Hardy Jessica G, Norbury Chris J
Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, U.K.
Biochem Soc Trans. 2016 Aug 15;44(4):1051-7. doi: 10.1042/BST20160078.
Most mammalian protein coding genes are subject to alternative cleavage and polyadenylation (APA), which can generate distinct mRNA 3'UTRs with differing regulatory potential. Although this process has been intensely studied in recent years, it remains unclear how and to what extent cleavage site selection is regulated under different physiological conditions. The cleavage factor Im (CFIm) complex is a core component of the mammalian cleavage machinery, and the observation that its depletion causes transcriptome-wide changes in cleavage site use makes it a key candidate regulator of APA. This review aims to summarize current knowledge of the CFIm complex, and explores the evidence surrounding its potential contribution to regulation of APA.
大多数哺乳动物蛋白质编码基因会发生可变切割和多聚腺苷酸化(APA),这一过程可产生具有不同调控潜力的独特mRNA 3'UTR。尽管近年来对这一过程进行了深入研究,但仍不清楚在不同生理条件下切割位点的选择是如何以及在多大程度上受到调控的。切割因子Im(CFIm)复合物是哺乳动物切割机制的核心组成部分,其缺失会导致转录组范围内切割位点使用情况的变化,这一现象使其成为APA调控的关键候选调节因子。本综述旨在总结目前关于CFIm复合物的知识,并探讨其对APA调控潜在贡献的相关证据。