Reprogramming the genetic code: The emerging role of ribosomal frameshifting in regulating cellular gene expression

被引:45
作者
Advani, Vivek M. [1 ]
Dinman, Jonathan D. [1 ]
机构
[1] Univ Maryland, Dept Cell Biol & Mol Genet, College Pk, MD 20742 USA
基金
美国国家卫生研究院;
关键词
cancer; frameshifting; miRNA; NMD; polyA track; pseudoknot; ribosome; ribosomopathy; SCA26; telomere; translation; MESSENGER-RNA SURVEILLANCE; TRANSLATIONAL FIDELITY; STIMULATION; PSEUDOURIDYLATION; RPL10; FRAME; YEAST; LEADS;
D O I
10.1002/bies.201500131
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Reading frame maintenance is a critical property of ribosomes. However, a number of genetic elements have been described that can induce ribosomes to shift on mRNAs, the most well understood of which are a class that directs ribosomal slippage by one base in 5' (-1) direction. This is referred to as programmed -1 ribosomal frame-shifting (-1 PRF). Recently, a new -1 PRF promoting element was serendipitously discovered in a study examining the effects of stretches of adenosines in the coding sequences of mRNAs. Here, we discuss this finding, recent studies describing how -1 PRF is used to control gene expression in eukaryotes, and how -1 PRF is itself regulated. The implications of dysregulation of -1 PRF on human health are examined, as are possible new areas in which novel -1 PRF promoting elements might be discovered.
引用
收藏
页码:21 / 26
页数:6
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