the intricacies of organismal physiology. Drosophila researchers heavily rely on the UAS/Gal4/Gal80 system for tissue-specific manipulations; however, it is often unclear whether the reported Gal4 expression patterns are indeed specific to the tissue of interest such that experimental results are not confounded by secondary sites of Gal4 expression. Here, we surveyed the expression patterns of commonly used Gal4 drivers in adult Drosophila female tissues under optimal conditions and found that multiple drivers have unreported secondary sites of expression beyond their published cell type/tissue expression pattern. These results underscore the importance of thoroughly characterizing Gal4 tools as part of a rigorous experimental design that avoids potential misinterpretation of results as we strive for understanding how the function of a specific gene/pathway in one tissue contributes to whole-body physiology.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Present address: Department of Biology, Indiana University, Bloomington, IN 47405.
ISSN:2160-1836
2160-1836
DOI:10.1534/g3.120.401676