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Muscle-Specific Mis-Splicing and Heart Disease Exemplified by RBM20

Alternative splicing is an essential post-transcriptional process to generate multiple functional RNAs or proteins from a single transcript. Progress in RNA biology has led to a better understanding of muscle-specific RNA splicing in heart disease. The recent discovery of the muscle-specific splicin...

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Autores principales: Rexiati, Maimaiti, Sun, Mingming, Guo, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793171/
https://www.ncbi.nlm.nih.gov/pubmed/29304022
http://dx.doi.org/10.3390/genes9010018
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author Rexiati, Maimaiti
Sun, Mingming
Guo, Wei
author_facet Rexiati, Maimaiti
Sun, Mingming
Guo, Wei
author_sort Rexiati, Maimaiti
collection PubMed
description Alternative splicing is an essential post-transcriptional process to generate multiple functional RNAs or proteins from a single transcript. Progress in RNA biology has led to a better understanding of muscle-specific RNA splicing in heart disease. The recent discovery of the muscle-specific splicing factor RNA-binding motif 20 (RBM20) not only provided great insights into the general alternative splicing mechanism but also demonstrated molecular mechanism of how this splicing factor is associated with dilated cardiomyopathy. Here, we review our current knowledge of muscle-specific splicing factors and heart disease, with an emphasis on RBM20 and its targets, RBM20-dependent alternative splicing mechanism, RBM20 disease origin in induced Pluripotent Stem Cells (iPSCs), and RBM20 mutations in dilated cardiomyopathy. In the end, we will discuss the multifunctional role of RBM20 and manipulation of RBM20 as a potential therapeutic target for heart disease.
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spelling pubmed-57931712018-02-07 Muscle-Specific Mis-Splicing and Heart Disease Exemplified by RBM20 Rexiati, Maimaiti Sun, Mingming Guo, Wei Genes (Basel) Review Alternative splicing is an essential post-transcriptional process to generate multiple functional RNAs or proteins from a single transcript. Progress in RNA biology has led to a better understanding of muscle-specific RNA splicing in heart disease. The recent discovery of the muscle-specific splicing factor RNA-binding motif 20 (RBM20) not only provided great insights into the general alternative splicing mechanism but also demonstrated molecular mechanism of how this splicing factor is associated with dilated cardiomyopathy. Here, we review our current knowledge of muscle-specific splicing factors and heart disease, with an emphasis on RBM20 and its targets, RBM20-dependent alternative splicing mechanism, RBM20 disease origin in induced Pluripotent Stem Cells (iPSCs), and RBM20 mutations in dilated cardiomyopathy. In the end, we will discuss the multifunctional role of RBM20 and manipulation of RBM20 as a potential therapeutic target for heart disease. MDPI 2018-01-05 /pmc/articles/PMC5793171/ /pubmed/29304022 http://dx.doi.org/10.3390/genes9010018 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Rexiati, Maimaiti
Sun, Mingming
Guo, Wei
Muscle-Specific Mis-Splicing and Heart Disease Exemplified by RBM20
title Muscle-Specific Mis-Splicing and Heart Disease Exemplified by RBM20
title_full Muscle-Specific Mis-Splicing and Heart Disease Exemplified by RBM20
title_fullStr Muscle-Specific Mis-Splicing and Heart Disease Exemplified by RBM20
title_full_unstemmed Muscle-Specific Mis-Splicing and Heart Disease Exemplified by RBM20
title_short Muscle-Specific Mis-Splicing and Heart Disease Exemplified by RBM20
title_sort muscle-specific mis-splicing and heart disease exemplified by rbm20
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793171/
https://www.ncbi.nlm.nih.gov/pubmed/29304022
http://dx.doi.org/10.3390/genes9010018
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