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首页> 外文期刊>Molecular cell >Dom34: Hbs1 Plays a General Role in Quality-Control Systems by Dissociation of a Stalled Ribosome at the 3' End of Aberrant mRNA
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Dom34: Hbs1 Plays a General Role in Quality-Control Systems by Dissociation of a Stalled Ribosome at the 3' End of Aberrant mRNA

机译:Dom34:Hbs1通过异常mRNA的3'端失速的核糖体的解离在质量控制系统中发挥一般作用

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摘要

Translation arrest leads to an endonucleolytic cleavage of mRNA that is termed no-go decay (NGD). It has been reported that the Dom34:Hbs1 complex stimulates this endonucleolytic cleavage of mRNA induced by translation arrest in vivo and dissociates subunits of a stalled ribosome in vitro. Here we report that Dom34:Hbs1 dissociates the subunits of a ribosome that is stalled at the 3' end of mRNA in vivo, and has a crucial role in both NGD and nonstop decay. Dom34:Hbs1-mediated dissociation of a ribosome that is stalled at the 3' end of mRNA is required for degradation of a 5'-NGD intermediate. Dom34:Hbs1 facilitates the decay of nonstop mRNAs from the 3' end by exosomes and is required for the complete degradation of nonstop mRNA decay intermediates. We propose that Dom34:Hbs1 stimulates degradation of the 5'-NGD intermediate and of nonstop mRNA by dissociating the ribosome that is stalled at the 3' end of the mRNA.
机译:翻译停滞导致mRNA的内切核酸酶裂解,称为无衰变(NGD)。据报道,Dom34:Hbs1复合物在体内刺激由翻译停滞诱导的mRNA的这种内切核酸酶切割,并在体外解离停滞的核糖体的亚基。在这里我们报告说,Dom34:Hbs1解离了停滞在体内mRNA的3'端的核糖体的亚基,并且在NGD和不间断衰变中都具有至关重要的作用。 Dom34:Hbs1介导的核糖体停滞在mRNA 3'端的解离是降解5'-NGD中间体所必需的。 Dom34:Hbs1促进外泌体从3'末端开始不间断mRNA的降解,并且是不间断mRNA降解中间体完全降解所必需的。我们建议Dom34:Hbs1通过解离停滞在mRNA 3'末端的核糖体来刺激5'-NGD中间体和不间断mRNA的降解。

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