Molecular impact of mutations in RNA splicing factors in cancer Review


Authors: Zhang, Q.; Ai, Y.; Abdel-Wahab, O.
Review Title: Molecular impact of mutations in RNA splicing factors in cancer
Abstract: Somatic mutations in genes encoding components of the RNA splicing machinery occur frequently in multiple forms of cancer. The most frequently mutated RNA splicing factors in cancer impact intronic branch site and 3' splice site recognition. These include mutations in the core RNA splicing factor SF3B1 as well as mutations in the U2AF1/2 heterodimeric complex, which recruits the SF3b complex to the 3' splice site. Additionally, mutations in splicing regulatory proteins SRSF2 and RBM10 are frequent in cancer, and there has been a recent suggestion that variant forms of small nuclear RNAs (snRNAs) may contribute to splicing dysregulation in cancer. Here, we describe molecular mechanisms by which mutations in these factors alter splice site recognition and how studies of this process have yielded new insights into cancer pathogenesis and the molecular regulation of splicing. We also discuss data linking mutant RNA splicing factors to RNA metabolism beyond splicing.
Keywords: genes; r-loop; expression; binding; sensitivity; landscape; site; myelodysplasia; srsf2 mutations; sf3b1 mutations
Journal Title: Molecular Cell
Volume: 84
Issue: 19
ISSN: 1097-2765
Publisher: Cell Press  
Date Published: 2024-10-03
Start Page: 3667
End Page: 3680
Language: English
ACCESSION: WOS:001331605400001
DOI: 10.1016/j.molcel.2024.07.019
PROVIDER: Clarivate Analytics Web of Science
PROVIDER: wos
PMCID: PMC11455611
PUBMED: 39146933
Notes: Review -- Source: Wos
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  1. Qian Zhang
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  2. Yuxi Ai
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