Methylation status of VTRNA2-1/nc886 is stable across populations, monozygotic twin pairs and in majority of tissues

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.contributor.organizationfi=InFLAMES Lippulaiva|en=InFLAMES Flagship|
dc.contributor.organizationfi=sydäntutkimuskeskus|en=Cardiovascular Medicine (CAPC)|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organizationfi=väestötutkimuskeskus|en=Centre for Population Health Research (POP Centre)|
dc.contributor.organization-code1.2.246.10.2458963.20.35734063924
dc.contributor.organization-code1.2.246.10.2458963.20.42471027641
dc.contributor.organization-code1.2.246.10.2458963.20.68445910604
dc.converis.publication-id176894046
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/176894046
dc.date.accessioned2025-08-27T22:19:08Z
dc.date.available2025-08-27T22:19:08Z
dc.description.abstract<p>Aims & 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. <br></p><p>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 similar to 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. <br></p><p>Conclusion: The nc886 imprint may be established in the oocyte, and, after implantation, the methylation status is stable, excluding a few specific tissues.Tweetable abstract Methylation status of a polymorphically imprinted gene, VTRNA2-1/nc886, is stable in human populations (48 cohorts, n > 30,000) and in somatic tissues, except in cerebellum and skeletal muscle. Twin data suggest it may already be established in the oocyte.</p>
dc.format.pagerange1105
dc.format.pagerange1124
dc.identifier.jour-issn1750-1911
dc.identifier.olddbid201968
dc.identifier.oldhandle10024/184995
dc.identifier.urihttps://www.utupub.fi/handle/11111/38876
dc.identifier.urlhttps://doi.org/10.2217/epi-2022-0228
dc.identifier.urnURN:NBN:fi-fe2022112967791
dc.language.isoen
dc.okm.affiliatedauthorRaitakari, Olli
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherFUTURE MEDICINE LTD
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.2217/epi-2022-0228
dc.relation.ispartofjournalEpigenomics
dc.relation.issue18
dc.relation.volume14
dc.source.identifierhttps://www.utupub.fi/handle/10024/184995
dc.titleMethylation status of VTRNA2-1/nc886 is stable across populations, monozygotic twin pairs and in majority of tissues
dc.year.issued2022

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