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dc.contributor.authorMarttila, Saara
dc.contributor.authorTamminen, Hely
dc.contributor.authorRajić, Sonja
dc.contributor.authorMishra, Pashupati P
dc.contributor.authorLehtimäki, Terho
dc.contributor.authorRaitakari, Olli
dc.contributor.authorKähönen, Mika
dc.contributor.authorKananen, Laura
dc.contributor.authorJylhävä, Juulia
dc.contributor.authorHägg, Sara
dc.contributor.authorDelerue, Thomas
dc.contributor.authorPeters, Annette
dc.contributor.authorWaldenberger, Melanie
dc.contributor.authorKleber, Marcus E.
dc.contributor.authorMärz, Winfried
dc.contributor.authorLuoto, Riitta
dc.contributor.authorRaitanen, Jani
dc.contributor.authorSillanpää, Elina
dc.contributor.authorLaakkonen, Eija K.
dc.contributor.authorHeikkinen, Aino
dc.contributor.authorOllikainen, Miina
dc.contributor.authorRaitoharju, Emma
dc.date.accessioned2022-10-18T07:45:26Z
dc.date.available2022-10-18T07:45:26Z
dc.date.issued2022
dc.identifier.citationMarttila, S., Tamminen, H., Rajić, S., Mishra, P. P., Lehtimäki, T., Raitakari, O., Kähönen, M., Kananen, L., Jylhävä, J., Hägg, S., Delerue, T., Peters, A., Waldenberger, M., Kleber, M. E., März, W., Luoto, R., Raitanen, J., Sillanpää, E., Laakkonen, E. K., . . . Raitoharju, E. (2022). Methylation status of VTRNA2-1/nc886 is stable across populations, monozygotic twin pairs and in majority of tissues. <i>Epigenomics</i>, <i>14</i>(18), 1105-1124. <a href="https://doi.org/10.2217/epi-2022-0228" target="_blank">https://doi.org/10.2217/epi-2022-0228</a>
dc.identifier.otherCONVID_157003327
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/83586
dc.description.abstractAims & methods: The aim of this study was to characterize the methylation level of a polymorphically imprinted gene, VTRNA2-1/nc886, in human populations and somatic tissues.48 datasets, consisting of more than 30 tissues and >30,000 individuals, were used. Results:nc886 methylation status is associated with twin status and ethnic background, but the variation between populations is limited. Monozygotic twin pairs present concordant methylation, whereas ∼30% of dizygotic twin pairs present discordant methylation in the nc886 locus. The methylation levels of nc886 are uniform across somatic tissues, except in cerebellum and skeletal muscle. Conclusion: The nc886 imprint may be established in the oocyte, and, after implantation, the methylation status is stable, excluding a few specific tissues.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherFuture Medicine
dc.relation.ispartofseriesEpigenomics
dc.rightsCC BY-NC-ND 4.0
dc.subject.otherdevelopmental origins of health and disease hypothesis
dc.subject.otherDNA methylation
dc.subject.otherimprinting
dc.subject.othermetastable epiallele
dc.subject.otherpolymorphic imprinting
dc.subject.otherpopulation studies
dc.titleMethylation status of VTRNA2-1/nc886 is stable across populations, monozygotic twin pairs and in majority of tissues
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202210184906
dc.contributor.laitosLiikuntatieteellinen tiedekuntafi
dc.contributor.laitosFaculty of Sport and Health Sciencesen
dc.contributor.oppiaineGerontologia ja kansanterveysfi
dc.contributor.oppiaineGerontology and Public Healthen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange1105-1124
dc.relation.issn1750-1911
dc.relation.numberinseries18
dc.relation.volume14
dc.type.versionpublishedVersion
dc.rights.copyright© 2022 The authors
dc.rights.accesslevelopenAccessfi
dc.subject.ysoDNA-metylaatio
dc.subject.ysoväestötutkimus
dc.subject.ysogeeniekspressio
dc.subject.ysogeenit
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p38350
jyx.subject.urihttp://www.yso.fi/onto/yso/p11417
jyx.subject.urihttp://www.yso.fi/onto/yso/p25831
jyx.subject.urihttp://www.yso.fi/onto/yso/p147
dc.rights.urlhttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.relation.doi10.2217/epi-2022-0228
dc.type.okmA1


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