Insulin and Glucose Alter Death-Associated Protein Kinase 3 (DAPK3) DNA Methylation in Human Skeletal Muscle

Research output: Contribution to journalJournal articleResearchpeer-review

  • Jonathan M Mudry
  • David G Lassiter
  • Carolina Nylén
  • Sonia García-Calzón
  • Erik Näslund
  • Anna Krook
  • Zierath, Juleen R

DNA methylation is altered by environmental factors. We hypothesized DNA methylation is altered in skeletal muscle in response to either insulin or glucose exposure. We performed a genome-wide DNA methylation analysis in muscle from healthy men before and after insulin exposure. DNA methylation of selected genes was determined in muscle from healthy and type 2 diabetic men before and after a glucose tolerance test. Insulin altered DNA methylation in the 3'UTR of the calcium pump ATP2A3 gene. Insulin increased DNA methylation in the gene body of DAPK3, a gene involved in cell proliferation, apoptosis and autophagy. DAPK3 methylation was reduced in type 2 diabetic patients. Carbohydrate ingestion reduced DAPK3 DNA methylation in healthy and type 2 diabetic men, suggesting glucose may play a role. Supporting this, DAPK3 DNA methylation was inversely correlated with the 2 hr glucose concentration. While glucose incorporation to glycogen was unaltered by siRNA against DAPK3, palmitate oxidation was increased. In conclusion, insulin and glucose exposure acutely alter the DNA methylation profile of skeletal muscle, indicating DNA methylation constitutes a rapidly and adaptive epigenetic mark. Furthermore, insulin and glucose modulate DAPK3 DNA methylation in a reciprocal manner suggesting a feedback loop in the control of the epigenome.

Original languageEnglish
JournalDiabetes
Volume66
Issue number3
Pages (from-to)651-662
ISSN0012-1797
DOIs
Publication statusPublished - Mar 2017

ID: 172431977