TNF-α诱导代谢紊乱中选择性剪接的rna -蛋白相互作用的全局分析

IF 3 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY FEBS Letters Pub Date : 2021-02-01 Epub Date: 2021-01-24 DOI:10.1002/1873-3468.14029
Jiss Maria Louis, Arjun Agarwal, Raviprasad Aduri, Indrani Talukdar
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引用次数: 6

摘要

在本报告中,我们利用RNA结合蛋白特异性数据库(RBPDB)和我们之前发表的RNA-seq数据,分析了RNA和RNA结合蛋白之间的相互作用,以破译选择性剪接在TNF-α诱导的代谢紊乱中的作用。我们鉴定了13395种独特的RNA- rbp相互作用,包括385种独特的RNA基序和35种rbp,其中一些(包括MBNL-1和3、ZFP36、ZRANB2和SNRPA)受TNF-α的转录调节。除了一些先前报道的rbp,如RBMX和HuR/ELAVL1,我们发现一些新的rbp,如ZRANB2和SNRPA,参与代谢综合征相关基因的调控,这些基因含有丰富的四聚体RNA序列(AUUU)。综上所述,这项研究为基于rna -蛋白相互作用的新型代谢综合征治疗方法铺平了道路。
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Global analysis of RNA-protein interactions in TNF-α induced alternative splicing in metabolic disorders.

In this report, using the database of RNA-binding protein specificities (RBPDB) and our previously published RNA-seq data, we analyzed the interactions between RNA and RNA-binding proteins to decipher the role of alternative splicing in metabolic disorders induced by TNF-α. We identified 13 395 unique RNA-RBP interactions, including 385 unique RNA motifs and 35 RBPs, some of which (including MBNL-1 and 3, ZFP36, ZRANB2, and SNRPA) are transcriptionally regulated by TNF-α. In addition to some previously reported RBPs, such as RBMX and HuR/ELAVL1, we found a few novel RBPs, such as ZRANB2 and SNRPA, to be involved in the regulation of metabolic syndrome-associated genes that contain an enrichment of tetrameric RNA sequences (AUUU). Taken together, this study paves the way for novel RNA-protein interaction-based therapeutics for treating metabolic syndromes.

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来源期刊
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
6.60
自引率
2.90%
发文量
303
审稿时长
1 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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