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Analysis of epigenetic stability and conversions in Saccharomyces cerevisiae reveals a novel role of CAF-I in position-effect variegation
Position-effect variegation (PEV) phenotypes are characterized by the robust multigenerational repression of a gene located at a certain locus (often called gene silencing) and occasional conversions to fully active state. Consequently, the active state then persists with occasional conversions to t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794585/ https://www.ncbi.nlm.nih.gov/pubmed/23863839 http://dx.doi.org/10.1093/nar/gkt623 |
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author | Jeffery, Daniel C. B. Wyse, Brandon A. Rehman, Muhammad Attiq Brown, Geoffrey W. You, Zhiying Oshidari, Roxanne Masai, Hisao Yankulov, Krassimir Y. |
author_facet | Jeffery, Daniel C. B. Wyse, Brandon A. Rehman, Muhammad Attiq Brown, Geoffrey W. You, Zhiying Oshidari, Roxanne Masai, Hisao Yankulov, Krassimir Y. |
author_sort | Jeffery, Daniel C. B. |
collection | PubMed |
description | Position-effect variegation (PEV) phenotypes are characterized by the robust multigenerational repression of a gene located at a certain locus (often called gene silencing) and occasional conversions to fully active state. Consequently, the active state then persists with occasional conversions to the repressed state. These effects are mediated by the establishment and maintenance of heterochromatin or euchromatin structures, respectively. In this study, we have addressed an important but often neglected aspect of PEV: the frequency of conversions at such loci. We have developed a model and have projected various PEV scenarios based on various rates of conversions. We have also enhanced two existing assays for gene silencing in Saccharomyces cerevisiae to measure the rate of switches from repressed to active state and vice versa. We tested the validity of our methodology in Δsir1 cells and in several mutants with defects in gene silencing. The assays have revealed that the histone chaperone Chromatin Assembly Factor I is involved in the control of epigenetic conversions. Together, our model and assays provide a comprehensive methodology for further investigation of epigenetic stability and position effects. |
format | Online Article Text |
id | pubmed-3794585 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37945852013-10-21 Analysis of epigenetic stability and conversions in Saccharomyces cerevisiae reveals a novel role of CAF-I in position-effect variegation Jeffery, Daniel C. B. Wyse, Brandon A. Rehman, Muhammad Attiq Brown, Geoffrey W. You, Zhiying Oshidari, Roxanne Masai, Hisao Yankulov, Krassimir Y. Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics Position-effect variegation (PEV) phenotypes are characterized by the robust multigenerational repression of a gene located at a certain locus (often called gene silencing) and occasional conversions to fully active state. Consequently, the active state then persists with occasional conversions to the repressed state. These effects are mediated by the establishment and maintenance of heterochromatin or euchromatin structures, respectively. In this study, we have addressed an important but often neglected aspect of PEV: the frequency of conversions at such loci. We have developed a model and have projected various PEV scenarios based on various rates of conversions. We have also enhanced two existing assays for gene silencing in Saccharomyces cerevisiae to measure the rate of switches from repressed to active state and vice versa. We tested the validity of our methodology in Δsir1 cells and in several mutants with defects in gene silencing. The assays have revealed that the histone chaperone Chromatin Assembly Factor I is involved in the control of epigenetic conversions. Together, our model and assays provide a comprehensive methodology for further investigation of epigenetic stability and position effects. Oxford University Press 2013-10 2013-07-17 /pmc/articles/PMC3794585/ /pubmed/23863839 http://dx.doi.org/10.1093/nar/gkt623 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene Regulation, Chromatin and Epigenetics Jeffery, Daniel C. B. Wyse, Brandon A. Rehman, Muhammad Attiq Brown, Geoffrey W. You, Zhiying Oshidari, Roxanne Masai, Hisao Yankulov, Krassimir Y. Analysis of epigenetic stability and conversions in Saccharomyces cerevisiae reveals a novel role of CAF-I in position-effect variegation |
title | Analysis of epigenetic stability and conversions in Saccharomyces cerevisiae reveals a novel role of CAF-I in position-effect variegation |
title_full | Analysis of epigenetic stability and conversions in Saccharomyces cerevisiae reveals a novel role of CAF-I in position-effect variegation |
title_fullStr | Analysis of epigenetic stability and conversions in Saccharomyces cerevisiae reveals a novel role of CAF-I in position-effect variegation |
title_full_unstemmed | Analysis of epigenetic stability and conversions in Saccharomyces cerevisiae reveals a novel role of CAF-I in position-effect variegation |
title_short | Analysis of epigenetic stability and conversions in Saccharomyces cerevisiae reveals a novel role of CAF-I in position-effect variegation |
title_sort | analysis of epigenetic stability and conversions in saccharomyces cerevisiae reveals a novel role of caf-i in position-effect variegation |
topic | Gene Regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794585/ https://www.ncbi.nlm.nih.gov/pubmed/23863839 http://dx.doi.org/10.1093/nar/gkt623 |
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