Near-cognate peptidyl-tRNAs promote+1 programmed translational frameshifting in yeast

被引:52
作者
Sundararajan, A
Michaud, WA
Qian, Q
Stahl, G
Farabaugh, PJ [1 ]
机构
[1] Univ Maryland Baltimore Cty, Dept Biol Sci, Baltimore, MD 21250 USA
[2] Univ Maryland Baltimore Cty, Program Mol & Cell Biol, Baltimore, MD 21250 USA
关键词
D O I
10.1016/S1097-2765(00)80229-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Translational frameshifting is a ubiquitous, if rare, form of alternative decoding in which ribosomes spontaneously shift reading frames during translation elongation. In studying +1 frameshifting in Ty retrotransposons of the yeast S. cerevisiae, we previously showed that unusual P site tRNAs induce frameshifting. The frameshift-inducing tRNAs we show here are near-cognates for the P site codon. Their abnormal decoding induces frameshifting in either of two ways: weak codon-anticodon pairing allows the tRNA to disengage from the mRNA and slip +1, or an unusual codon-anticodon structure interferes with cognate in-frame decoding allowing out-of-frame decoding in the A site. We draw parallels between this mechanism and a proposed mechanism of frameshift suppression by mutant tRNAs.
引用
收藏
页码:1005 / 1015
页数:11
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