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首轮mRNA翻译的证据:在哺乳动物细胞中,受无义介导衰变作用的mRNA与CBP80和CBP20结合。

Evidence for a pioneer round of mRNA translation: mRNAs subject to nonsense-mediated decay in mammalian cells are bound by CBP80 and CBP20.

作者信息

Ishigaki Y, Li X, Serin G, Maquat L E

机构信息

Department of Biochemistry and Biophysics, School of Medicine and Dentistry, University of Rochester, 601 Elmwood Avenue, Box 712, Rochester, NY 14642, USA.

出版信息

Cell. 2001 Sep 7;106(5):607-17. doi: 10.1016/s0092-8674(01)00475-5.

Abstract

Nonsense-mediated decay (NMD) eliminates mRNAs that prematurely terminate translation. We used antibody to the nuclear cap binding protein CBP80 or its cytoplasmic counterpart eIF4E to immunopurify RNP containing nonsense-free or nonsense-containing transcripts. Data indicate that NMD takes place in association with CBP80. We defined other components of NMD-susceptible mRNP as CBP20, PABP2, eIF4G, and the NMD factors Upf2 and Upf3. Consistent with the dependence of NMD on translation, the NMD of CBP80-bound mRNA is blocked by cycloheximide or suppressor tRNA. These findings provide evidence that translation can take place in association with CBP80. They also indicate that CBP80-bound mRNA undergoes a "pioneer" round of translation, before CBP80-CBP20 are replaced by eIF4E, and Upf2 and Upf3 proteins dissociate from upstream of exon-exon junctions.

摘要

无义介导的mRNA降解(NMD)可消除过早终止翻译的mRNA。我们使用针对核帽结合蛋白CBP80或其细胞质对应物eIF4E的抗体,免疫纯化包含无义或含无义转录本的核糖核蛋白(RNP)。数据表明,NMD与CBP80相关联发生。我们将NMD敏感的mRNA核糖核蛋白的其他成分定义为CBP20、PABP2、eIF4G以及NMD因子Upf2和Upf3。与NMD对翻译的依赖性一致,环己酰亚胺或抑制性tRNA可阻断与CBP80结合的mRNA的NMD。这些发现提供了证据,表明翻译可与CBP80相关联进行。它们还表明,在CBP80-CBP20被eIF4E取代且Upf2和Upf3蛋白从外显子-外显子连接上游解离之前,与CBP80结合的mRNA会经历一轮“先驱”翻译。

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