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Updated: May 24, 2026

Preparation of Developing and Adult Drosophila Brains and Retinae for Live Imaging
Published on: March 15, 2010
The role of the small GTPase Rap in Drosophila R7 photoreceptor specification
Yannis Emmanuel Mavromatakis1, Andrew Tomlinson
1Department of Genetics and Development, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
Abstract:
The Drosophila R7 photoreceptor provides an excellent model system with which to study how cells receive and "decode" signals that specify cell fate. R7 is specified by the combined actions of the receptor tyrosine kinase (RTK) and Notch (N) signaling pathways. These pathways interact in a complex manner that includes antagonistic effects on photoreceptor specification: RTK promotes the photoreceptor fate, whereas N inhibits. Although other photoreceptors are subject to only mild N activation, R7 experiences a high-level N signal. To counter this effect and to ensure that the cell is specified as a photoreceptor, a high RTK signal is transduced in the cell. Thus, there are two levels of RTK transduction in the photoreceptors: in R7 it is high, whereas in others it is low. Here, we address how this high-level RTK signal is transduced in R7 and find that, in addition to Ras, another small GTPase, Rap, is also engaged. Thus, when N activity is high, a robust RTK signal operates that uses both Ras and Rap, but when N activity is low, only a mild RTK signal is transduced and Ras alone suffices for the purpose.
Insights
The Drosophila R7 photoreceptor uses both Ras and Rap small GTPases for robust signaling when Notch (N) pathway activity is high. When N activity is low, only Ras is needed for mild receptor tyrosine kinase (RTK) signaling.
Area of Science:
- Cell biology
- Neuroscience
- Developmental biology
Background:
- The Drosophila R7 photoreceptor is a model for cell fate specification.
- Receptor tyrosine kinase (RTK) and Notch (N) signaling pathways interact antagonistically to specify cell fate.
- R7 photoreceptors require high RTK signaling to overcome strong N pathway inhibition.
Purpose of the Study:
- To investigate the mechanisms of high-level RTK signal transduction in Drosophila R7 photoreceptors.
- To understand how RTK signaling is modulated by the N pathway in cell fate determination.
Main Methods:
- Utilized Drosophila R7 photoreceptor as a model system.
- Investigated the roles of small GTPases, Ras and Rap, in RTK signal transduction.
- Analyzed the interplay between RTK and N signaling pathways.
Main Results:
- High RTK signal transduction in R7 photoreceptors involves both Ras and Rap small GTPases.
- When N pathway activity is high, a robust RTK signal engages both Ras and Rap.
- When N pathway activity is low, a mild RTK signal relies solely on Ras.
Conclusions:
- The R7 photoreceptor employs distinct RTK signaling mechanisms depending on N pathway activity levels.
- Both Ras and Rap GTPases are crucial for robust RTK signaling in R7 under high N conditions.
- Ras GTPase alone is sufficient for mild RTK signaling in R7 when N activity is low.
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