» Articles » PMID: 34294131

Methylation Status of Nc886 Epiallele Reflects Periconceptional Conditions and is Associated with Glucose Metabolism Through Nc886 RNAs

Abstract

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.

Citing Articles

Commentary on "Epigenome-wide analysis across the development span of pediatric acute lymphoblastic leukemia: backtracking to birth".

Raitoharju E, Marttila S Mol Cancer. 2025; 24(1):8.

PMID: 39799337 PMC: 11724579. DOI: 10.1186/s12943-024-02220-7.


The mystique of epigenetic regulation: the remarkable case of a human noncoding RNA, nc886.

Lee Y, Lee Y Epigenomics. 2024; 16(21-22):1389-1405.

PMID: 39466123 PMC: 11728332. DOI: 10.1080/17501911.2024.2415278.


Early resilience and epigenetic ageing: Results from the prospective Young Finns Study with a 31-year follow-up.

Aino S, Saarinen A, Saara M, Marttila S, Mishra Pashupati P, Mishra P Aging Cell. 2024; 24(2):e14394.

PMID: 39460379 PMC: 11822653. DOI: 10.1111/acel.14394.


Epigenetics of the non-coding RNA nc886 across blood, adipose tissue and skeletal muscle in offspring exposed to diabetes in pregnancy.

Hjort L, Bredgaard S, Manitta E, Marques I, Sorensen A, Martino D Clin Epigenetics. 2024; 16(1):61.

PMID: 38715048 PMC: 11077860. DOI: 10.1186/s13148-024-01673-3.


Non-coding 886 (/), the epigenetic odd duck - implications for future studies.

Raitoharju E, Rajic S, Marttila S Epigenetics. 2024; 19(1):2332819.

PMID: 38525792 PMC: 10965113. DOI: 10.1080/15592294.2024.2332819.


References
1.
Kong L, Hao Q, Wang Y, Zhou P, Zou B, Zhang Y . Regulation of p53 expression and apoptosis by vault RNA2-1-5p in cervical cancer cells. Oncotarget. 2015; 6(29):28371-88. PMC: 4695066. DOI: 10.18632/oncotarget.4948. View

2.
Moore T, Haig D . Genomic imprinting in mammalian development: a parental tug-of-war. Trends Genet. 1991; 7(2):45-9. DOI: 10.1016/0168-9525(91)90230-N. View

3.
Elovainio M, Taipale T, Seppala I, Mononen N, Raitoharju E, Jokela M . Activated immune-inflammatory pathways are associated with long-standing depressive symptoms: Evidence from gene-set enrichment analyses in the Young Finns Study. J Psychiatr Res. 2015; 71:120-5. DOI: 10.1016/j.jpsychires.2015.09.017. View

4.
Carpenter B, Zhou W, Madaj Z, DeWitt A, Ross J, Gronbaek K . Mother-child transmission of epigenetic information by tunable polymorphic imprinting. Proc Natl Acad Sci U S A. 2018; 115(51):E11970-E11977. PMC: 6304996. DOI: 10.1073/pnas.1815005115. View

5.
Hu Z, Zhang H, Tang L, Lou M, Geng Y . Silencing nc886, a Non-Coding RNA, Induces Apoptosis of Human Endometrial Cancer Cells-1A In Vitro. Med Sci Monit. 2017; 23:1317-1324. PMC: 5365049. DOI: 10.12659/msm.900320. View