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Maintaining memory of silencing at imprinted differentially methylated regions
Imprinted genes are an exceptional cluster of genes which are expressed in a parent-of-origin dependent fashion. This allele-specific expression is dependent on differential DNA methylation which is established in the parental germlines in a sex-specific manner. The DNA methylation imprint is accomp...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819931/ https://www.ncbi.nlm.nih.gov/pubmed/26883803 http://dx.doi.org/10.1007/s00018-016-2157-6 |
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author | Voon, Hsiao P. J. Gibbons, Richard J. |
author_facet | Voon, Hsiao P. J. Gibbons, Richard J. |
author_sort | Voon, Hsiao P. J. |
collection | PubMed |
description | Imprinted genes are an exceptional cluster of genes which are expressed in a parent-of-origin dependent fashion. This allele-specific expression is dependent on differential DNA methylation which is established in the parental germlines in a sex-specific manner. The DNA methylation imprint is accompanied by heterochromatin modifications which must be continuously maintained through development. This review summarises the factors which are important for protecting the epigenetic modifications at imprinted differentially methylated regions (DMRs), including PGC7, ZFP57 and the ATRX/Daxx/H3.3 complex. We discuss how these factors maintain heterochromatin silencing, not only at imprinted DMRs, but also other heterochromatic regions in the genome. |
format | Online Article Text |
id | pubmed-4819931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-48199312016-04-11 Maintaining memory of silencing at imprinted differentially methylated regions Voon, Hsiao P. J. Gibbons, Richard J. Cell Mol Life Sci Review Imprinted genes are an exceptional cluster of genes which are expressed in a parent-of-origin dependent fashion. This allele-specific expression is dependent on differential DNA methylation which is established in the parental germlines in a sex-specific manner. The DNA methylation imprint is accompanied by heterochromatin modifications which must be continuously maintained through development. This review summarises the factors which are important for protecting the epigenetic modifications at imprinted differentially methylated regions (DMRs), including PGC7, ZFP57 and the ATRX/Daxx/H3.3 complex. We discuss how these factors maintain heterochromatin silencing, not only at imprinted DMRs, but also other heterochromatic regions in the genome. Springer International Publishing 2016-02-16 2016 /pmc/articles/PMC4819931/ /pubmed/26883803 http://dx.doi.org/10.1007/s00018-016-2157-6 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Review Voon, Hsiao P. J. Gibbons, Richard J. Maintaining memory of silencing at imprinted differentially methylated regions |
title | Maintaining memory of silencing at imprinted differentially methylated regions |
title_full | Maintaining memory of silencing at imprinted differentially methylated regions |
title_fullStr | Maintaining memory of silencing at imprinted differentially methylated regions |
title_full_unstemmed | Maintaining memory of silencing at imprinted differentially methylated regions |
title_short | Maintaining memory of silencing at imprinted differentially methylated regions |
title_sort | maintaining memory of silencing at imprinted differentially methylated regions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819931/ https://www.ncbi.nlm.nih.gov/pubmed/26883803 http://dx.doi.org/10.1007/s00018-016-2157-6 |
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