PREMATURE TRANSLATIONAL TERMINATION TRIGGERS MESSENGER-RNA DECAPPING

被引:334
作者
MUHLRAD, D
PARKER, R
机构
[1] Department of Molecular and Cellular Biology, Life Sciences South, University of Arizona, Tucson
关键词
D O I
10.1038/370578a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
THE degradation of messenger RNA in eukaryotic cells is initiated by endonucleolytic cleavage(1,2) or by shortening of the poly(A) tail(3-6), which for some mRNAs activates a deadenylation-dependent decapping reaction(7). One type of rapid mRNA degradation in eukaryotes is caused by premature termination of translation(8,9). This turnover process prevents the translation of aberrant mRNAs(10,11), may affect the abundance and splicing pattern of nuclear transcripts(12,13), and may be involved in the aetiology of human genetic disease(14). Here we show that premature translational termination in yeast triggers decapping, independent of deadenylation, thereby exposing the transcript to 5'-to-3' degradation. Inactivation of the 5'-to-3' exonuclease reveals an additional 3'-to-5' pathway of mRNA turnover. These observations provide in vivo evidence for two new mechanisms of mRNA decay.
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页码:578 / 581
页数:4
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