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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.

Original publication

DOI

10.15252/embj.201489852

Type

Journal article

Journal

The EMBO journal

Publication Date

03/2015

Volume

34

Pages

653 - 668

Addresses

Department of Biochemistry, University of Cambridge, Cambridge, UK.

Keywords

Hela Cells, Humans, RNA-Binding Proteins, Polypyrimidine Tract-Binding Protein, Nuclear Matrix-Associated Proteins, RNA, Small Interfering, DNA Primers, Electrophoresis, Polyacrylamide Gel, Microarray Analysis, Gene Expression Profiling, Reverse Transcriptase Polymerase Chain Reaction, Computational Biology, RNA Interference, Alternative Splicing, Gene Regulatory Networks, HEK293 Cells