The divergent Robo family protein Rig-1/Robo3 is a negative regulator of slit responsiveness required for midline crossing by commissural axons

被引:323
作者
Sabatier, C
Plump, AS
Ma, L
Brose, K
Tamada, A
Murakami, F
Lee, EYHP
Tessier-Lavigne, M [1 ]
机构
[1] Stanford Univ, Howard Hughes Med Inst, Dept Sci Biol, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Anat, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[4] Natl Inst Basic Biol, Div Behav & Neurobiol, Okazaki, Aichi 4448585, Japan
[5] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92697 USA
[6] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92697 USA
[7] Genentech Inc, San Francisco, CA 94080 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0092-8674(04)00303-4
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
Commissural axons in vertebrates and insects are initially attracted to the nervous system midline, but once they reach this intermediate target they undergo a dramatic switch, becoming responsive to repellent Slit proteins at the midline, which expel them onto the next leg of their trajectory. We have unexpectedly implicated a divergent member of the Robo family, Rig-1 (or Robo3), in preventing premature Slit sensitivity in mammals. Expression of Rig-1 protein by commissural axons is inversely correlated with Slit sensitivity. Removal of Rig-1 results in a total failure of commissural axons to cross. Genetic and in vitro analyses indicate that Rig-1 functions to repress Slit responsiveness similarly to Commissureless (Comm) in Drosophila. Unlike Comm, however, Rig-1 does not produce its effect by downregulating Robo receptors on precrossing commissural axon membranes. These results identify a mechanism for regulating Slit repulsion that helps choreograph the precise switch from attraction to repulsion at a key intermediate axonal target.
引用
收藏
页码:157 / 169
页数:13
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