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Epigenetic and Transcriptional Alterations in Human Adipose Tissue of Polycystic Ovary Syndrome

Genetic and epigenetic factors may predispose women to polycystic ovary syndrome (PCOS), a common heritable disorder of unclear etiology. Here we investigated differences in genome-wide gene expression and DNA methylation in adipose tissue from 64 women with PCOS and 30 controls. In total, 1720 uniq...

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Autores principales: Kokosar, Milana, Benrick, Anna, Perfilyev, Alexander, Fornes, Romina, Nilsson, Emma, Maliqueo, Manuel, Behre, Carl Johan, Sazonova, Antonina, Ohlsson, Claes, Ling, Charlotte, Stener-Victorin, Elisabet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4791632/
https://www.ncbi.nlm.nih.gov/pubmed/26975253
http://dx.doi.org/10.1038/srep22883
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author Kokosar, Milana
Benrick, Anna
Perfilyev, Alexander
Fornes, Romina
Nilsson, Emma
Maliqueo, Manuel
Behre, Carl Johan
Sazonova, Antonina
Ohlsson, Claes
Ling, Charlotte
Stener-Victorin, Elisabet
author_facet Kokosar, Milana
Benrick, Anna
Perfilyev, Alexander
Fornes, Romina
Nilsson, Emma
Maliqueo, Manuel
Behre, Carl Johan
Sazonova, Antonina
Ohlsson, Claes
Ling, Charlotte
Stener-Victorin, Elisabet
author_sort Kokosar, Milana
collection PubMed
description Genetic and epigenetic factors may predispose women to polycystic ovary syndrome (PCOS), a common heritable disorder of unclear etiology. Here we investigated differences in genome-wide gene expression and DNA methylation in adipose tissue from 64 women with PCOS and 30 controls. In total, 1720 unique genes were differentially expressed (Q < 0.05). Six out of twenty selected genes with largest expression difference (CYP1B1, GPT), genes linked to PCOS (RAB5B) or type 2 diabetes (PPARG, SVEP1), and methylation (DMAP1) were replicated in a separate case-control study. In total, 63,213 sites (P < 0.05) and 440 sites (Q < 0.15) were differently methylated. Thirty differentially expressed genes had corresponding changes in 33 different DNA methylation sites. Moreover, a total number of 1913 pairs of differentially expressed “gene-CpG” probes were significantly correlated after correction for multiple testing and corresponded with 349 unique genes. In conclusion, we identified a large number of genes and pathways that are affected in adipose tissue from women with PCOS. We also identified specific DNA methylation pathways that may affect mRNA expression. Together, these novel findings show that women with PCOS have multiple transcriptional and epigenetic changes in adipose tissue that are relevant for development of the disease.
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spelling pubmed-47916322016-03-16 Epigenetic and Transcriptional Alterations in Human Adipose Tissue of Polycystic Ovary Syndrome Kokosar, Milana Benrick, Anna Perfilyev, Alexander Fornes, Romina Nilsson, Emma Maliqueo, Manuel Behre, Carl Johan Sazonova, Antonina Ohlsson, Claes Ling, Charlotte Stener-Victorin, Elisabet Sci Rep Article Genetic and epigenetic factors may predispose women to polycystic ovary syndrome (PCOS), a common heritable disorder of unclear etiology. Here we investigated differences in genome-wide gene expression and DNA methylation in adipose tissue from 64 women with PCOS and 30 controls. In total, 1720 unique genes were differentially expressed (Q < 0.05). Six out of twenty selected genes with largest expression difference (CYP1B1, GPT), genes linked to PCOS (RAB5B) or type 2 diabetes (PPARG, SVEP1), and methylation (DMAP1) were replicated in a separate case-control study. In total, 63,213 sites (P < 0.05) and 440 sites (Q < 0.15) were differently methylated. Thirty differentially expressed genes had corresponding changes in 33 different DNA methylation sites. Moreover, a total number of 1913 pairs of differentially expressed “gene-CpG” probes were significantly correlated after correction for multiple testing and corresponded with 349 unique genes. In conclusion, we identified a large number of genes and pathways that are affected in adipose tissue from women with PCOS. We also identified specific DNA methylation pathways that may affect mRNA expression. Together, these novel findings show that women with PCOS have multiple transcriptional and epigenetic changes in adipose tissue that are relevant for development of the disease. Nature Publishing Group 2016-03-15 /pmc/articles/PMC4791632/ /pubmed/26975253 http://dx.doi.org/10.1038/srep22883 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kokosar, Milana
Benrick, Anna
Perfilyev, Alexander
Fornes, Romina
Nilsson, Emma
Maliqueo, Manuel
Behre, Carl Johan
Sazonova, Antonina
Ohlsson, Claes
Ling, Charlotte
Stener-Victorin, Elisabet
Epigenetic and Transcriptional Alterations in Human Adipose Tissue of Polycystic Ovary Syndrome
title Epigenetic and Transcriptional Alterations in Human Adipose Tissue of Polycystic Ovary Syndrome
title_full Epigenetic and Transcriptional Alterations in Human Adipose Tissue of Polycystic Ovary Syndrome
title_fullStr Epigenetic and Transcriptional Alterations in Human Adipose Tissue of Polycystic Ovary Syndrome
title_full_unstemmed Epigenetic and Transcriptional Alterations in Human Adipose Tissue of Polycystic Ovary Syndrome
title_short Epigenetic and Transcriptional Alterations in Human Adipose Tissue of Polycystic Ovary Syndrome
title_sort epigenetic and transcriptional alterations in human adipose tissue of polycystic ovary syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4791632/
https://www.ncbi.nlm.nih.gov/pubmed/26975253
http://dx.doi.org/10.1038/srep22883
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