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

Lehtimäki Terho; Matias‑Garcia Pamela R.; Kähönen Mika; Viiri Leena E.; Mononen Nina; Mishra Pashupati P.; Aalto‑Setälä Katriina; Marttila Saara; Winkelmann Juliane; Hutri‑Kähönen Nina; Peters Annette; Rathmann Wolfgang; Raitoharju Emma; Raitakari Olli; Waldenberger Melanie; Ceder Tiina; Juonala Markus; Lyytikäinen Leo‑Pekka; Kühnel Brigitte

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

Lehtimäki Terho
Matias‑Garcia Pamela R.
Kähönen Mika
Viiri Leena E.
Mononen Nina
Mishra Pashupati P.
Aalto‑Setälä Katriina
Marttila Saara
Winkelmann Juliane
Hutri‑Kähönen Nina
Peters Annette
Rathmann Wolfgang
Raitoharju Emma
Raitakari Olli
Waldenberger Melanie
Ceder Tiina
Juonala Markus
Lyytikäinen Leo‑Pekka
Kühnel Brigitte
Katso/Avaa
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BMC
doi:10.1186/s13148-021-01132-3
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021093049094
Tiivistelmä

Background

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.

Results

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.

Conclusions

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.

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