The microtubule plus end tracking protein orbit/MAST/CLASP acts downstream of the tyrosine kinase Abl in mediating axon guidance

被引:137
作者
Lee, H
Engel, U
Rusch, J
Scherrer, S
Sheard, K
Van Vactor, D
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol,Harvard Canc Ctr, Program Neurosci,Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med,Harvard Ctr Neurodegenerat & Repair, Dept Cell Biol, Program Neurosci, Boston, MA 02115 USA
关键词
D O I
10.1016/j.neuron.2004.05.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Axon guidance requires coordinated remodeling of actin and microtubule polymers. Using a genetic screen, we identified the microtubule-associated protein Orbit/MAST as a partner of the Abelson (Abl) tyrosine kinase. We find identical axon guidance phenotypes in orbit/MAST and Ab/ mutants at the midline, where the repellent Slit restricts axon crossing. Genetic interaction and epistasis assays indicate that Orbit/MAST mediates the action of Slit and its receptors, acting downstream of Abl. We find that Orbit/MAST protein localizes to Drosophila growth cones. Higher-resolution imaging of the Orbit/MAST ortholog CLASP in Xenopus growth cones suggests that this family of microtubule plus end tracking proteins identifies a subset of microtubules that probe the actin-rich peripheral growth cone domain, where guidance signals exert their initial influence on cytoskeletal organization. These and other data suggest a model where Abl acts as a central signaling node to coordinate actin and microtubule dynamics downstream of guidance receptors.
引用
收藏
页码:913 / 926
页数:14
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