Pak functions downstream of dock to regulate photoreceptor axon guidance in Drosophila

被引:245
作者
Hing, H
Xiao, J
Harden, N
Lim, L
Zipursky, SL [1 ]
机构
[1] Calif State Univ Los Angeles, Sch Med, Dept Biol Chem, Howard Hughes Med Inst, Los Angeles, CA 90095 USA
[2] Natl Univ Singapore, Inst Mol & Cell Biol, Singapore 117548, Singapore
[3] Inst Neurol, London WC1N 1PJ, England
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0092-8674(00)80798-9
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
The SH2/SH3 adaptor protein Dock has been proposed to transduce signals from guidance receptors to the actin cytoskeleton in Drosophila photoreceptor (R cell) growth cones. Here, we demonstrate that Drosophila p21-activated kinase (Pak) is required in a Dock pathway regulating R cell axon guidance and targeting. Dock and Pak colocalize to R cell axons and growth cones, physically interact, and their loss-of-function phenotypes are indistinguishable. Normal patterns of R cell connectivity require Pak's kinase activity and binding sites for both Dock and Cdc42/Rac. A membrane-tethered form of Pak (Pak(myr)) acts as a dominant gain-of-function protein. Retinal expression of Pak(myr) rescues the R cell connectivity phenotype in dock mutants. These data establish Pak as a critical regulator of axon guidance and a downstream effector of Dock in vivo.
引用
收藏
页码:853 / 863
页数:11
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