Opposing Feedbacks on Ras Tune Receptor Tyrosine Kinase Signaling

被引:2
|
作者
Perry, Michael [1 ]
Desplan, Claude [1 ,2 ]
机构
[1] NYU, Ctr Dev Genet, New York, NY 10003 USA
[2] NYU Abu Dhabi, Ctr Genom & Syst Biol, Abu Dhabi, U Arab Emirates
关键词
EGF RECEPTOR; INTEGRATION; PATHWAYS; CELL;
D O I
10.1126/scisignal.2004808
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Signaling in development is not always on or off; often, distinct intensity and duration of signaling leads to distinct outcomes. This is true for receptor tyrosine kinase (RTK) signaling in many contexts, where negative feedback often plays a role. Although such negative feedback might reduce or even turn off signaling output over time, continued signaling is often maintained for proper cell fate specification. In this issue, Sieglitz et al. identify a positive regulator of Ras-mediated RTK signaling that they name Rau. Rau is necessary to achieve specific signaling intensity for the differentiation of photoreceptors and of glia that wrap axons in the developing Drosophila eye disc. Both the negative regulator Sprouty and Rau influence signaling through the guanosine triphosphatase Ras; specifically, Rau forms a positive feedback loop important for counteracting the Sprouty negative feedback loop.
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页数:2
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