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Reduced PRC2 function alters male germline epigenetic programming and paternal inheritance

BACKGROUND: Defining the mechanisms that establish and regulate the transmission of epigenetic information from parent to offspring is critical for understanding disease heredity. Currently, the molecular pathways that regulate epigenetic information in the germline and its transmission to offspring...

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Autores principales: Stringer, Jessica M., Forster, Samuel C., Qu, Zhipeng, Prokopuk, Lexie, O’Bryan, Moira K., Gardner, David K., White, Stefan J., Adelson, David, Western, Patrick S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149058/
https://www.ncbi.nlm.nih.gov/pubmed/30236109
http://dx.doi.org/10.1186/s12915-018-0569-5
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author Stringer, Jessica M.
Forster, Samuel C.
Qu, Zhipeng
Prokopuk, Lexie
O’Bryan, Moira K.
Gardner, David K.
White, Stefan J.
Adelson, David
Western, Patrick S.
author_facet Stringer, Jessica M.
Forster, Samuel C.
Qu, Zhipeng
Prokopuk, Lexie
O’Bryan, Moira K.
Gardner, David K.
White, Stefan J.
Adelson, David
Western, Patrick S.
author_sort Stringer, Jessica M.
collection PubMed
description BACKGROUND: Defining the mechanisms that establish and regulate the transmission of epigenetic information from parent to offspring is critical for understanding disease heredity. Currently, the molecular pathways that regulate epigenetic information in the germline and its transmission to offspring are poorly understood. RESULTS: Here we provide evidence that Polycomb Repressive Complex 2 (PRC2) regulates paternal inheritance. Reduced PRC2 function in mice resulted in male sub-fertility and altered epigenetic and transcriptional control of retrotransposed elements in foetal male germ cells. Males with reduced PRC2 function produced offspring that over-expressed retrotransposed pseudogenes and had altered preimplantation embryo cleavage rates and cell cycle control. CONCLUSION: This study reveals a novel role for the histone-modifying complex, PRC2, in paternal intergenerational transmission of epigenetic effects on offspring, with important implications for understanding disease inheritance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-018-0569-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-61490582018-09-26 Reduced PRC2 function alters male germline epigenetic programming and paternal inheritance Stringer, Jessica M. Forster, Samuel C. Qu, Zhipeng Prokopuk, Lexie O’Bryan, Moira K. Gardner, David K. White, Stefan J. Adelson, David Western, Patrick S. BMC Biol Research Article BACKGROUND: Defining the mechanisms that establish and regulate the transmission of epigenetic information from parent to offspring is critical for understanding disease heredity. Currently, the molecular pathways that regulate epigenetic information in the germline and its transmission to offspring are poorly understood. RESULTS: Here we provide evidence that Polycomb Repressive Complex 2 (PRC2) regulates paternal inheritance. Reduced PRC2 function in mice resulted in male sub-fertility and altered epigenetic and transcriptional control of retrotransposed elements in foetal male germ cells. Males with reduced PRC2 function produced offspring that over-expressed retrotransposed pseudogenes and had altered preimplantation embryo cleavage rates and cell cycle control. CONCLUSION: This study reveals a novel role for the histone-modifying complex, PRC2, in paternal intergenerational transmission of epigenetic effects on offspring, with important implications for understanding disease inheritance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-018-0569-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-20 /pmc/articles/PMC6149058/ /pubmed/30236109 http://dx.doi.org/10.1186/s12915-018-0569-5 Text en © Western et al. 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Stringer, Jessica M.
Forster, Samuel C.
Qu, Zhipeng
Prokopuk, Lexie
O’Bryan, Moira K.
Gardner, David K.
White, Stefan J.
Adelson, David
Western, Patrick S.
Reduced PRC2 function alters male germline epigenetic programming and paternal inheritance
title Reduced PRC2 function alters male germline epigenetic programming and paternal inheritance
title_full Reduced PRC2 function alters male germline epigenetic programming and paternal inheritance
title_fullStr Reduced PRC2 function alters male germline epigenetic programming and paternal inheritance
title_full_unstemmed Reduced PRC2 function alters male germline epigenetic programming and paternal inheritance
title_short Reduced PRC2 function alters male germline epigenetic programming and paternal inheritance
title_sort reduced prc2 function alters male germline epigenetic programming and paternal inheritance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149058/
https://www.ncbi.nlm.nih.gov/pubmed/30236109
http://dx.doi.org/10.1186/s12915-018-0569-5
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