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Imprinted silencing is extended over broad chromosomal domains in mouse extra-embryonic lineages
Gene silencing in imprinted gene clusters is established by an epigenetic initiator that is often a long non-coding (lnc) RNA. The clustered organization of known imprinted genes indicates that the initiator extends imprinted silencing over broader chromosomal domains in extra-embryonic lineages com...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695569/ https://www.ncbi.nlm.nih.gov/pubmed/23478214 http://dx.doi.org/10.1016/j.ceb.2013.02.012 |
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author | Kulinski, Tomasz M Barlow, Denise P Hudson, Quanah J |
author_facet | Kulinski, Tomasz M Barlow, Denise P Hudson, Quanah J |
author_sort | Kulinski, Tomasz M |
collection | PubMed |
description | Gene silencing in imprinted gene clusters is established by an epigenetic initiator that is often a long non-coding (lnc) RNA. The clustered organization of known imprinted genes indicates that the initiator extends imprinted silencing over broader chromosomal domains in extra-embryonic lineages compared to the embryo. We propose that extension of imprinted gene clusters may result from known epigenetic differences between extra-embryonic and embryonic lineages that alter the behavior of epigenetic initiators. New RNA sequencing technology will enable the full extent of imprinted silencing in embryonic and extra-embryonic lineages to be defined, but appropriate analysis and cell systems are required, which we define here based on a review of recent studies. |
format | Online Article Text |
id | pubmed-3695569 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-36955692013-06-28 Imprinted silencing is extended over broad chromosomal domains in mouse extra-embryonic lineages Kulinski, Tomasz M Barlow, Denise P Hudson, Quanah J Curr Opin Cell Biol Article Gene silencing in imprinted gene clusters is established by an epigenetic initiator that is often a long non-coding (lnc) RNA. The clustered organization of known imprinted genes indicates that the initiator extends imprinted silencing over broader chromosomal domains in extra-embryonic lineages compared to the embryo. We propose that extension of imprinted gene clusters may result from known epigenetic differences between extra-embryonic and embryonic lineages that alter the behavior of epigenetic initiators. New RNA sequencing technology will enable the full extent of imprinted silencing in embryonic and extra-embryonic lineages to be defined, but appropriate analysis and cell systems are required, which we define here based on a review of recent studies. Elsevier 2013-06 /pmc/articles/PMC3695569/ /pubmed/23478214 http://dx.doi.org/10.1016/j.ceb.2013.02.012 Text en © 2013 Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license |
spellingShingle | Article Kulinski, Tomasz M Barlow, Denise P Hudson, Quanah J Imprinted silencing is extended over broad chromosomal domains in mouse extra-embryonic lineages |
title | Imprinted silencing is extended over broad chromosomal domains in mouse extra-embryonic lineages |
title_full | Imprinted silencing is extended over broad chromosomal domains in mouse extra-embryonic lineages |
title_fullStr | Imprinted silencing is extended over broad chromosomal domains in mouse extra-embryonic lineages |
title_full_unstemmed | Imprinted silencing is extended over broad chromosomal domains in mouse extra-embryonic lineages |
title_short | Imprinted silencing is extended over broad chromosomal domains in mouse extra-embryonic lineages |
title_sort | imprinted silencing is extended over broad chromosomal domains in mouse extra-embryonic lineages |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695569/ https://www.ncbi.nlm.nih.gov/pubmed/23478214 http://dx.doi.org/10.1016/j.ceb.2013.02.012 |
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