RNA剪接
内含子
生物
遗传学
计算生物学
选择性拼接
第二组内含子
外显子
核糖核酸
基因
作者
Kazuhiro Fukumura,Luca Sperotto,Stefanie Seuß,Hyun-Seo Kang,Rei Yoshimoto,Michael Sattler,Akila Mayeda
出处
期刊:Cell Reports
[Cell Press]
日期:2023-12-01
卷期号:42 (12): 113534-113534
被引量:3
标识
DOI:10.1016/j.celrep.2023.113534
摘要
Human pre-mRNA splicing requires the removal of introns with highly variable lengths, from tens to over a million nucleotides. Therefore, mechanisms of intron recognition and splicing are likely not universal. Recently, we reported that splicing in a subset of human short introns with truncated polypyrimidine tracts depends on RBM17 (SPF45), instead of the canonical splicing factor U2 auxiliary factor (U2AF) heterodimer. Here, we demonstrate that SAP30BP, a factor previously implicated in transcriptional control, is an essential splicing cofactor for RBM17. In vitro binding and nuclear magnetic resonance analyses demonstrate that a U2AF-homology motif (UHM) in RBM17 binds directly to a newly identified UHM-ligand motif in SAP30BP. We show that this RBM17-SAP30BP interaction is required to specifically recruit RBM17 to phosphorylated SF3B1 (SF3b155), a U2 small nuclear ribonucleoprotein (U2 snRNP) component in active spliceosomes. We propose a mechanism for splicing in a subset of short introns, in which SAP30BP guides RBM17 in the assembly of active spliceosomes.
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