Distinct human NUMB isoforms regulate differentiation vs. proliferation in the neuronal lineage

被引:161
作者
Verdi, JM
Bashirullah, A
Goldhawk, DE
Kubu, CJ
Jamali, M
Meakin, SO
Lipshitz, HD
机构
[1] John P Robarts Res Inst, London, ON N6A 5K8, Canada
[2] Univ Western Ontario, Dept Physiol, London, ON, Canada
[3] Univ Western Ontario, Dept Biochem, London, ON, Canada
[4] Hosp Sick Children, Program Dev Biol, Inst Res, Toronto, ON M5G 1X8, Canada
[5] CALTECH, Div Biol, Pasadena, CA 91125 USA
[6] Univ Toronto, Dept Mol & Med Genet, Toronto, ON M5G 1X8, Canada
关键词
D O I
10.1073/pnas.96.18.10472
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neuronal cell fate decisions are directed in Drosophila by NUMB, a signaling adapter protein with two protein-protein interaction domains: a phosphotyrosine-binding domain and a proline-rich region (PRR) that functions as an SH3-binding domain, Here we show that there are at least four human NUMB isoforms and that these serve two distinct developmental functions in the neuronal lineage: differentiation (but not proliferation) is promoted by human NUMB protein isoforms with a type I (short) PRR. In contrast, proliferation (but not differentiation) is directed by isoforms that have a type II (long) PRR, The two types of PRR may promote distinct intracellular signaling pathways downstream of the NOTCH receptor during mammalian neurogenesis.
引用
收藏
页码:10472 / 10476
页数:5
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