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切割与聚腺苷酸化:终止信使RNA扩展基因调控。

Cleavage and polyadenylation: Ending the message expands gene regulation.

作者信息

Neve Jonathan, Patel Radhika, Wang Zhiqiao, Louey Alastair, Furger André Martin

机构信息

a Department of Biochemistry , University of Oxford , Oxford , United Kingdom.

出版信息

RNA Biol. 2017 Jul 3;14(7):865-890. doi: 10.1080/15476286.2017.1306171. Epub 2017 Apr 28.

Abstract

Cleavage and polyadenylation (pA) is a fundamental step that is required for the maturation of primary protein encoding transcripts into functional mRNAs that can be exported from the nucleus and translated in the cytoplasm. 3'end processing is dependent on the assembly of a multiprotein processing complex on the pA signals that reside in the pre-mRNAs. Most eukaryotic genes have multiple pA signals, resulting in alternative cleavage and polyadenylation (APA), a widespread phenomenon that is important to establish cell state and cell type specific transcriptomes. Here, we review how pA sites are recognized and comprehensively summarize how APA is regulated and creates mRNA isoform profiles that are characteristic for cell types, tissues, cellular states and disease.

摘要

切割与聚腺苷酸化(pA)是一个基本步骤,它是初级蛋白质编码转录本成熟为功能性mRNA所必需的,这些功能性mRNA能够从细胞核输出并在细胞质中进行翻译。3'端加工依赖于多蛋白加工复合体在位于前体mRNA中的pA信号上的组装。大多数真核基因具有多个pA信号,导致可变切割与聚腺苷酸化(APA),这是一种广泛存在的现象,对于建立细胞状态和细胞类型特异性转录组很重要。在这里,我们综述了pA位点是如何被识别的,并全面总结了APA是如何被调控的,以及如何产生对于细胞类型、组织、细胞状态和疾病具有特征性的mRNA异构体谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48cd/5546720/5e700426eac2/krnb-14-07-1306171-g001.jpg

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