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Published on: May 7, 2018
The master switch gene sex-lethal promotes female development by negatively regulating the N-signaling pathway
1Department of Molecular Biology, Princeton University, Princeton, NJ 08540, USA.
Abstract:
Notch (N) signaling is used for cell-fate determination in many different developmental contexts. Here, we show that the master control gene for sex determination in Drosophila melanogaster, Sex-lethal (Sxl), negatively regulates the N-signaling pathway in females. In genetic assays, reducing Sxl activity suppresses the phenotypic effects of N mutations, while increasing Sxl activity enhances the effects. Sxl appears to negatively regulate the pathway by reducing N protein accumulation, and higher levels of N are found in Sxl(-) clones than in adjacent wild-type cells. The inhibition of N expression does not depend on the known downstream targets of Sxl; however, we find that Sxl protein can bind to N mRNAs. Finally, our results indicate that downregulation of the N pathway by Sxl contributes to sex-specific differences in morphology and suggest that it may also play an important role in follicle cell specification during oogenesis.
Insights
The Sex-lethal (Sxl) gene in female Drosophila melanogaster negatively regulates Notch (N) signaling. Sxl protein binds to N mRNAs, impacting cell fate and development.
Area of Science:
- Developmental biology
- Genetics
- Cell signaling
Background:
- Notch (N) signaling is crucial for cell-fate determination during development.
- The master control gene for sex determination in Drosophila melanogaster is Sex-lethal (Sxl).
Purpose of the Study:
- To investigate the regulatory relationship between Sex-lethal (Sxl) and Notch (N) signaling in Drosophila melanogaster.
- To determine how Sxl influences N signaling in female development.
Main Methods:
- Genetic assays were performed to assess the effects of altered Sxl activity on N signaling.
- Protein accumulation levels of N were measured in Sxl mutant clones.
- Sxl protein binding to N mRNAs was investigated.
Main Results:
- Sex-lethal (Sxl) negatively regulates the Notch (N) signaling pathway in female Drosophila.
- Reduced Sxl activity suppresses N mutation phenotypes, while increased Sxl activity enhances them.
- Sxl protein binds to N mRNAs, leading to reduced N protein accumulation.
Conclusions:
- Downregulation of the N pathway by Sxl contributes to sex-specific morphological differences.
- Sxl-mediated regulation of N signaling may be important for oogenesis and follicle cell specification.
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