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  • Marttila, S (author)

Methylation status of VTRNA2-1/nc886 is stable across populations, monozygotic twin pairs and in majority of tissues

  • Article/chapterEnglish2022

Publisher, publication year, extent ...

  • Future Medicine Ltd,2022

Numbers

  • LIBRIS-ID:oai:prod.swepub.kib.ki.se:150902201
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:150902201URI
  • https://doi.org/10.2217/epi-2022-0228DOI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • 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.

Added entries (persons, corporate bodies, meetings, titles ...)

  • Tamminen, H (author)
  • Rajic, S (author)
  • Mishra, PP (author)
  • Lehtimaki, T (author)
  • Raitakari, O (author)
  • Kahonen, M (author)
  • Kananen, LKarolinska Institutet (author)
  • Jylhava, JKarolinska Institutet (author)
  • Hagg, SKarolinska Institutet (author)
  • Delerue, T (author)
  • Peters, A (author)
  • Waldenberger, M (author)
  • Kleber, ME (author)
  • Marz, W (author)
  • Luoto, R (author)
  • Raitanen, J (author)
  • Sillanpaa, E (author)
  • Laakkonen, EK (author)
  • Heikkinen, A (author)
  • Ollikainen, M (author)
  • Raitoharju, E (author)
  • Karolinska Institutet (creator_code:org_t)

Related titles

  • In:Epigenomics: Future Medicine Ltd14:18, s. 1105-11241750-192X1750-1911

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