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Impact of the gut microbiota on the m(6)A epitranscriptome of mouse cecum and liver

The intestinal microbiota modulates host physiology and gene expression via mechanisms that are not fully understood. Here we examine whether host epitranscriptomic marks are affected by the gut microbiota. We use methylated RNA-immunoprecipitation and sequencing (MeRIP-seq) to identify N6-methylade...

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Autores principales: Jabs, Sabrina, Biton, Anne, Bécavin, Christophe, Nahori, Marie-Anne, Ghozlane, Amine, Pagliuso, Alessandro, Spanò, Giulia, Guérineau, Vincent, Touboul, David, Giai Gianetto, Quentin, Chaze, Thibault, Matondo, Mariette, Dillies, Marie-Agnès, Cossart, Pascale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067863/
https://www.ncbi.nlm.nih.gov/pubmed/32165618
http://dx.doi.org/10.1038/s41467-020-15126-x
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author Jabs, Sabrina
Biton, Anne
Bécavin, Christophe
Nahori, Marie-Anne
Ghozlane, Amine
Pagliuso, Alessandro
Spanò, Giulia
Guérineau, Vincent
Touboul, David
Giai Gianetto, Quentin
Chaze, Thibault
Matondo, Mariette
Dillies, Marie-Agnès
Cossart, Pascale
author_facet Jabs, Sabrina
Biton, Anne
Bécavin, Christophe
Nahori, Marie-Anne
Ghozlane, Amine
Pagliuso, Alessandro
Spanò, Giulia
Guérineau, Vincent
Touboul, David
Giai Gianetto, Quentin
Chaze, Thibault
Matondo, Mariette
Dillies, Marie-Agnès
Cossart, Pascale
author_sort Jabs, Sabrina
collection PubMed
description The intestinal microbiota modulates host physiology and gene expression via mechanisms that are not fully understood. Here we examine whether host epitranscriptomic marks are affected by the gut microbiota. We use methylated RNA-immunoprecipitation and sequencing (MeRIP-seq) to identify N6-methyladenosine (m(6)A) modifications in mRNA of mice carrying conventional, modified, or no microbiota. We find that variations in the gut microbiota correlate with m(6)A modifications in the cecum, and to a lesser extent in the liver, affecting pathways related to metabolism, inflammation and antimicrobial responses. We analyze expression levels of several known writer and eraser enzymes, and find that the methyltransferase Mettl16 is downregulated in absence of a microbiota, and one of its target mRNAs, encoding S-adenosylmethionine synthase Mat2a, is less methylated. We furthermore show that Akkermansia muciniphila and Lactobacillus plantarum affect specific m(6)A modifications in mono-associated mice. Our results highlight epitranscriptomic modifications as an additional level of interaction between commensal bacteria and their host.
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spelling pubmed-70678632020-03-18 Impact of the gut microbiota on the m(6)A epitranscriptome of mouse cecum and liver Jabs, Sabrina Biton, Anne Bécavin, Christophe Nahori, Marie-Anne Ghozlane, Amine Pagliuso, Alessandro Spanò, Giulia Guérineau, Vincent Touboul, David Giai Gianetto, Quentin Chaze, Thibault Matondo, Mariette Dillies, Marie-Agnès Cossart, Pascale Nat Commun Article The intestinal microbiota modulates host physiology and gene expression via mechanisms that are not fully understood. Here we examine whether host epitranscriptomic marks are affected by the gut microbiota. We use methylated RNA-immunoprecipitation and sequencing (MeRIP-seq) to identify N6-methyladenosine (m(6)A) modifications in mRNA of mice carrying conventional, modified, or no microbiota. We find that variations in the gut microbiota correlate with m(6)A modifications in the cecum, and to a lesser extent in the liver, affecting pathways related to metabolism, inflammation and antimicrobial responses. We analyze expression levels of several known writer and eraser enzymes, and find that the methyltransferase Mettl16 is downregulated in absence of a microbiota, and one of its target mRNAs, encoding S-adenosylmethionine synthase Mat2a, is less methylated. We furthermore show that Akkermansia muciniphila and Lactobacillus plantarum affect specific m(6)A modifications in mono-associated mice. Our results highlight epitranscriptomic modifications as an additional level of interaction between commensal bacteria and their host. Nature Publishing Group UK 2020-03-12 /pmc/articles/PMC7067863/ /pubmed/32165618 http://dx.doi.org/10.1038/s41467-020-15126-x Text en © The Author(s) 2020 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
Jabs, Sabrina
Biton, Anne
Bécavin, Christophe
Nahori, Marie-Anne
Ghozlane, Amine
Pagliuso, Alessandro
Spanò, Giulia
Guérineau, Vincent
Touboul, David
Giai Gianetto, Quentin
Chaze, Thibault
Matondo, Mariette
Dillies, Marie-Agnès
Cossart, Pascale
Impact of the gut microbiota on the m(6)A epitranscriptome of mouse cecum and liver
title Impact of the gut microbiota on the m(6)A epitranscriptome of mouse cecum and liver
title_full Impact of the gut microbiota on the m(6)A epitranscriptome of mouse cecum and liver
title_fullStr Impact of the gut microbiota on the m(6)A epitranscriptome of mouse cecum and liver
title_full_unstemmed Impact of the gut microbiota on the m(6)A epitranscriptome of mouse cecum and liver
title_short Impact of the gut microbiota on the m(6)A epitranscriptome of mouse cecum and liver
title_sort impact of the gut microbiota on the m(6)a epitranscriptome of mouse cecum and liver
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067863/
https://www.ncbi.nlm.nih.gov/pubmed/32165618
http://dx.doi.org/10.1038/s41467-020-15126-x
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