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Aneuploidy as a cause of impaired chromatin silencing and mating-type specification in budding yeast
Aneuploidy and epigenetic alterations have long been associated with carcinogenesis, but it was unknown whether aneuploidy could disrupt the epigenetic states required for cellular differentiation. In this study, we found that ~3% of random aneuploid karyotypes in yeast disrupt the stable inheritanc...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779231/ https://www.ncbi.nlm.nih.gov/pubmed/28841138 http://dx.doi.org/10.7554/eLife.27991 |
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author | Mulla, Wahid A Seidel, Chris W Zhu, Jin Tsai, Hung-Ji Smith, Sarah E Singh, Pushpendra Bradford, William D McCroskey, Scott Nelliat, Anjali R Conkright, Juliana Peak, Allison Malanowski, Kathryn E Perera, Anoja G Li, Rong |
author_facet | Mulla, Wahid A Seidel, Chris W Zhu, Jin Tsai, Hung-Ji Smith, Sarah E Singh, Pushpendra Bradford, William D McCroskey, Scott Nelliat, Anjali R Conkright, Juliana Peak, Allison Malanowski, Kathryn E Perera, Anoja G Li, Rong |
author_sort | Mulla, Wahid A |
collection | PubMed |
description | Aneuploidy and epigenetic alterations have long been associated with carcinogenesis, but it was unknown whether aneuploidy could disrupt the epigenetic states required for cellular differentiation. In this study, we found that ~3% of random aneuploid karyotypes in yeast disrupt the stable inheritance of silenced chromatin during cell proliferation. Karyotype analysis revealed that this phenotype was significantly correlated with gains of chromosomes III and X. Chromosome X disomy alone was sufficient to disrupt chromatin silencing and yeast mating-type identity as indicated by a lack of growth response to pheromone. The silencing defect was not limited to cryptic mating type loci and was associated with broad changes in histone modifications and chromatin localization of Sir2 histone deacetylase. The chromatin-silencing defect of disome X can be partially recapitulated by an extra copy of several genes on chromosome X. These results suggest that aneuploidy can directly cause epigenetic instability and disrupt cellular differentiation. |
format | Online Article Text |
id | pubmed-5779231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57792312018-01-25 Aneuploidy as a cause of impaired chromatin silencing and mating-type specification in budding yeast Mulla, Wahid A Seidel, Chris W Zhu, Jin Tsai, Hung-Ji Smith, Sarah E Singh, Pushpendra Bradford, William D McCroskey, Scott Nelliat, Anjali R Conkright, Juliana Peak, Allison Malanowski, Kathryn E Perera, Anoja G Li, Rong eLife Cell Biology Aneuploidy and epigenetic alterations have long been associated with carcinogenesis, but it was unknown whether aneuploidy could disrupt the epigenetic states required for cellular differentiation. In this study, we found that ~3% of random aneuploid karyotypes in yeast disrupt the stable inheritance of silenced chromatin during cell proliferation. Karyotype analysis revealed that this phenotype was significantly correlated with gains of chromosomes III and X. Chromosome X disomy alone was sufficient to disrupt chromatin silencing and yeast mating-type identity as indicated by a lack of growth response to pheromone. The silencing defect was not limited to cryptic mating type loci and was associated with broad changes in histone modifications and chromatin localization of Sir2 histone deacetylase. The chromatin-silencing defect of disome X can be partially recapitulated by an extra copy of several genes on chromosome X. These results suggest that aneuploidy can directly cause epigenetic instability and disrupt cellular differentiation. eLife Sciences Publications, Ltd 2017-08-25 /pmc/articles/PMC5779231/ /pubmed/28841138 http://dx.doi.org/10.7554/eLife.27991 Text en © 2017, Mulla et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Mulla, Wahid A Seidel, Chris W Zhu, Jin Tsai, Hung-Ji Smith, Sarah E Singh, Pushpendra Bradford, William D McCroskey, Scott Nelliat, Anjali R Conkright, Juliana Peak, Allison Malanowski, Kathryn E Perera, Anoja G Li, Rong Aneuploidy as a cause of impaired chromatin silencing and mating-type specification in budding yeast |
title | Aneuploidy as a cause of impaired chromatin silencing and mating-type specification in budding yeast |
title_full | Aneuploidy as a cause of impaired chromatin silencing and mating-type specification in budding yeast |
title_fullStr | Aneuploidy as a cause of impaired chromatin silencing and mating-type specification in budding yeast |
title_full_unstemmed | Aneuploidy as a cause of impaired chromatin silencing and mating-type specification in budding yeast |
title_short | Aneuploidy as a cause of impaired chromatin silencing and mating-type specification in budding yeast |
title_sort | aneuploidy as a cause of impaired chromatin silencing and mating-type specification in budding yeast |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779231/ https://www.ncbi.nlm.nih.gov/pubmed/28841138 http://dx.doi.org/10.7554/eLife.27991 |
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