The implications of structured 5′ untranslated regions on translation and disease

被引:266
作者
Pickering, BM
Willis, AE
机构
[1] Southampton Gen Hosp, CRC Wessex Med Oncol Unit, Southampton SO16 6YD, Hants, England
[2] Univ Leicester, Dept Biochem, Leicester LE1 7RH, Leics, England
基金
英国生物技术与生命科学研究理事会;
关键词
internal ribosome entry; 5 ' untranslated region; IRES; translation;
D O I
10.1016/j.semcdb.2004.11.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Translational control is a key step in eukaryotic gene expression. The majority of translational control occurs at the level of initiation, thus implicating the 5' untranslated region as a major site of translational regulation. Many growth-related mRNAs have atypical 5' UTRs, which are often long and GC-rich. Such features promote formation of stable secondary structure, and many mRNAs encoding proteins involved in cell growth, proliferation and apoptosis have structured 5' UTRs, which in many cases harbour internal ribosome entry sites (IRESs) and upstream open-reading frames (uORFs). In this review we discuss how secondary structural elements in the 5' UTR can regulate translation and how mutations that perturb these secondary structural elements can have implications for disease and tumourigenesis. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:39 / 47
页数:9
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