Cargando…

Epigenetic changes induced by in utero dietary challenge result in phenotypic variability in successive generations of mice

Transmission of epigenetic information between generations occurs in nematodes, flies and plants, mediated by specialised small RNA pathways, modified histones and DNA methylation. Similar processes in mammals can also affect phenotype through intergenerational or trans-generational mechanisms. Here...

Descripción completa

Detalles Bibliográficos
Autores principales: Van de Pette, Mathew, Dimond, Andrew, Galvão, António M., Millership, Steven J., To, Wilson, Prodani, Chiara, McNamara, Gráinne, Bruno, Ludovica, Sardini, Alessandro, Webster, Zoe, McGinty, James, French, Paul M. W., Uren, Anthony G., Castillo-Fernandez, Juan, Watkinson, William, Ferguson-Smith, Anne C., Merkenschlager, Matthias, John, Rosalind M., Kelsey, Gavin, Fisher, Amanda G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072353/
https://www.ncbi.nlm.nih.gov/pubmed/35513363
http://dx.doi.org/10.1038/s41467-022-30022-2
_version_ 1784701041925685248
author Van de Pette, Mathew
Dimond, Andrew
Galvão, António M.
Millership, Steven J.
To, Wilson
Prodani, Chiara
McNamara, Gráinne
Bruno, Ludovica
Sardini, Alessandro
Webster, Zoe
McGinty, James
French, Paul M. W.
Uren, Anthony G.
Castillo-Fernandez, Juan
Watkinson, William
Ferguson-Smith, Anne C.
Merkenschlager, Matthias
John, Rosalind M.
Kelsey, Gavin
Fisher, Amanda G.
author_facet Van de Pette, Mathew
Dimond, Andrew
Galvão, António M.
Millership, Steven J.
To, Wilson
Prodani, Chiara
McNamara, Gráinne
Bruno, Ludovica
Sardini, Alessandro
Webster, Zoe
McGinty, James
French, Paul M. W.
Uren, Anthony G.
Castillo-Fernandez, Juan
Watkinson, William
Ferguson-Smith, Anne C.
Merkenschlager, Matthias
John, Rosalind M.
Kelsey, Gavin
Fisher, Amanda G.
author_sort Van de Pette, Mathew
collection PubMed
description Transmission of epigenetic information between generations occurs in nematodes, flies and plants, mediated by specialised small RNA pathways, modified histones and DNA methylation. Similar processes in mammals can also affect phenotype through intergenerational or trans-generational mechanisms. Here we generate a luciferase knock-in reporter mouse for the imprinted Dlk1 locus to visualise and track epigenetic fidelity across generations. Exposure to high-fat diet in pregnancy provokes sustained re-expression of the normally silent maternal Dlk1 in offspring (loss of imprinting) and increased DNA methylation at the somatic differentially methylated region (sDMR). In the next generation heterogeneous Dlk1 mis-expression is seen exclusively among animals born to F1-exposed females. Oocytes from these females show altered gene and microRNA expression without changes in DNA methylation, and correct imprinting is restored in subsequent generations. Our results illustrate how diet impacts the foetal epigenome, disturbing canonical and non-canonical imprinting mechanisms to modulate the properties of successive generations of offspring.
format Online
Article
Text
id pubmed-9072353
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-90723532022-05-07 Epigenetic changes induced by in utero dietary challenge result in phenotypic variability in successive generations of mice Van de Pette, Mathew Dimond, Andrew Galvão, António M. Millership, Steven J. To, Wilson Prodani, Chiara McNamara, Gráinne Bruno, Ludovica Sardini, Alessandro Webster, Zoe McGinty, James French, Paul M. W. Uren, Anthony G. Castillo-Fernandez, Juan Watkinson, William Ferguson-Smith, Anne C. Merkenschlager, Matthias John, Rosalind M. Kelsey, Gavin Fisher, Amanda G. Nat Commun Article Transmission of epigenetic information between generations occurs in nematodes, flies and plants, mediated by specialised small RNA pathways, modified histones and DNA methylation. Similar processes in mammals can also affect phenotype through intergenerational or trans-generational mechanisms. Here we generate a luciferase knock-in reporter mouse for the imprinted Dlk1 locus to visualise and track epigenetic fidelity across generations. Exposure to high-fat diet in pregnancy provokes sustained re-expression of the normally silent maternal Dlk1 in offspring (loss of imprinting) and increased DNA methylation at the somatic differentially methylated region (sDMR). In the next generation heterogeneous Dlk1 mis-expression is seen exclusively among animals born to F1-exposed females. Oocytes from these females show altered gene and microRNA expression without changes in DNA methylation, and correct imprinting is restored in subsequent generations. Our results illustrate how diet impacts the foetal epigenome, disturbing canonical and non-canonical imprinting mechanisms to modulate the properties of successive generations of offspring. Nature Publishing Group UK 2022-05-05 /pmc/articles/PMC9072353/ /pubmed/35513363 http://dx.doi.org/10.1038/s41467-022-30022-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Van de Pette, Mathew
Dimond, Andrew
Galvão, António M.
Millership, Steven J.
To, Wilson
Prodani, Chiara
McNamara, Gráinne
Bruno, Ludovica
Sardini, Alessandro
Webster, Zoe
McGinty, James
French, Paul M. W.
Uren, Anthony G.
Castillo-Fernandez, Juan
Watkinson, William
Ferguson-Smith, Anne C.
Merkenschlager, Matthias
John, Rosalind M.
Kelsey, Gavin
Fisher, Amanda G.
Epigenetic changes induced by in utero dietary challenge result in phenotypic variability in successive generations of mice
title Epigenetic changes induced by in utero dietary challenge result in phenotypic variability in successive generations of mice
title_full Epigenetic changes induced by in utero dietary challenge result in phenotypic variability in successive generations of mice
title_fullStr Epigenetic changes induced by in utero dietary challenge result in phenotypic variability in successive generations of mice
title_full_unstemmed Epigenetic changes induced by in utero dietary challenge result in phenotypic variability in successive generations of mice
title_short Epigenetic changes induced by in utero dietary challenge result in phenotypic variability in successive generations of mice
title_sort epigenetic changes induced by in utero dietary challenge result in phenotypic variability in successive generations of mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072353/
https://www.ncbi.nlm.nih.gov/pubmed/35513363
http://dx.doi.org/10.1038/s41467-022-30022-2
work_keys_str_mv AT vandepettemathew epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT dimondandrew epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT galvaoantoniom epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT millershipstevenj epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT towilson epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT prodanichiara epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT mcnamaragrainne epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT brunoludovica epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT sardinialessandro epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT websterzoe epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT mcgintyjames epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT frenchpaulmw epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT urenanthonyg epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT castillofernandezjuan epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT watkinsonwilliam epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT fergusonsmithannec epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT merkenschlagermatthias epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT johnrosalindm epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT kelseygavin epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice
AT fisheramandag epigeneticchangesinducedbyinuterodietarychallengeresultinphenotypicvariabilityinsuccessivegenerationsofmice