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可变剪接和多聚腺苷酸化:程度、调控和功能。

Alternative cleavage and polyadenylation: extent, regulation and function.

机构信息

Division of Gene Regulation, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.

出版信息

Nat Rev Genet. 2013 Jul;14(7):496-506. doi: 10.1038/nrg3482.

Abstract

The 3' end of most protein-coding genes and long non-coding RNAs is cleaved and polyadenylated. Recent discoveries have revealed that a large proportion of these genes contains more than one polyadenylation site. Therefore, alternative polyadenylation (APA) is a widespread phenomenon, generating mRNAs with alternative 3' ends. APA contributes to the complexity of the transcriptome by generating isoforms that differ either in their coding sequence or in their 3' untranslated regions (UTRs), thereby potentially regulating the function, stability, localization and translation efficiency of target RNAs. Here, we review our current understanding of the polyadenylation process and the latest progress in the identification of APA events, mechanisms that regulate poly(A) site selection, and biological processes and diseases resulting from APA.

摘要

大多数蛋白质编码基因和长非编码 RNA 的 3' 端被切割和多聚腺苷酸化。最近的发现揭示了这些基因中的很大一部分含有不止一个多聚腺苷酸化位点。因此,选择性多聚腺苷酸化(APA)是一种广泛存在的现象,产生具有不同 3' 末端的 mRNA。APA 通过产生在其编码序列或 3' 非翻译区(UTR)中存在差异的异构体来增加转录组的复杂性,从而可能调节靶 RNA 的功能、稳定性、定位和翻译效率。在这里,我们回顾了我们对多聚腺苷酸化过程的理解以及 APA 事件、调节多聚(A)位点选择的机制、以及 APA 导致的生物学过程和疾病的最新进展。

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