Dendritic BC1 RNA in translational control mechanisms

被引:112
作者
Wang, HD
Iacoangeli, A
Lin, D
Williams, K
Denman, RB
Hellen, CUT
Tiedge, H [1 ]
机构
[1] SUNY Hlth Sci Ctr, Dept Physiol & Pharmacol, Brooklyn, NY 11203 USA
[2] SUNY Hlth Sci Ctr, Mol & Cellular Biol Program, Brooklyn, NY 11203 USA
[3] SUNY Hlth Sci Ctr, Dept Microbiol & Immunol, Brooklyn, NY 11203 USA
[4] SUNY Hlth Sci Ctr, Dept Neurol, Brooklyn, NY 11203 USA
[5] New York State Inst Basic Res Dev Disabil, Dept Mol Biol, Staten Isl, NY 10314 USA
关键词
D O I
10.1083/jcb.200506006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Translational control at the synapse is thought to be a key determinant of neuronal plasticity. How is such control implemented ? We report that small untranslated BC1 RNA is a specific effector of translational control both in vitro and in vivo. BC1 RNA, expressed in neurons and germ cells, inhibits a rate-limiting step in the assembly of translation initiation complexes. A translational repression element is contained within the unique 3' domain of BC1 RNA. Interactions of this domain with eukaryotic initiation factor 4A and poly( A) binding protein mediate repression, indicating that the 3' BC1 domain targets a functional interaction between these factors. In contrast, interactions of BC1 RNA with the fragile X mental retardation protein could not be documented. Thus, BC1 RNA modulates translation-dependent processes in neurons and germs cells by directly interacting with translation initiation factors.
引用
收藏
页码:811 / 821
页数:11
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