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Bioinformatics challenges and perspectives when studying the effect of epigenetic modifications on alternative splicing

It is widely known that epigenetic modifications are important in regulating transcription, but several have also been reported in alternative splicing. The regulation of pre-mRNA splicing is important to explain proteomic diversity and the misregulation of splicing has been implicated in many disea...

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Detalles Bibliográficos
Autores principales: Pacini, Clare, Koziol, Magdalena J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915717/
https://www.ncbi.nlm.nih.gov/pubmed/29685977
http://dx.doi.org/10.1098/rstb.2017.0073
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author Pacini, Clare
Koziol, Magdalena J.
author_facet Pacini, Clare
Koziol, Magdalena J.
author_sort Pacini, Clare
collection PubMed
description It is widely known that epigenetic modifications are important in regulating transcription, but several have also been reported in alternative splicing. The regulation of pre-mRNA splicing is important to explain proteomic diversity and the misregulation of splicing has been implicated in many diseases. Here, we give a brief overview of the role of epigenetics in alternative splicing and disease. We then discuss the bioinformatics methods that can be used to model interactions between epigenetic marks and regulators of splicing. These models can be used to identify alternative splicing and epigenetic changes across different phenotypes. This article is part of a discussion meeting issue ‘Frontiers in epigenetic chemical biology’.
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spelling pubmed-59157172018-04-27 Bioinformatics challenges and perspectives when studying the effect of epigenetic modifications on alternative splicing Pacini, Clare Koziol, Magdalena J. Philos Trans R Soc Lond B Biol Sci Articles It is widely known that epigenetic modifications are important in regulating transcription, but several have also been reported in alternative splicing. The regulation of pre-mRNA splicing is important to explain proteomic diversity and the misregulation of splicing has been implicated in many diseases. Here, we give a brief overview of the role of epigenetics in alternative splicing and disease. We then discuss the bioinformatics methods that can be used to model interactions between epigenetic marks and regulators of splicing. These models can be used to identify alternative splicing and epigenetic changes across different phenotypes. This article is part of a discussion meeting issue ‘Frontiers in epigenetic chemical biology’. The Royal Society 2018-06-05 2018-04-23 /pmc/articles/PMC5915717/ /pubmed/29685977 http://dx.doi.org/10.1098/rstb.2017.0073 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Articles
Pacini, Clare
Koziol, Magdalena J.
Bioinformatics challenges and perspectives when studying the effect of epigenetic modifications on alternative splicing
title Bioinformatics challenges and perspectives when studying the effect of epigenetic modifications on alternative splicing
title_full Bioinformatics challenges and perspectives when studying the effect of epigenetic modifications on alternative splicing
title_fullStr Bioinformatics challenges and perspectives when studying the effect of epigenetic modifications on alternative splicing
title_full_unstemmed Bioinformatics challenges and perspectives when studying the effect of epigenetic modifications on alternative splicing
title_short Bioinformatics challenges and perspectives when studying the effect of epigenetic modifications on alternative splicing
title_sort bioinformatics challenges and perspectives when studying the effect of epigenetic modifications on alternative splicing
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915717/
https://www.ncbi.nlm.nih.gov/pubmed/29685977
http://dx.doi.org/10.1098/rstb.2017.0073
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