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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
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.
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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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