| Literature DB >> 32234239 |
Qiankun Niu1, Wei Wang1, Zhe Wei1, Boseon Byeon1, Asim Bikas Das1, Bo-Shiun Chen2, Wei-Hua Wu3.
Abstract
The yeast ATP-dependent chromatin remodeling enzyme Fun30 has been shown to regulate heterochromatin silencing, DNA repair, transcription, and chromatin organization. Although chromatin structure has been proposed to influence splice site recognition and regulation, whether ATP-dependent chromatin remodeling enzyme plays a role in regulating splicing is not known. In this study, we find that pre-mRNA splicing efficiency is impaired and the recruitment of spliceosome is compromised in Fun30-depleted cells. In addition, Fun30 is enriched in the gene body of individual intron-containing genes. Moreover, we show that pre-mRNA splicing efficiency is dependent on the chromatin remodeling activity of Fun30. The function of Fun30 in splicing is further supported by the observation that, Smarcad1, the mammalian homolog of Fun30, regulates alternative splicing. Taken together, these results provide evidence for a novel role of Fun30 in regulating splicing. Published by Elsevier Inc.Entities:
Keywords: Alternative splicing; Chromatin remodeling; Fun30; Pre-mRNA splicing; Smarcad1
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Year: 2020 PMID: 32234239 PMCID: PMC7285982 DOI: 10.1016/j.bbrc.2020.02.175
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575