dc.contributor.author | Marttila, Saara | |
dc.contributor.author | Tamminen, Hely | |
dc.contributor.author | Rajić, Sonja | |
dc.contributor.author | Mishra, Pashupati P | |
dc.contributor.author | Lehtimäki, Terho | |
dc.contributor.author | Raitakari, Olli | |
dc.contributor.author | Kähönen, Mika | |
dc.contributor.author | Kananen, Laura | |
dc.contributor.author | Jylhävä, Juulia | |
dc.contributor.author | Hägg, Sara | |
dc.contributor.author | Delerue, Thomas | |
dc.contributor.author | Peters, Annette | |
dc.contributor.author | Waldenberger, Melanie | |
dc.contributor.author | Kleber, Marcus E. | |
dc.contributor.author | März, Winfried | |
dc.contributor.author | Luoto, Riitta | |
dc.contributor.author | Raitanen, Jani | |
dc.contributor.author | Sillanpää, Elina | |
dc.contributor.author | Laakkonen, Eija K. | |
dc.contributor.author | Heikkinen, Aino | |
dc.contributor.author | Ollikainen, Miina | |
dc.contributor.author | Raitoharju, Emma | |
dc.date.accessioned | 2022-10-18T07:45:26Z | |
dc.date.available | 2022-10-18T07:45:26Z | |
dc.date.issued | 2022 | |
dc.identifier.citation | Marttila, 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.other | CONVID_157003327 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/83586 | |
dc.description.abstract | 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.
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.mimetype | application/pdf | |
dc.language.iso | eng | |
dc.publisher | Future Medicine | |
dc.relation.ispartofseries | Epigenomics | |
dc.rights | CC BY-NC-ND 4.0 | |
dc.subject.other | developmental origins of health and disease hypothesis | |
dc.subject.other | DNA methylation | |
dc.subject.other | imprinting | |
dc.subject.other | metastable epiallele | |
dc.subject.other | polymorphic imprinting | |
dc.subject.other | population studies | |
dc.title | Methylation status of VTRNA2-1/nc886 is stable across populations, monozygotic twin pairs and in majority of tissues | |
dc.type | article | |
dc.identifier.urn | URN:NBN:fi:jyu-202210184906 | |
dc.contributor.laitos | Liikuntatieteellinen tiedekunta | fi |
dc.contributor.laitos | Faculty of Sport and Health Sciences | en |
dc.contributor.oppiaine | Gerontologia ja kansanterveys | fi |
dc.contributor.oppiaine | Gerontology and Public Health | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.format.pagerange | 1105-1124 | |
dc.relation.issn | 1750-1911 | |
dc.relation.numberinseries | 18 | |
dc.relation.volume | 14 | |
dc.type.version | publishedVersion | |
dc.rights.copyright | © 2022 The authors | |
dc.rights.accesslevel | openAccess | fi |
dc.subject.yso | DNA-metylaatio | |
dc.subject.yso | väestötutkimus | |
dc.subject.yso | geeniekspressio | |
dc.subject.yso | geenit | |
dc.format.content | fulltext | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p38350 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p11417 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p25831 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p147 | |
dc.rights.url | https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.relation.doi | 10.2217/epi-2022-0228 | |
dc.type.okm | A1 | |