共 73 条
Regulating axon branch stability: The role of p190 RhoGAP in repressing a retraction signaling pathway
被引:175
作者:

Billuart, P
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机构:
Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA

Winter, CG
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机构:
Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA

Maresh, A
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Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA

Zhao, XS
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机构:
Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA

Luo, LQ
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机构:
Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
机构:
[1] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
来源:
关键词:
D O I:
10.1016/S0092-8674(01)00522-0
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:
Mechanisms that regulate axon branch stability are largely unknown. Genome-wide analyses of Rho GTPase activating protein (RhoGAP) function in Drosophila using RNA interference identified p190 RhoGAP as essential for axon stability in mushroom body neurons, the olfactory learning and memory center. p190 inactivation leads to axon branch retraction, a phenotype mimicked by activation of GTPase RhoA and its effector kinase Drok and modulated by the level and phosphorylation of myosin regulatory light chain. Thus, there exists a retraction pathway from RhoA to myosin in maturing neurons, which is normally repressed by p190. Local regulation of p190 could control the structural plasticity of neurons. Indeed, genetic evidence supports negative regulation of p190 by integrin and Src, both implicated in neural plasticity.
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页码:195 / 207
页数:13
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