Methylation status of VTRNA2-1/nc886 is stable across populations, monozygotic twin pairs and in majority of tissues
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. Epigenomics, 14(18), 1105-1124. https://doi.org/10.2217/epi-2022-0228
Published in
EpigenomicsAuthors
Date
2022Copyright
© 2022 The authors
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.
Publisher
Future MedicineISSN Search the Publication Forum
1750-1911Keywords
Publication in research information system
https://converis.jyu.fi/converis/portal/detail/Publication/157003327
Metadata
Show full item recordCollections
- Liikuntatieteiden tiedekunta [3146]
License
Related items
Showing items with similar title or keywords.
-
DNA methylation links prenatal smoking exposure to later life health outcomes in offspring
Wiklund, Petri; Karhunen, Ville; Richmond, Rebecca C.; Parmar, Priyanka; Rodriguez, Alina; De Silva, Maneka; Wielscher, Matthias; Rezwan, Faisal I.; Richardson, Tom G.; Veijola, Juha; Herzig, Karl-Heinz; Holloway, John W.; Relton, Caroline L.; Sebert, Sylvain; Järvelin, Marjo-Riitta (Biomed Central, 2019)Background: Maternal smoking during pregnancy is associated with adverse offspring health outcomes across their life course. We hypothesize that DNA methylation is a potential mediator of this relationship. Methods: We ... -
From maternal glucocorticoid and thyroid hormones to epigenetic regulation of offspring gene expression : An experimental study in a wild bird species
Hukkanen, Mikaela; Hsu, Bin‐Yan; Cossin‐Sevrin, Nina; Crombecque, Mélanie; Delaunay, Axelle; Hollmen, Lotta; Kaukonen, Riina; Konki, Mikko; Lund, Riikka; Marciau, Coline; Stier, Antoine; Ruuskanen, Suvi (Wiley, 2023)Offspring phenotype at birth is determined by its genotype and the prenatal environment including exposure to maternal hormones. Variation in both maternal glucocorticoids and thyroid hormones can affect offspring phenotype, ... -
Hormone Replacement Therapy Associated White Blood Cell DNA Methylation and Gene Expression are Associated With Within-Pair Differences of Body Adiposity and Bone Mass
Bahl, Aileen; Pöllänen, Eija; Ismail, Khadeeja; Sipilä, Sarianna; Mikkola, Tuija; Berglund, Eva; Lindqvist, Carl Mårten; Syvänen, Ann-Christine; Rantanen, Taina; Kaprio, Jaakko; Kovanen, Vuokko; Ollikainen, Miina (Cambridge University Press; International Society for Twin Studies, 2015)The loss of estrogen during menopause causes changes in the female body, with wide-ranging effects on health. Estrogen-containing hormone replacement therapy (HRT) leads to a relief of typical menopausal symptoms, benefits ... -
Early-life environmental effects on birds : epigenetics and microbiome as mechanisms underlying long-lasting phenotypic changes
Ruuskanen, Suvi (The Company of Biologists, 2024)Although the long-lasting effects of variation in early-life environment have been well documented across organisms, the underlying causal mechanisms are only recently starting to be unraveled. Yet understanding the ... -
DNA methylation changes and somatic mutations as tumorigenic events in Lynch syndrome-associated adenomas retaining mismatch repair protein expression
Mäki-Nevala, Satu; Valo, Satu; Ristimäki, Ari; Sarhadi, Virinder; Knuutila, Sakari; Nyström, Minna; Renkonen-Sinisalo, Laura; Lepistö, Anna; Mecklin, Jukka-Pekka; Peltomäki, Päivi (Elsevier BV, 2019)Background DNA mismatch repair (MMR) defects are a major factor in colorectal tumorigenesis in Lynch syndrome (LS) and 15% of sporadic cases. Some adenomas from carriers of inherited MMR gene mutations have intact MMR ...