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...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
---|---|
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 |