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mRNA 质量控制进入调控阶段。

mRNP quality control goes regulatory.

机构信息

Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, CH-3012 Bern, Switzerland.

出版信息

Trends Genet. 2012 Feb;28(2):70-7. doi: 10.1016/j.tig.2011.11.001. Epub 2011 Dec 9.

Abstract

The accuracy of eukaryotic gene expression relies on efficient quality control (QC). Most steps in the gene expression pathway en route from transcription to translation are error-prone and QC systems have evolved to utilise many of these biochemical processes as checkpoints to monitor the production or function of mRNA-protein particles (mRNPs). Mechanistically, such evaluation of mRNP fitness is based on competition between the opposing activities of mRNP biogenesis and/or function and mRNP turnover. In fact, quite subtle alteration of any parameter can tip the balance between mRNP persistence and degradation and, therefore, QC checkpoints also comprise perfect opportunities for controlling cellular levels of individual or even entire families of transcripts. From this perspective, QC and gene regulation represent two outcomes of the same molecular process.

摘要

真核生物基因表达的准确性依赖于有效的质量控制 (QC)。从转录到翻译的基因表达途径中的大多数步骤都是易错的,QC 系统已经进化到利用许多这些生化过程作为检查点来监测 mRNA-蛋白颗粒 (mRNP) 的产生或功能。从机制上讲,这种 mRNP 适应性的评估基于 mRNP 生物发生和/或功能与 mRNP 周转率之间的相反活动的竞争。事实上,任何参数的细微改变都可能打破 mRNP 持久性和降解之间的平衡,因此,QC 检查点也是控制单个甚至整个转录本家族细胞水平的绝佳机会。从这个角度来看,QC 和基因调控代表了同一分子过程的两种结果。

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