SwePub
Sök i LIBRIS databas

  Utökad sökning

onr:"swepub:oai:lup.lub.lu.se:41a42a5b-fbb0-407c-a795-361e3ae036a0"
 

Sökning: onr:"swepub:oai:lup.lub.lu.se:41a42a5b-fbb0-407c-a795-361e3ae036a0" > DNA methylation and...

  • Main, Ailsa MariaCopenhagen University Hospital (författare)

DNA methylation and gene expression of HIF3A : cross-tissue validation and associations with BMI and insulin resistance

  • Artikel/kapitelEngelska2016

Förlag, utgivningsår, omfång ...

  • 2016-09-02
  • Springer Science and Business Media LLC,2016

Nummerbeteckningar

  • LIBRIS-ID:oai:lup.lub.lu.se:41a42a5b-fbb0-407c-a795-361e3ae036a0
  • https://lup.lub.lu.se/record/41a42a5b-fbb0-407c-a795-361e3ae036a0URI
  • https://doi.org/10.1186/s13148-016-0258-6DOI

Kompletterande språkuppgifter

  • Språk:engelska
  • Sammanfattning på:engelska

Ingår i deldatabas

Klassifikation

  • Ämneskategori:art swepub-publicationtype
  • Ämneskategori:ref swepub-contenttype

Anmärkningar

  • Background: Associations between BMI and DNA methylation of hypoxia-inducible factor 3-alpha (HIF3A) in both blood cells and subcutaneous adipose tissue (SAT) have been reported. In this study, we investigated associations between BMI and HIF3A DNA methylation in the blood and SAT from the same individuals, and whether HIF3A gene expression in SAT and skeletal muscle biopsies showed associations with BMI and insulin resistance. Furthermore, we aimed to investigate gender specificity and heritability of these traits. Methods: We studied 137 first-degree relatives of type 2 diabetes (T2D) patients from 48 families, from whom we had SAT and muscle biopsies. DNA methylation of four CpG sites in the HIF3A promoter was analyzed in the blood and SAT by pyrosequencing, and HIF3A gene expression was analyzed in SAT and muscle by qPCR. An index of whole-body insulin sensitivity was estimated from oral glucose tolerance tests. Results: BMI was associated with HIF3A methylation at one CpG site in the blood, and there was a positive association between the blood and SAT methylation levels at a different CpG site within the individuals. The SAT methylation level did not correlate with HIF3A gene expression. Interestingly, HIF3A expression in SAT, but not in muscle, associated negatively with BMI and whole-body insulin resistance. We found a significant effect of familiality on HIF3A methylation levels in the blood and HIF3A expression levels in skeletal muscle. Conclusions: Our findings are in line with the previously reported link between BMI and DNA methylation of HIF3A in the blood. The tissue-specific results of HIF3A gene expression indicate that SAT is the more functional tissue in which a low expression may adversely affect whole-body insulin sensitivity.

Ämnesord och genrebeteckningar

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Gillberg, LinnCopenhagen University Hospital,University of Copenhagen(Swepub:lu)med-lge (författare)
  • Jacobsen, Anna LouisaCopenhagen University Hospital (författare)
  • Nilsson, EmmaLund University,Lunds universitet,-lup-obsolete,Forskargrupper vid Lunds universitet,LUDC (Lund University Diabetes Centre)-lup-obsolete,Lund University Research Groups,Copenhagen University Hospital(Swepub:lu)geol-eno (författare)
  • Gjesing, Anette PriorUniversity of Copenhagen (författare)
  • Hansen, TorbenUniversity of Copenhagen (författare)
  • Pedersen, OlufUniversity of Copenhagen (författare)
  • Ribel-Madsen, RasmusOdense University Hospital (författare)
  • Vaag, AllanCopenhagen University Hospital(Swepub:lu)med-ava (författare)
  • Copenhagen University HospitalUniversity of Copenhagen (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:Clinical Epigenetics: Springer Science and Business Media LLC8:11868-70751868-7083

Internetlänk

Hitta via bibliotek

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy