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mRNA 的多聚腺苷酸化和核输出。

Polyadenylation and nuclear export of mRNAs.

机构信息

From the MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge CB2 0QH, United Kingdom

出版信息

J Biol Chem. 2019 Mar 1;294(9):2977-2987. doi: 10.1074/jbc.REV118.005594. Epub 2019 Jan 25.

Abstract

In eukaryotes, the separation of translation from transcription by the nuclear envelope enables mRNA modifications such as capping, splicing, and polyadenylation. These modifications are mediated by a spectrum of ribonuclear proteins that associate with preRNA transcripts, coordinating the different steps and coupling them to nuclear export, ensuring that only mature transcripts reach the cytoplasmic translation machinery. Although the components of this machinery have been identified and considerable functional insight has been achieved, a number of questions remain outstanding about mRNA nuclear export and how it is integrated into the nuclear phase of the gene expression pathway. Nuclear export factors mediate mRNA transit through nuclear pores to the cytoplasm, after which these factors are removed from the mRNA, preventing transcripts from returning to the nucleus. However, as outlined in this review, several aspects of the mechanism by which transport factor binding and release are mediated remain unclear, as are the roles of accessory nuclear components in these processes. Moreover, the mechanisms by which completion of mRNA splicing and polyadenylation are recognized, together with how they are coordinated with nuclear export, also remain only partially characterized. One attractive hypothesis is that dissociating poly(A) polymerase from the cleavage and polyadenylation machinery could signal completion of mRNA maturation and thereby provide a mechanism for initiating nuclear export. The impressive array of genetic, molecular, cellular, and structural data that has been generated about these systems now provides many of the tools needed to define the precise mechanisms involved in these processes and how they are integrated.

摘要

在真核生物中,核膜将翻译与转录分隔开,从而使 mRNA 发生修饰,如加帽、剪接和多聚腺苷酸化。这些修饰由一系列核糖核蛋白介导,它们与前 RNA 转录本结合,协调不同步骤并将其与核输出偶联,以确保只有成熟的转录本到达细胞质翻译机制。尽管已经鉴定出该机制的组成部分,并获得了相当多的功能见解,但关于 mRNA 核输出及其如何与基因表达途径的核相整合仍存在一些悬而未决的问题。核输出因子介导 mRNA 通过核孔向细胞质转运,然后这些因子从 mRNA 上脱离,防止转录本返回细胞核。然而,正如本文综述所概述的,运输因子结合和释放介导机制的几个方面仍不清楚,辅助核成分在这些过程中的作用也不清楚。此外,mRNA 剪接和多聚腺苷酸化完成的识别机制以及它们如何与核输出协调也只是部分表征。一个有吸引力的假设是,从切割和多聚腺苷酸化机制中分离出多聚(A)聚合酶可以指示 mRNA 成熟的完成,从而为启动核输出提供一种机制。关于这些系统的大量遗传、分子、细胞和结构数据,现在为定义这些过程中涉及的精确机制以及它们如何整合提供了许多所需的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7bf/6398137/dc52e8bbb564/zbc0121902690001.jpg

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