Synthetic lethal and convergent biological effects of cancer-associated spliceosomal gene mutations Journal Article


Authors: Lee, S. C. W.; North, K.; Kim, E.; Jang, E.; Obeng, E.; Lu, S. X.; Liu, B.; Inoue, D.; Yoshimi, A.; Ki, M.; Yeo, M.; Zhang, X. J.; Kim, M. K.; Cho, H.; Chung, Y. R.; Taylor, J.; Durham, B. H.; Kim, Y. J.; Pastore, A.; Monette, S.; Palacino, J.; Seiler, M.; Buonamici, S.; Smith, P. G.; Ebert, B. L.; Bradley, R. K.; Abdel-Wahab, O.
Article Title: Synthetic lethal and convergent biological effects of cancer-associated spliceosomal gene mutations
Abstract: Mutations affecting RNA splicing factors are the most common genetic alterations in myelodysplastic syndrome (MDS) patients and occur in a mutually exclusive manner. The basis for the mutual exclusivity of these mutations and how they contribute to MDS is not well understood. Here we report that although different spliceosome gene mutations impart distinct effects on splicing, they are negatively selected for when co-expressed due to aberrant splicing and downregulation of regulators of hematopoietic stem cell survival and quiescence. In addition to this synthetic lethal interaction, mutations in the splicing factors SF3B1 and SRSF2 share convergent effects on aberrant splicing of mRNAs that promote nuclear factor κB signaling. These data identify shared consequences of splicing-factor mutations and the basis for their mutual exclusivity. Lee et al. report that SF3B1 and SRSF2 mutations elicit distinct effects on splicing and are synthetically lethal due to the cumulative impact on hematopoietic stem cell survival and quiescence. These mutations share convergent effects on promoting NF-κB signaling to drive myelodysplastic syndrome. © 2018 Elsevier Inc.
Keywords: myelodysplastic syndromes; splicing; nf-κb; sf3b1; srsf2; u2af1
Journal Title: Cancer Cell
Volume: 34
Issue: 2
ISSN: 1535-6108
Publisher: Cell Press  
Date Published: 2018-08-13
Start Page: 225
End Page: 241.e8
Language: English
DOI: 10.1016/j.ccell.2018.07.003
PROVIDER: scopus
PUBMED: 30107174
PMCID: PMC6373472
DOI/URL:
Notes: Article -- Export Date: 4 September 2018 -- Source: Scopus
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