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Combinatorial Pattern of Histone Modifications in Exon Skipping Event

Histone modifications are associated with alternative splicing. It has been suggested that histone modifications act in combinational patterns in gene expression regulation. However, how they interact with each other and what is their casual relationships in the process of RNA splicing remain unclea...

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Detalles Bibliográficos
Autores principales: Chen, Wei, Song, Xiaoming, Lin, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387913/
https://www.ncbi.nlm.nih.gov/pubmed/30833963
http://dx.doi.org/10.3389/fgene.2019.00122
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author Chen, Wei
Song, Xiaoming
Lin, Hao
author_facet Chen, Wei
Song, Xiaoming
Lin, Hao
author_sort Chen, Wei
collection PubMed
description Histone modifications are associated with alternative splicing. It has been suggested that histone modifications act in combinational patterns in gene expression regulation. However, how they interact with each other and what is their casual relationships in the process of RNA splicing remain unclear. In this study, the combinatorial patterns of 38 kinds of histone modifications in the exon skipping event of the CD4(+) T cell were analyzed by constructing Bayesian networks. Distinct combinatorial patterns of histone modifications that illustrating their casual relationships were observed in excluded/included exons and the surrounding intronic regions. The Bayesian networks also indicate that some histone modifications directly correlate with RNA splicing. We anticipate that this work could provide novel insights into the effects of histone modifications on RNA splicing regulation.
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spelling pubmed-63879132019-03-04 Combinatorial Pattern of Histone Modifications in Exon Skipping Event Chen, Wei Song, Xiaoming Lin, Hao Front Genet Genetics Histone modifications are associated with alternative splicing. It has been suggested that histone modifications act in combinational patterns in gene expression regulation. However, how they interact with each other and what is their casual relationships in the process of RNA splicing remain unclear. In this study, the combinatorial patterns of 38 kinds of histone modifications in the exon skipping event of the CD4(+) T cell were analyzed by constructing Bayesian networks. Distinct combinatorial patterns of histone modifications that illustrating their casual relationships were observed in excluded/included exons and the surrounding intronic regions. The Bayesian networks also indicate that some histone modifications directly correlate with RNA splicing. We anticipate that this work could provide novel insights into the effects of histone modifications on RNA splicing regulation. Frontiers Media S.A. 2019-02-18 /pmc/articles/PMC6387913/ /pubmed/30833963 http://dx.doi.org/10.3389/fgene.2019.00122 Text en Copyright © 2019 Chen, Song and Lin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Chen, Wei
Song, Xiaoming
Lin, Hao
Combinatorial Pattern of Histone Modifications in Exon Skipping Event
title Combinatorial Pattern of Histone Modifications in Exon Skipping Event
title_full Combinatorial Pattern of Histone Modifications in Exon Skipping Event
title_fullStr Combinatorial Pattern of Histone Modifications in Exon Skipping Event
title_full_unstemmed Combinatorial Pattern of Histone Modifications in Exon Skipping Event
title_short Combinatorial Pattern of Histone Modifications in Exon Skipping Event
title_sort combinatorial pattern of histone modifications in exon skipping event
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387913/
https://www.ncbi.nlm.nih.gov/pubmed/30833963
http://dx.doi.org/10.3389/fgene.2019.00122
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