Methylation status of nc886 epiallele reflects periconceptional conditions and is associated with glucose metabolism through nc886 RNAs

dc.contributor.authorMarttila Saara
dc.contributor.authorViiri Leena E.
dc.contributor.authorMishra Pashupati P.
dc.contributor.authorKühnel Brigitte
dc.contributor.authorMatias‑Garcia Pamela R.
dc.contributor.authorLyytikäinen Leo‑Pekka
dc.contributor.authorCeder Tiina
dc.contributor.authorMononen Nina
dc.contributor.authorRathmann Wolfgang
dc.contributor.authorWinkelmann Juliane
dc.contributor.authorPeters Annette
dc.contributor.authorKähönen Mika
dc.contributor.authorHutri‑Kähönen Nina
dc.contributor.authorJuonala Markus
dc.contributor.authorAalto‑Setälä Katriina
dc.contributor.authorRaitakari Olli
dc.contributor.authorLehtimäki Terho
dc.contributor.authorWaldenberger Melanie
dc.contributor.authorRaitoharju Emma
dc.contributor.organizationfi=InFLAMES Lippulaiva|en=InFLAMES Flagship|
dc.contributor.organizationfi=sisätautioppi|en=Internal Medicine|
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-code1.2.246.10.2458963.20.40502528769
dc.contributor.organization-code1.2.246.10.2458963.20.42471027641
dc.contributor.organization-code1.2.246.10.2458963.20.68445910604
dc.converis.publication-id66942732
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/66942732
dc.date.accessioned2022-10-28T14:28:55Z
dc.date.available2022-10-28T14:28:55Z
dc.description.abstract<p>Background</p><p>Non-coding RNA 886 (nc886) is coded from a maternally inherited metastable epiallele. We set out to investigate the determinants and dynamics of the methylation pattern at the nc886 epiallele and how this methylation status associates with nc886 RNA expression. Furthermore, we investigated the associations between the nc886 methylation status or the levels of nc886 RNAs and metabolic traits in the YFS and KORA cohorts. The association between nc886 epiallele methylation and RNA expression was also validated in induced pluripotent stem cell (iPSC) lines.</p><p>Results</p><p>We confirm that the methylation status of the nc886 epiallele is mostly binomial, with individuals displaying either a non- or hemi-methylated status, but we also describe intermediately and close to fully methylated individuals. We show that an individual's methylation status is associated with the mother's age and socioeconomic status, but not with the individual's own genetics. Once established, the methylation status of the nc886 epiallele remains stable for at least 25 years. This methylation status is strongly associated with the levels of nc886 non-coding RNAs in serum, blood, and iPSC lines. In addition, nc886 methylation status associates with glucose and insulin levels during adolescence but not with the indicators of glucose metabolism or the incidence of type 2 diabetes in adulthood. However, the nc886-3p RNA levels also associate with glucose metabolism in adulthood.</p><p>Conclusions</p><p>These results indicate that nc886 metastable epiallele methylation is tuned by the periconceptional conditions and it associates with glucose metabolism through the expression of the ncRNAs coded in the epiallele region.</p>
dc.identifier.eissn1868-7083
dc.identifier.jour-issn1868-7075
dc.identifier.olddbid188526
dc.identifier.oldhandle10024/171620
dc.identifier.urihttps://www.utupub.fi/handle/11111/53406
dc.identifier.urnURN:NBN:fi-fe2021093049094
dc.language.isoen
dc.okm.affiliatedauthorJuonala, Markus
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.publisherBMC
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumberARTN 143
dc.relation.doi10.1186/s13148-021-01132-3
dc.relation.ispartofjournalClinical Epigenetics
dc.relation.issue1
dc.relation.volume13
dc.source.identifierhttps://www.utupub.fi/handle/10024/171620
dc.titleMethylation status of nc886 epiallele reflects periconceptional conditions and is associated with glucose metabolism through nc886 RNAs
dc.year.issued2021

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