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组织特异性可变多聚腺苷酸化的机制:睾丸、脑及其他组织(2018 更新)。

Tissue-specific mechanisms of alternative polyadenylation: Testis, brain, and beyond (2018 update).

机构信息

Department of Cell Biology & Biochemistry, Texas Tech University Health Sciences Center, Lubbock, Texas.

出版信息

Wiley Interdiscip Rev RNA. 2019 Jul;10(4):e1526. doi: 10.1002/wrna.1526. Epub 2019 Feb 27.

Abstract

Alternative polyadenylation (APA) is how genes choose different sites for 3' end formation for mRNAs during transcription. APA often occurs in a tissue- or developmental stage-specific manner that can significantly affect gene activity by changing the protein product generated, the stability of the transcript, its localization within the cell, or its translatability. Despite the important regulatory effects that APA has on tissue-specific gene expression, only a few examples have been characterized mechanistically. In this 2018 update to our 2010 review, we examine mechanisms for the control of APA and update our understanding of the older mechanisms since 2010. We once postulated the existence of tissue-specific factors in APA. However, while a few tissue-specific polyadenylation factors are known, the emerging conclusion is that the majority of APA is accomplished by altering levels of core polyadenylation proteins. Examples of those core proteins include CSTF2, CPSF1, and subunits of mammalian cleavage factor I. But despite support for these mechanisms, no one has yet documented any of these proteins changing in either a tissue-specific or developmental manner. Given the profound effect that APA can have on gene expression and human health, improved understanding of tissue-specific APA could lead to numerous advances in gene activity control. This article is categorized under: RNA Processing > 3' End Processing RNA in Disease and Development > RNA in Development.

摘要

可变多聚腺苷酸化 (APA) 是指基因在转录过程中选择不同的 3' 末端形成位点的方式。APA 通常以组织或发育阶段特异性的方式发生,通过改变产生的蛋白质产物、转录本的稳定性、其在细胞内的定位或其翻译能力,显著影响基因活性。尽管 APA 对组织特异性基因表达具有重要的调节作用,但只有少数例子从机制上进行了描述。在 2010 年综述的基础上,我们在 2018 年的更新中检查了 APA 控制的机制,并更新了自 2010 年以来对旧机制的理解。我们曾经假设 APA 中存在组织特异性因子。然而,尽管已经知道了一些组织特异性多聚腺苷酸化因子,但新兴的结论是,大多数 APA 是通过改变核心多聚腺苷酸化蛋白的水平来完成的。这些核心蛋白的例子包括 CSTF2、CPSF1 和哺乳动物切割因子 I 的亚基。但是,尽管这些机制得到了支持,但没有人记录到这些蛋白质中的任何一种以组织特异性或发育方式发生变化。鉴于 APA 对基因表达和人类健康可能产生的深远影响,对组织特异性 APA 的深入了解可能会导致基因活性控制方面的许多进展。本文归类于:RNA 加工 > 3' 末端加工 RNA 在疾病与发育中的作用 > RNA 在发育中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c90b/6617714/8ab8f82a18d5/WRNA-10-na-g001.jpg

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