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Implications of CpG islands on chromosomal architectures and modes of global gene regulation

CpG islands (CGIs) have long been implicated in the regulation of vertebrate gene expression. However, the involvement of CGIs in chromosomal architectures and associated gene expression regulations has not yet been thoroughly explored. By combining large-scale integrative data analyses and experime...

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Autores principales: Beck, Samuel, Rhee, Catherine, Song, Jawon, Lee, Bum-Kyu, LeBlanc, Lucy, Cannon, Laurie, Kim, Jonghwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5961348/
https://www.ncbi.nlm.nih.gov/pubmed/29529258
http://dx.doi.org/10.1093/nar/gky147
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author Beck, Samuel
Rhee, Catherine
Song, Jawon
Lee, Bum-Kyu
LeBlanc, Lucy
Cannon, Laurie
Kim, Jonghwan
author_facet Beck, Samuel
Rhee, Catherine
Song, Jawon
Lee, Bum-Kyu
LeBlanc, Lucy
Cannon, Laurie
Kim, Jonghwan
author_sort Beck, Samuel
collection PubMed
description CpG islands (CGIs) have long been implicated in the regulation of vertebrate gene expression. However, the involvement of CGIs in chromosomal architectures and associated gene expression regulations has not yet been thoroughly explored. By combining large-scale integrative data analyses and experimental validations, we show that CGIs clearly reconcile two competing models explaining nuclear gene localizations. We first identify CGI-containing (CGI+) and CGI-less (CGI−) genes are non-randomly clustered within the genome, which reflects CGI-dependent spatial gene segregation in the nucleus and corresponding gene regulatory modes. Regardless of their transcriptional activities, CGI+ genes are mainly located at the nuclear center and encounter frequent long-range chromosomal interactions. Meanwhile, nuclear peripheral CGI− genes forming heterochromatin are activated and internalized into the nuclear center by local enhancer–promoter interactions. Our findings demonstrate the crucial implications of CGIs on chromosomal architectures and gene positioning, linking the critical importance of CGIs in determining distinct mechanisms of global gene regulation in three-dimensional space in the nucleus.
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spelling pubmed-59613482018-06-06 Implications of CpG islands on chromosomal architectures and modes of global gene regulation Beck, Samuel Rhee, Catherine Song, Jawon Lee, Bum-Kyu LeBlanc, Lucy Cannon, Laurie Kim, Jonghwan Nucleic Acids Res Gene regulation, Chromatin and Epigenetics CpG islands (CGIs) have long been implicated in the regulation of vertebrate gene expression. However, the involvement of CGIs in chromosomal architectures and associated gene expression regulations has not yet been thoroughly explored. By combining large-scale integrative data analyses and experimental validations, we show that CGIs clearly reconcile two competing models explaining nuclear gene localizations. We first identify CGI-containing (CGI+) and CGI-less (CGI−) genes are non-randomly clustered within the genome, which reflects CGI-dependent spatial gene segregation in the nucleus and corresponding gene regulatory modes. Regardless of their transcriptional activities, CGI+ genes are mainly located at the nuclear center and encounter frequent long-range chromosomal interactions. Meanwhile, nuclear peripheral CGI− genes forming heterochromatin are activated and internalized into the nuclear center by local enhancer–promoter interactions. Our findings demonstrate the crucial implications of CGIs on chromosomal architectures and gene positioning, linking the critical importance of CGIs in determining distinct mechanisms of global gene regulation in three-dimensional space in the nucleus. Oxford University Press 2018-05-18 2018-02-26 /pmc/articles/PMC5961348/ /pubmed/29529258 http://dx.doi.org/10.1093/nar/gky147 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Gene regulation, Chromatin and Epigenetics
Beck, Samuel
Rhee, Catherine
Song, Jawon
Lee, Bum-Kyu
LeBlanc, Lucy
Cannon, Laurie
Kim, Jonghwan
Implications of CpG islands on chromosomal architectures and modes of global gene regulation
title Implications of CpG islands on chromosomal architectures and modes of global gene regulation
title_full Implications of CpG islands on chromosomal architectures and modes of global gene regulation
title_fullStr Implications of CpG islands on chromosomal architectures and modes of global gene regulation
title_full_unstemmed Implications of CpG islands on chromosomal architectures and modes of global gene regulation
title_short Implications of CpG islands on chromosomal architectures and modes of global gene regulation
title_sort implications of cpg islands on chromosomal architectures and modes of global gene regulation
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5961348/
https://www.ncbi.nlm.nih.gov/pubmed/29529258
http://dx.doi.org/10.1093/nar/gky147
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