ARK-1 inhibits EGFR signaling in C-elegans

被引:84
作者
Hopper, NA
Lee, JH
Sternberg, PW
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[2] CALTECH, Howard Hughes Med Inst, Div Biol, Pasadena, CA 91125 USA
关键词
D O I
10.1016/S1097-2765(00)00008-3
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
A screen for synthetic enhancers of sli-1 identified ark-1 (for Ack-related tyrosine kinase), a novel inhibitor of let-23 EGFR signaling in C. elegans. An ark-l mutation synergizes with mutations in other negative regulators of let-23, resulting in increased RAS signaling. Genetic analysis suggests that ARK-1 acts upstream of RAS and is dependent upon SEM-5. ARK-1 inhibits LET-23-mediated ovulation, a RAS-independent function. ARK-1 physically interacts with SEM-5 in the yeast two-hybrid assay. We find that sem-5 also has a negative function in let-23-mediated ovulation and suggest that this negative function is mediated by the recruitment of inhibitors such as ARK-1.
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页码:65 / 75
页数:11
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