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非编码 RNA 基因的可变剪接调控。

Alternative splicing modulation by G-quadruplexes.

机构信息

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.

Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, CA, 94158, USA.

出版信息

Nat Commun. 2022 May 3;13(1):2404. doi: 10.1038/s41467-022-30071-7.

Abstract

Alternative splicing is central to metazoan gene regulation, but the regulatory mechanisms are incompletely understood. Here, we show that G-quadruplex (G4) motifs are enriched ~3-fold near splice junctions. The importance of G4s in RNA is emphasised by a higher enrichment for the non-template strand. RNA-seq data from mouse and human neurons reveals an enrichment of G4s at exons that were skipped following depolarisation induced by potassium chloride. We validate the formation of stable RNA G4s for three candidate splice sites by circular dichroism spectroscopy, UV-melting and fluorescence measurements. Moreover, we find that sQTLs are enriched at G4s, and a minigene experiment provides further support for their role in promoting exon inclusion. Analysis of >1,800 high-throughput experiments reveals multiple RNA binding proteins associated with G4s. Finally, exploration of G4 motifs across eleven species shows strong enrichment at splice sites in mammals and birds, suggesting an evolutionary conserved splice regulatory mechanism.

摘要

可变剪接是真核生物基因调控的核心,但调控机制尚不完全清楚。在这里,我们表明 G-四联体(G4)基序在剪接接头附近富集约 3 倍。G4 在 RNA 中的重要性通过非模板链的更高富集得到强调。来自小鼠和人类神经元的 RNA-seq 数据显示,在钾离子诱导去极化后跳过的外显子中 G4 富集。我们通过圆二色性光谱、UV 熔融和荧光测量验证了三个候选剪接位点的稳定 RNA G4 的形成。此外,我们发现 sQTL 在 G4 处富集,并且迷你基因实验为它们在促进外显子包含中的作用提供了进一步的支持。对 >1800 个高通量实验的分析揭示了与 G4 相关的多种 RNA 结合蛋白。最后,对 11 个物种的 G4 基序的探索表明,在哺乳动物和鸟类中剪接位点有很强的富集,这表明存在进化保守的剪接调控机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3c6/9065059/8ce8fb6d694f/41467_2022_30071_Fig1_HTML.jpg

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