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An EP overexpression screen for genetic modifiers of Notch pathway function in Drosophila melanogaster

Published online by Cambridge University Press:  04 May 2004

LAUREN E. HALL
Affiliation:
Department of Biology, Emory University, Atlanta, GA, 30322, USA
SHAUNA J. ALEXANDER
Affiliation:
Department of Biology, Emory University, Atlanta, GA, 30322, USA
MICHAEL CHANG
Affiliation:
Department of Biology, Emory University, Atlanta, GA, 30322, USA
NATHANIEL S. WOODLING
Affiliation:
Department of Biology, Emory University, Atlanta, GA, 30322, USA
BARRY YEDVOBNICK
Affiliation:
Department of Biology, Emory University, Atlanta, GA, 30322, USA
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Abstract

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The Notch pathway comprises a signal transduction cascade required for the proper formation of multiple tissues during metazoan development. Originally described in Drosophila for its role in nervous system formation, the pathway has attracted much wider interest owing to its fundamental roles in a range of developmental and disease-related processes. Despite extensive analysis, Notch signaling is not completely understood and it appears that additional components of the pathway remain to be identified and characterized. Here, we describe a novel genetic strategy to screen for additional Notch pathway genes. The strategy combines partial loss of function for pathway activity with Enhancer-promoter (EP)-induced overexpression of random loci across the dorsoventral wing margin. Mastermind (Mam) is a nuclear component of the Notch signaling cascade. Using a GAL4-UAS-driven dominant-negative form of Mam, we created a genotype that exhibits a completely penetrant dominant wing-nicking phenotype. This phenotype was assayed for enhancement or suppression after outcrossing to several thousand EP lines. The screen identified known components or modifiers of Notch pathway function, as well as several potential new components. Our results suggest that a genetic screen that combines partial loss of function with random gene overexpression might be a useful strategy in the analysis of developmental pathways.

Type
Research Article
Copyright
© 2004 Cambridge University Press