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Nuclear matrix protein Matrin3 regulates alternative splicing and forms overlapping regulatory networks with PTB.
- Source :
-
The EMBO journal [EMBO J] 2015 Mar 04; Vol. 34 (5), pp. 653-68. Date of Electronic Publication: 2015 Jan 19. - Publication Year :
- 2015
-
Abstract
- Matrin3 is an RNA- and DNA-binding nuclear matrix protein found to be associated with neural and muscular degenerative diseases. A number of possible functions of Matrin3 have been suggested, but no widespread role in RNA metabolism has yet been clearly demonstrated. We identified Matrin3 by its interaction with the second RRM domain of the splicing regulator PTB. Using a combination of RNAi knockdown, transcriptome profiling and iCLIP, we find that Matrin3 is a regulator of hundreds of alternative splicing events, principally acting as a splicing repressor with only a small proportion of targeted events being co-regulated by PTB. In contrast to other splicing regulators, Matrin3 binds to an extended region within repressed exons and flanking introns with no sharply defined peaks. The identification of this clear molecular function of Matrin3 should help to clarify the molecular pathology of ALS and other diseases caused by mutations of Matrin3.<br /> (© 2015 The Authors. Published under the terms of the CC BY 4.0 license.)
- Subjects :
- Alternative Splicing genetics
Computational Biology
DNA Primers genetics
Electrophoresis, Polyacrylamide Gel
Gene Expression Profiling
Gene Regulatory Networks genetics
HEK293 Cells
HeLa Cells
Humans
Microarray Analysis
RNA Interference
RNA, Small Interfering genetics
Reverse Transcriptase Polymerase Chain Reaction
Alternative Splicing physiology
Gene Regulatory Networks physiology
Nuclear Matrix-Associated Proteins metabolism
Polypyrimidine Tract-Binding Protein metabolism
RNA-Binding Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1460-2075
- Volume :
- 34
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- The EMBO journal
- Publication Type :
- Academic Journal
- Accession number :
- 25599992
- Full Text :
- https://doi.org/10.15252/embj.201489852