Upf1, an RNA helicase required for nonsense-mediated mRNA decay, modulates the transcriptional response to oxidative stress in fission yeast

被引:60
|
作者
Rodriguez-Gabriel, Miguel A.
Watt, Stephen
Bahler, Jurg
Russell, Paul
机构
[1] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[3] Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England
[4] Univ Complutense Madrid, Fac Farm, Dept Microbiol 2, E-28040 Madrid, Spain
基金
英国惠康基金;
关键词
D O I
10.1128/MCB.00286-06
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
In the fission yeast Schizosaccharomyces pombe, oxidative stress triggers the activation of the Spc1/Sty1 mitogen-activated protein kinase, which in turn phosphorylates the Atf1/Pcr1 heterodimeric transcription factor to effect global changes in the patterns of gene expression. This transcriptional response is also controlled by Csx1, an RNA-binding protein that directly associates with and stabilizes atf1(+) mRNA. Here we report the surprising observation that this response also requires Upf1, a component of the nonsense-mediated mRNA decay (NMD) system. Accordingly, upfl Delta and csx1 Delta strains are similarly sensitive to oxidative stress, and the effects of the mutations are not additive, suggesting that Upft and Csx1 work in the same pathway to stabilize atf1(+) mRNA during oxidative stress. Consistent with these observations, wholle-genome expression profiling studies have shown that Upf1 controls the expression of more than 100 genes that are transcriptionally induced in response to oxidative stress, the large majority of which are also controlled by AM and Csx1. The unexpected connection between an NMD factor and the oxidative stress response in fission yeast may provide important new clues about the physiological function of NMD in other species.
引用
收藏
页码:6347 / 6356
页数:10
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