Cancer-associated SF3B1 mutations affect alternative splicing by promoting alternative branchpoint usage
Mutations in the splicing factor SF3B1 are found in uveal melanoma. Here, Alsafadi et al. use RNA-sequencing data from these cancers and experimental models, and show that mutant SF3B1 promotes alternative branchpoints in a specific gene subset and that the mutant protein gains a new function.
Saved in:
Main Authors: | Samar Alsafadi, Alexandre Houy, Aude Battistella, Tatiana Popova, Michel Wassef, Emilie Henry, Franck Tirode, Angelos Constantinou, Sophie Piperno-Neumann, Sergio Roman-Roman, Martin Dutertre, Marc-Henri Stern |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2016
|
Subjects: | |
Online Access: | https://doaj.org/article/895eb1555d734fbe947b98b9284ba24c |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Alternative Splicing in Apicomplexan Parasites
by: Lee M. Yeoh, et al.
Published: (2019) -
Identification of prognostic alternative splicing events in sarcoma
by: Hongshuai Li, et al.
Published: (2021) -
An alternative splicing signature in human Crohn’s disease
by: Daowei Li, et al.
Published: (2021) -
Regulation of alternative splicing in obesity-induced hypertension
by: Dlamini Z, et al.
Published: (2019) -
Dysregulation of alternative splicing is associated with the pathogenesis of ulcerative colitis
by: Daowei Li, et al.
Published: (2021)