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Chromatin analysis of occluded genes
We recently described two opposing states of transcriptional competency. One is termed ‘competent’ whereby a gene is capable of responding to trans-acting transcription factors of the cell, such that it is active if appropriate transcriptional activators are present, though it can also be silent if...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2701328/ https://www.ncbi.nlm.nih.gov/pubmed/19380460 http://dx.doi.org/10.1093/hmg/ddp188 |
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author | Lee, Jae Hyun Gaetz, Jedidiah Bugarija, Branimir Fernandes, Croydon J. Snyder, Gregory E. Bush, Eliot C. Lahn, Bruce T. |
author_facet | Lee, Jae Hyun Gaetz, Jedidiah Bugarija, Branimir Fernandes, Croydon J. Snyder, Gregory E. Bush, Eliot C. Lahn, Bruce T. |
author_sort | Lee, Jae Hyun |
collection | PubMed |
description | We recently described two opposing states of transcriptional competency. One is termed ‘competent’ whereby a gene is capable of responding to trans-acting transcription factors of the cell, such that it is active if appropriate transcriptional activators are present, though it can also be silent if activators are absent or repressors are present. The other is termed ‘occluded’ whereby a gene is silenced by cis-acting, chromatin-based mechanisms in a manner that blocks it from responding to trans-acting factors, such that it is silent even when activators are present in the cellular milieu. We proposed that gene occlusion is a mechanism by which differentiated cells stably maintain their phenotypic identities. Here, we describe chromatin analysis of occluded genes. We found that DNA methylation plays a causal role in maintaining occlusion for a subset of occluded genes. We further examined a variety of other chromatin marks typically associated with transcriptional silencing, including histone variants, covalent histone modifications and chromatin-associated proteins. Surprisingly, we found that although many of these marks are robustly linked to silent genes (which include both occluded genes and genes that are competent but silent), none is linked specifically to occluded genes. Although the observation does not rule out a possible causal role of these chromatin marks in occlusion, it does suggest that these marks might be secondary effect rather than primary cause of the silent state in many genes. |
format | Text |
id | pubmed-2701328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27013282009-06-25 Chromatin analysis of occluded genes Lee, Jae Hyun Gaetz, Jedidiah Bugarija, Branimir Fernandes, Croydon J. Snyder, Gregory E. Bush, Eliot C. Lahn, Bruce T. Hum Mol Genet Articles We recently described two opposing states of transcriptional competency. One is termed ‘competent’ whereby a gene is capable of responding to trans-acting transcription factors of the cell, such that it is active if appropriate transcriptional activators are present, though it can also be silent if activators are absent or repressors are present. The other is termed ‘occluded’ whereby a gene is silenced by cis-acting, chromatin-based mechanisms in a manner that blocks it from responding to trans-acting factors, such that it is silent even when activators are present in the cellular milieu. We proposed that gene occlusion is a mechanism by which differentiated cells stably maintain their phenotypic identities. Here, we describe chromatin analysis of occluded genes. We found that DNA methylation plays a causal role in maintaining occlusion for a subset of occluded genes. We further examined a variety of other chromatin marks typically associated with transcriptional silencing, including histone variants, covalent histone modifications and chromatin-associated proteins. Surprisingly, we found that although many of these marks are robustly linked to silent genes (which include both occluded genes and genes that are competent but silent), none is linked specifically to occluded genes. Although the observation does not rule out a possible causal role of these chromatin marks in occlusion, it does suggest that these marks might be secondary effect rather than primary cause of the silent state in many genes. Oxford University Press 2009-07-15 2009-04-20 /pmc/articles/PMC2701328/ /pubmed/19380460 http://dx.doi.org/10.1093/hmg/ddp188 Text en © 2009 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Lee, Jae Hyun Gaetz, Jedidiah Bugarija, Branimir Fernandes, Croydon J. Snyder, Gregory E. Bush, Eliot C. Lahn, Bruce T. Chromatin analysis of occluded genes |
title | Chromatin analysis of occluded genes |
title_full | Chromatin analysis of occluded genes |
title_fullStr | Chromatin analysis of occluded genes |
title_full_unstemmed | Chromatin analysis of occluded genes |
title_short | Chromatin analysis of occluded genes |
title_sort | chromatin analysis of occluded genes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2701328/ https://www.ncbi.nlm.nih.gov/pubmed/19380460 http://dx.doi.org/10.1093/hmg/ddp188 |
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