Environmentally sensitive hotspots in the methylome of the early human embryo

dc.contributor.authorSilver, Matt J.
dc.contributor.authorSaffari, Ayden
dc.contributor.authorKessler, Noah J.
dc.contributor.authorChandak, Gririraj R.
dc.contributor.authorFall, Caroline H. D.
dc.contributor.authorIssarapu, Prachand
dc.contributor.authorDedaniya, Akshay
dc.contributor.authorBetts, Modupeh
dc.contributor.authorMoore, Sophie E.
dc.contributor.authorRoutledge, Michael N.
dc.contributor.authorHerceg, Zdenko
dc.contributor.authorCuenin, Cyrille
dc.contributor.authorDerakhshan, Maria
dc.contributor.authorJames, Philip T.
dc.contributor.authorMonk, David
dc.contributor.authorPrentice, Andrew M.
dc.date.accessioned2022-04-07T10:45:44Z
dc.date.available2022-04-07T10:45:44Z
dc.date.issued2022-01-06
dc.date.updated2022-04-07T09:52:13Z
dc.description.abstractIn humans, DNA methylation marks inherited from gametes are largely erased following fertilisation, prior to construction of the embryonic methylome. Exploiting a natural experiment of seasonal variation including changes in diet and nutritional status in rural Gambia, we analysed three datasets covering two independent child cohorts and identified 259 CpGs showing consistent associations between season of conception (SoC) and DNA methylation. SoC effects were most apparent in early infancy, with evidence of attenuation by mid-childhood. SoC-associated CpGs were enriched for metastable epialleles, parent-of-origin-specific methylation and germline differentially methylated regions, supporting a periconceptional environmental influence. Many SoC-associated CpGs overlapped enhancers or sites of active transcription in H1 embryonic stem cells and fetal tissues. Half were influenced but not determined by measured genetic variants that were independent of SoC. Environmental 'hotspots' providing a record of environmental influence at periconception constitute a valuable resource for investigating epigenetic mechanisms linking early exposures to lifelong health and disease.ca
dc.format.extent43 p.
dc.format.mimetypeapplication/pdf
dc.identifier.issn2050-084X
dc.identifier.pmid35188105
dc.identifier.urihttps://hdl.handle.net/2445/184813
dc.language.isoengca
dc.publishereLife Sciences Publications, Ltdca
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.7554/eLife.72031.sa2
dc.relation.ispartofeLife, 2022
dc.relation.urihttps://doi.org/10.7554/eLife.72031.sa2
dc.rightscc by (c) Silver, Matt J. et al, 2022
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationMetilació
dc.subject.classificationADN
dc.subject.otherMethylation
dc.subject.otherDNA
dc.titleEnvironmentally sensitive hotspots in the methylome of the early human embryoca
dc.typeinfo:eu-repo/semantics/articleca
dc.typeinfo:eu-repo/semantics/publishedVersion

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