The Caenorhabditis elegans P21-activated kinases are differentially required for UNC-6/netrin-mediated commissural motor axon guidance

被引:48
|
作者
Lucanic, Mark
Kiley, Maureen
Ashcroft, Neville
L'Etoile, Noelle
Cheng, Hwai-Jong [1 ]
机构
[1] Univ Calif Davis, Ctr Neurosci, Davis, CA 95616 USA
[2] Univ Calif Davis, Cell & Dev Biol Grad Grp, Davis, CA 95616 USA
[3] Univ Calif Davis, Coll Biol Sci, Sect Neurobiol Physiol & Behav, Davis, CA 95616 USA
[4] Univ Calif Davis, Sch Med, Dept Pathol & Lab Med, Davis, CA 95616 USA
[5] Univ Sussex, Genome Damage & Stabil Ctr, Brighton BN1 9RR, E Sussex, England
[6] Univ Calif Davis, Dept Psychiat & Behav Sci, Sacramento, CA 95817 USA
来源
DEVELOPMENT | 2006年 / 133卷 / 22期
关键词
axon guidance; netrin; unc-73; rac; P21-activated kinase;
D O I
10.1242/dev.02648
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
P21 activated kinases (PAKs) are major downstream effectors of rac-related small GTPases that regulate various cellular processes. We have identified the new PAK gene max-2 in a screen for mutants disrupted in UNC-6/netrin-mediated commissural axon guidance. There are three Caenorhabditis elegans PAKs. We find that each C. elegans PAK represents a distinct group previously identified in other species. Here we examine their roles in the postembryonic migration of the P cell neuroblasts and the axon guidance of the ventral cord commissural motoneurons (VCCMNs). We find that the two PAKs, max-2 and pak-1, are redundantly required for P cell migration and function with UNC-73/Trio and the rac GTPases (CED-10 and MIG-2). During axon guidance of the VCCMNs, PAK-1 also acts with the rac GTPases, CED-10 and MIG-2, and is completely redundant with MAX-2. Interestingly, we find that unlike MAX-2 activity during P cell migration, for motoneuron axon guidance max-2 is also required in parallel to this PAK-1 pathway, independent of rac GTPase signaling. Finally, we provide evidence that MAX-2 functions downstream of the UNC-6/netrin receptor UNC-5 during axon repulsion and is an integral part of its signaling.
引用
收藏
页码:4549 / 4559
页数:11
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