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哺乳动物进化过程中启动子和增强子的重编程。

Repurposing of promoters and enhancers during mammalian evolution.

机构信息

Center for Integrative Genomics, University of Lausanne, CH-1015, Lausanne, Switzerland.

Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge, CB2 1QN, United Kingdom.

出版信息

Nat Commun. 2018 Oct 4;9(1):4066. doi: 10.1038/s41467-018-06544-z.

Abstract

Promoters and enhancers-key controllers of gene expression-have long been distinguished from each other based on their function. However, recent work suggested that common architectural and functional features might have facilitated the conversion of one type of element into the other during evolution. Here, based on cross-mammalian analyses of epigenome and transcriptome data, we provide support for this hypothesis by detecting 445 regulatory elements with signatures of activity turnover (termed P/E elements). Most events represent transformations of putative ancestral enhancers into promoters, leading to the emergence of species-specific transcribed loci or 5' exons. Distinct GC sequence compositions and stabilizing 5' splicing (U1) regulatory motif patterns may have predisposed P/E elements to regulatory repurposing, and changes in the U1 and polyadenylation signal densities and distributions likely drove the evolutionary activity switches. Our work suggests that regulatory repurposing facilitated regulatory innovation and the origination of new genes and exons during evolution.

摘要

启动子和增强子——基因表达的主要控制器——长期以来一直根据其功能区分开来。然而,最近的研究表明,在进化过程中,共同的结构和功能特征可能促进了一种元件类型向另一种元件类型的转化。在这里,我们基于跨哺乳动物的表观基因组和转录组数据分析,通过检测 445 个具有活性转换特征的调控元件(称为 P/E 元件),为这一假说提供了支持。大多数事件代表假定的祖先增强子向启动子的转化,导致物种特异性转录基因座或 5' 外显子的出现。不同的 GC 序列组成和稳定的 5' 剪接(U1)调控模体模式可能使 P/E 元件易于进行调控再利用,而 U1 和多聚腺苷酸化信号密度和分布的变化可能驱动了进化活性开关。我们的工作表明,在进化过程中,调控再利用促进了调控创新和新基因和外显子的起源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0bd/6172195/d7924ca6ced4/41467_2018_6544_Fig1_HTML.jpg

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