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泛组织分析等位基因交替多聚腺苷酸化提示广泛的功能调节。

Pan-tissue analysis of allelic alternative polyadenylation suggests widespread functional regulation.

机构信息

Department of Biology, Southern University of Science and Technology, Shenzhen, China.

Laboratory of RNA Biochemistry, Institute of Chemistry and Biochemistry, Freie Universität Berlin, Berlin, Germany.

出版信息

Mol Syst Biol. 2020 Apr;16(4):e9367. doi: 10.15252/msb.20199367.

Abstract

Alternative polyadenylation (APA) is a major layer of gene regulation. However, it has recently been argued that most APA represents molecular noise. To clarify their functional relevance and evolution, we quantified allele-specific APA patterns in multiple tissues from an F1 hybrid mouse. We found a clearly negative correlation between gene expression and APA diversity for the 2,866 genes (24.9%) with a dominant polyadenylation site (PAS) usage above or equal to 90%, suggesting that their other PASs represent molecular errors. Among the remaining genes with multiple PASs, 3,971 genes (34.5%) express two or more isoforms with potentially functional importance. Interestingly, the genes with potentially functional minor PASs specific to neuronal tissues often express two APA isoforms with distinct subcellular localizations. Furthermore, our analysis of cis-APA divergence shows its pattern across tissues is distinct from that of gene expression. Finally, we demonstrate that the relative usage of alternative PASs is not only affected by their cis-regulatory elements, but also by potential coupling between transcriptional and APA regulation as well as competition kinetics between alternative sites.

摘要

可变多聚腺苷酸化(APA)是基因调控的主要层面之一。然而,最近有人认为,大多数 APA 代表分子噪声。为了阐明其功能相关性和进化,我们在 F1 杂交鼠的多种组织中定量了等位基因特异性 APA 模式。我们发现,在具有主导多聚腺苷酸化位点(PAS)使用频率高于或等于 90%的 2866 个基因(占 24.9%)中,基因表达与 APA 多样性之间存在明显的负相关,这表明它们的其他 PAS 代表分子错误。在具有多个 PAS 的剩余基因中,有 3971 个基因(占 34.5%)表达具有潜在功能重要性的两种或更多种异构体。有趣的是,具有特定于神经元组织的潜在功能次要 PAS 的基因通常表达两种具有不同亚细胞定位的 APA 异构体。此外,我们对顺式 APA 差异的分析表明,其在组织中的模式与基因表达的模式不同。最后,我们证明替代 PAS 的相对使用不仅受其顺式调控元件的影响,还受转录和 APA 调控之间的潜在耦合以及替代位点之间的竞争动力学的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f25b/7170663/1f7a5a5b0a3d/MSB-16-e9367-g003.jpg

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