共 109 条
Mechanisms of translational control by the 3′ UTR in development and differentiation
被引:275
作者:

de Moor, CH
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机构:
Univ Nottingham, Sch Biomed Sci, Ctr Biochem & Cell Biol, Nottingham NG7 2UH, England Univ Nottingham, Sch Biomed Sci, Ctr Biochem & Cell Biol, Nottingham NG7 2UH, England

Meijer, H
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机构:
Univ Nottingham, Sch Biomed Sci, Ctr Biochem & Cell Biol, Nottingham NG7 2UH, England Univ Nottingham, Sch Biomed Sci, Ctr Biochem & Cell Biol, Nottingham NG7 2UH, England

Lissenden, S
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机构:
Univ Nottingham, Sch Biomed Sci, Ctr Biochem & Cell Biol, Nottingham NG7 2UH, England Univ Nottingham, Sch Biomed Sci, Ctr Biochem & Cell Biol, Nottingham NG7 2UH, England
机构:
[1] Univ Nottingham, Sch Biomed Sci, Ctr Biochem & Cell Biol, Nottingham NG7 2UH, England
基金:
英国惠康基金;
英国生物技术与生命科学研究理事会;
关键词:
3 ' UTR;
development and differentiation;
cell cycle;
gene expression;
translation;
D O I:
10.1016/j.semcdb.2004.11.007
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Translational control plays a major role in early development, differentiation and the cell cycle. In this review, we focus on the four main mechanisms of translational control by 3' untranslated regions: 1. Cytoplasmic polyadenylation and deadenylation; 2. Recruitment of 4E binding proteins; 3 Regulation of ribosomal subunit binding; 4. Post-initiation repression by microRNAs. Proteins with conserved functions in translational control during development include cytoplasmic polyadenylation element binding proteins (CPEB/Orb), Pumilio, Bruno, Fragile X mental retardation protein and RNA helicases. The translational regulation of the mRNAs encoding cyclin B1, Oskar, Nanos, Male specific lethal 2 (Msl-2), lipoxygenase and Lin-14 is discussed. (C) 2004 Elsevier Ltd. All rights reserved.
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页码:49 / 58
页数:10
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