Cargando…

Sperm-inherited H3K27me3 impacts offspring transcription and development in C. elegans

Paternal epigenetic inheritance is gaining attention for its growing medical relevance. However, the form in which paternal epigenetic information is transmitted to offspring and how it influences offspring development remain poorly understood. Here we show that in C. elegans, sperm-inherited chroma...

Descripción completa

Detalles Bibliográficos
Autores principales: Kaneshiro, Kiyomi Raye, Rechtsteiner, Andreas, Strome, Susan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426959/
https://www.ncbi.nlm.nih.gov/pubmed/30894520
http://dx.doi.org/10.1038/s41467-019-09141-w
_version_ 1783405106182488064
author Kaneshiro, Kiyomi Raye
Rechtsteiner, Andreas
Strome, Susan
author_facet Kaneshiro, Kiyomi Raye
Rechtsteiner, Andreas
Strome, Susan
author_sort Kaneshiro, Kiyomi Raye
collection PubMed
description Paternal epigenetic inheritance is gaining attention for its growing medical relevance. However, the form in which paternal epigenetic information is transmitted to offspring and how it influences offspring development remain poorly understood. Here we show that in C. elegans, sperm-inherited chromatin states transmitted to the primordial germ cells in offspring influence germline transcription and development. We show that sperm chromosomes inherited lacking the repressive histone modification H3K27me3 are maintained in that state by H3K36me3 antagonism. Inheritance of H3K27me3-lacking sperm chromosomes results in derepression in the germline of somatic genes, especially neuronal genes, predominantly from sperm-inherited alleles. This results in germ cells primed for losing their germ cell identity and adopting a neuronal fate. These data demonstrate that histone modifications are one mechanism through which epigenetic information from a father can shape offspring gene expression and development.
format Online
Article
Text
id pubmed-6426959
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-64269592019-03-22 Sperm-inherited H3K27me3 impacts offspring transcription and development in C. elegans Kaneshiro, Kiyomi Raye Rechtsteiner, Andreas Strome, Susan Nat Commun Article Paternal epigenetic inheritance is gaining attention for its growing medical relevance. However, the form in which paternal epigenetic information is transmitted to offspring and how it influences offspring development remain poorly understood. Here we show that in C. elegans, sperm-inherited chromatin states transmitted to the primordial germ cells in offspring influence germline transcription and development. We show that sperm chromosomes inherited lacking the repressive histone modification H3K27me3 are maintained in that state by H3K36me3 antagonism. Inheritance of H3K27me3-lacking sperm chromosomes results in derepression in the germline of somatic genes, especially neuronal genes, predominantly from sperm-inherited alleles. This results in germ cells primed for losing their germ cell identity and adopting a neuronal fate. These data demonstrate that histone modifications are one mechanism through which epigenetic information from a father can shape offspring gene expression and development. Nature Publishing Group UK 2019-03-20 /pmc/articles/PMC6426959/ /pubmed/30894520 http://dx.doi.org/10.1038/s41467-019-09141-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kaneshiro, Kiyomi Raye
Rechtsteiner, Andreas
Strome, Susan
Sperm-inherited H3K27me3 impacts offspring transcription and development in C. elegans
title Sperm-inherited H3K27me3 impacts offspring transcription and development in C. elegans
title_full Sperm-inherited H3K27me3 impacts offspring transcription and development in C. elegans
title_fullStr Sperm-inherited H3K27me3 impacts offspring transcription and development in C. elegans
title_full_unstemmed Sperm-inherited H3K27me3 impacts offspring transcription and development in C. elegans
title_short Sperm-inherited H3K27me3 impacts offspring transcription and development in C. elegans
title_sort sperm-inherited h3k27me3 impacts offspring transcription and development in c. elegans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426959/
https://www.ncbi.nlm.nih.gov/pubmed/30894520
http://dx.doi.org/10.1038/s41467-019-09141-w
work_keys_str_mv AT kaneshirokiyomiraye sperminheritedh3k27me3impactsoffspringtranscriptionanddevelopmentincelegans
AT rechtsteinerandreas sperminheritedh3k27me3impactsoffspringtranscriptionanddevelopmentincelegans
AT stromesusan sperminheritedh3k27me3impactsoffspringtranscriptionanddevelopmentincelegans