Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

RNA-binding protein RBM20 represses splicing to orchestrate cardiac pre-mRNA processing

[img] PDF - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
2MB

Item Type:Article
Title:RNA-binding protein RBM20 represses splicing to orchestrate cardiac pre-mRNA processing
Creators Name:Maatz, H. and Jens, M. and Liss, M. and Schafer, S. and Heinig, M. and Kirchner, M. and Adami, E. and Rintisch, C. and Dauksaite, V. and Radke, M.H. and Selbach, M. and Barton, P.J.R. and Cook, S.A. and Rajewsky, N. and Gotthardt, M. and Landthaler, M. and Hubner, N.
Abstract:Mutations in the gene encoding the RNA-binding protein RBM20 have been implicated in dilated cardiomyopathy (DCM), a major cause of chronic heart failure, presumably through altering cardiac RNA splicing. Here, we combined transcriptome-wide crosslinking immunoprecipitation (CLIP-seq), RNA-seq, and quantitative proteomics in cell culture and rat and human hearts to examine how RBM20 regulates alternative splicing in the heart. Our analyses revealed the presence of a distinct RBM20 RNA-recognition element that is predominantly found within intronic binding sites and linked to repression of exon splicing with RBM20 binding near 3' and 5' splice sites. Proteomic analysis determined that RBM20 interacts with both U1 and U2 small nuclear ribonucleic particles (snRNPs) and suggested that RBM20-dependent splicing repression occurs through spliceosome stalling at complex A. Direct RBM20 targets included several genes previously shown to be involved in DCM as well as genes not typically associated with this disease. In failing human hearts, reduced expression of RBM20 affected alternative splicing of several direct targets, indicating that differences in RBM20 expression may affect cardiac function. Together, these findings identify RBM20-regulated targets and provide insight into the pathogenesis of human heart failure.
Keywords:Alternative Splicing, Base Sequence, Binding Sites, Cardiac Myocytes, Cohort Studies, Dilated Cardiomyopathy, Exons, Heart Failure, Mutation, Myocardium, Post-Transcriptional RNA Processing, RNA Precursors, RNA Splice Sites, RNA-Binding Proteins, Sprague-Dawley Rats, U1 Small Nuclear Ribonucleoprotein, U2 Small Nuclear Ribonucleoprotein, Genetic Selection, Spliceosomes, Animals, Rats
Source:Journal of Clinical Investigation
ISSN:0021-9738
Publisher:American Society for Clinical Investigation (U.S.A.)
Volume:124
Number:8
Page Range:3419-3430
Date:1 August 2014
Official Publication:https://doi.org/10.1172/JCI74523
PubMed:View item in PubMed

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library