The RNA-binding protein Musashi-1 regulates neural development through the translational repression of p21WAF-1

被引:144
作者
Battelli, C
Nikopoulos, GN
Mitchell, JG
Verdì, JM
机构
[1] Maine Med Ctr, Res Inst, Ctr Regenerat Med, Scarborough, ME 04074 USA
[2] Univ Sacred Heart, Dept Med Oncol, I-00168 Rome, Italy
[3] Univ Maine, Interdisciplinary Program Biochem & Mol Biol, Orono, ME 04469 USA
关键词
D O I
10.1016/j.mcn.2005.09.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
RNA-binding proteins regulate cell fate decisions during nervous system development. The Msi family of RNA-binding proteins is expressed in multipotential neural progenitors, and is required for maintaining cells in a proliferative state. We demonstrate that Msi-1's ability to regulate progenitor maintenance is through the translational inhibition of the cyclin-dependent kinase inhibitor p21(WAF-1). Msi-1 ectopic expression increases the proliferation rate and the capacity to regulate p21(WAF-1) protein expression, independent of p53. The 3' untranslated region (UTR) of the native p21(WAF-1) mRNA contains a Msi-1 consensus-binding site that permits Msi-1 to directly repress the translation of p21(WAF-1) protein. Reduction of Msi-1 through antisense leads to aberrant p21(WAF-1) expression, which significantly impairs neural differentiation. A double knockdown for p21(WAF-1) and Msi-1 rescues the production of mature MAP(+) neurons. Our results further elucidate the symbiotic relationship between cell cycle withdrawal and the onset of differentiation in the developing nervous system, as well as increasing the understanding of the influence that RNA-binding proteins serve in regulating these processes. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:85 / 96
页数:12
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