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顶复门寄生虫内的mRNA 3'端加工,经典参与者与意外参与者的拼凑组合。

3'-end mRNA processing within apicomplexan parasites, a patchwork of classic, and unexpected players.

作者信息

Swale Christopher, Hakimi Mohamed-Ali

机构信息

Team Host-Pathogen Interactions and Immunity to Infection, Institute for Advanced Biosciences, INSERM U1209, CNRS UMR5309, Grenoble Alpes University, Grenoble, France.

出版信息

Wiley Interdiscip Rev RNA. 2023 Sep-Oct;14(5):e1783. doi: 10.1002/wrna.1783. Epub 2023 Mar 30.

DOI:10.1002/wrna.1783
PMID:36994829
Abstract

The 3'-end processing of mRNA is a co-transcriptional process that leads to the formation of a poly-adenosine tail on the mRNA and directly controls termination of the RNA polymerase II juggernaut. This process involves a megadalton complex composed of cleavage and polyadenylation specificity factors (CPSFs) that are able to recognize cis-sequence elements on nascent mRNA to then carry out cleavage and polyadenylation reactions. Recent structural and biochemical studies have defined the roles played by different subunits of the complex and provided a comprehensive mechanistic understanding of this machinery in yeast or metazoans. More recently, the discovery of small molecule inhibitors of CPSF function in Apicomplexa has stimulated interest in studying the specificities of this ancient eukaryotic machinery in these organisms. Although its function is conserved in Apicomplexa, the CPSF complex integrates a novel reader of the N6-methyladenosine (m6A). This feature, inherited from the plant kingdom, bridges m6A metabolism directly to 3'-end processing and by extension, to transcription termination. In this review, we will examine convergence and divergence of CPSF within the apicomplexan parasites and explore the potential of small molecule inhibition of this machinery within these organisms. This article is categorized under: RNA Processing > 3' End Processing RNA Processing > RNA Editing and Modification.

摘要

mRNA的3'端加工是一个共转录过程,该过程导致mRNA上形成多聚腺苷酸尾巴,并直接控制RNA聚合酶II的终止。这个过程涉及一个由切割和聚腺苷酸化特异性因子(CPSF)组成的兆道尔顿复合物,这些因子能够识别新生mRNA上的顺式序列元件,进而进行切割和聚腺苷酸化反应。最近的结构和生化研究已经明确了该复合物不同亚基所起的作用,并对酵母或后生动物中这一机制有了全面的机械理解。最近,在顶复门生物中发现了CPSF功能的小分子抑制剂,这激发了人们研究这种古老真核生物机制在这些生物体中的特异性的兴趣。尽管其功能在顶复门生物中是保守的,但CPSF复合物整合了一种新型的N6-甲基腺苷(m6A)识别蛋白。这一从植物界继承而来的特征,将m6A代谢直接与3'端加工联系起来,并进而与转录终止联系起来。在这篇综述中,我们将研究顶复门寄生虫中CPSF的趋同和差异,并探索小分子抑制这些生物体中这一机制的潜力。本文分类如下:RNA加工>3'端加工;RNA加工>RNA编辑与修饰。

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