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Endurance training remodels sperm-borne small RNA expression and methylation at neurological gene hotspots

Remodeling of the sperm epigenome by lifestyle factors before conception could account for altered metabolism in the next generation offspring. Here, we hypothesized that endurance training changes the epigenome of human spermatozoa. Using small RNA (sRNA) sequencing and reduced representation bisul...

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Autores principales: Ingerslev, Lars R., Donkin, Ida, Fabre, Odile, Versteyhe, Soetkin, Mechta, Mie, Pattamaprapanont, Pattarawan, Mortensen, Brynjulf, Krarup, Nikolaj Thure, Barrès, Romain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785820/
https://www.ncbi.nlm.nih.gov/pubmed/29416570
http://dx.doi.org/10.1186/s13148-018-0446-7
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author Ingerslev, Lars R.
Donkin, Ida
Fabre, Odile
Versteyhe, Soetkin
Mechta, Mie
Pattamaprapanont, Pattarawan
Mortensen, Brynjulf
Krarup, Nikolaj Thure
Barrès, Romain
author_facet Ingerslev, Lars R.
Donkin, Ida
Fabre, Odile
Versteyhe, Soetkin
Mechta, Mie
Pattamaprapanont, Pattarawan
Mortensen, Brynjulf
Krarup, Nikolaj Thure
Barrès, Romain
author_sort Ingerslev, Lars R.
collection PubMed
description Remodeling of the sperm epigenome by lifestyle factors before conception could account for altered metabolism in the next generation offspring. Here, we hypothesized that endurance training changes the epigenome of human spermatozoa. Using small RNA (sRNA) sequencing and reduced representation bisulfite sequencing (RRBS), we, respectively, investigated sRNA expression and DNA methylation in pure fractions of motile spermatozoa collected from young healthy individuals before, after 6 weeks of endurance training and after 3 months without exercise. Expression of 8 PIWI interacting RNA were changed by exercise training. RRBS analysis revealed 330 differentially methylated regions (DMRs) after training and 303 DMRs after the detraining period, which were, in both conditions, enriched at close vicinity of transcription start sites. Ontology analysis of genes located at proximity of DMRs returned terms related to neurological function at the trained state and, to a much lesser extent, at the detrained state. Our study reveal that short-term endurance training induces marked remodeling of the sperm epigenome, and identify genes related to the development of the central nervous system as potential hot spots for epigenetic variation upon environmental stress. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-018-0446-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-57858202018-02-07 Endurance training remodels sperm-borne small RNA expression and methylation at neurological gene hotspots Ingerslev, Lars R. Donkin, Ida Fabre, Odile Versteyhe, Soetkin Mechta, Mie Pattamaprapanont, Pattarawan Mortensen, Brynjulf Krarup, Nikolaj Thure Barrès, Romain Clin Epigenetics Short Report Remodeling of the sperm epigenome by lifestyle factors before conception could account for altered metabolism in the next generation offspring. Here, we hypothesized that endurance training changes the epigenome of human spermatozoa. Using small RNA (sRNA) sequencing and reduced representation bisulfite sequencing (RRBS), we, respectively, investigated sRNA expression and DNA methylation in pure fractions of motile spermatozoa collected from young healthy individuals before, after 6 weeks of endurance training and after 3 months without exercise. Expression of 8 PIWI interacting RNA were changed by exercise training. RRBS analysis revealed 330 differentially methylated regions (DMRs) after training and 303 DMRs after the detraining period, which were, in both conditions, enriched at close vicinity of transcription start sites. Ontology analysis of genes located at proximity of DMRs returned terms related to neurological function at the trained state and, to a much lesser extent, at the detrained state. Our study reveal that short-term endurance training induces marked remodeling of the sperm epigenome, and identify genes related to the development of the central nervous system as potential hot spots for epigenetic variation upon environmental stress. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-018-0446-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-25 /pmc/articles/PMC5785820/ /pubmed/29416570 http://dx.doi.org/10.1186/s13148-018-0446-7 Text en © The Author(s). 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 Short Report
Ingerslev, Lars R.
Donkin, Ida
Fabre, Odile
Versteyhe, Soetkin
Mechta, Mie
Pattamaprapanont, Pattarawan
Mortensen, Brynjulf
Krarup, Nikolaj Thure
Barrès, Romain
Endurance training remodels sperm-borne small RNA expression and methylation at neurological gene hotspots
title Endurance training remodels sperm-borne small RNA expression and methylation at neurological gene hotspots
title_full Endurance training remodels sperm-borne small RNA expression and methylation at neurological gene hotspots
title_fullStr Endurance training remodels sperm-borne small RNA expression and methylation at neurological gene hotspots
title_full_unstemmed Endurance training remodels sperm-borne small RNA expression and methylation at neurological gene hotspots
title_short Endurance training remodels sperm-borne small RNA expression and methylation at neurological gene hotspots
title_sort endurance training remodels sperm-borne small rna expression and methylation at neurological gene hotspots
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785820/
https://www.ncbi.nlm.nih.gov/pubmed/29416570
http://dx.doi.org/10.1186/s13148-018-0446-7
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