Staff overview – University of Copenhagen

Altered DNA methylation of glycolytic and lipogenic genes in liver from obese and type 2 diabetic patients

Research output: Contribution to journalJournal articleResearchpeer-review

Henriette Kirchner, Indranil Sinha, Hui Gao, Maxwell A Ruby, Milena Schönke, Jessica M Lindvall, Romain Barrès, Anna Krook, Erik Näslund, Karin Dahlman-Wright, Juleen R Zierath

OBJECTIVE: Epigenetic modifications contribute to the etiology of type 2 diabetes.

METHOD: We performed genome-wide methylome and transcriptome analysis in liver from severely obese men with or without type 2 diabetes and non-obese men to discover aberrant pathways underlying the development of insulin resistance. Results were validated by pyrosequencing.

RESULT: We identified hypomethylation of genes involved in hepatic glycolysis and insulin resistance, concomitant with increased mRNA expression and protein levels. Pyrosequencing revealed the CpG-site within ATF-motifs was hypomethylated in four of these genes in liver of severely obese non-diabetic and type 2 diabetic patients, suggesting epigenetic regulation of transcription by altered ATF-DNA binding.

CONCLUSION: Severely obese non-diabetic and type 2 diabetic patients have distinct alterations in the hepatic methylome and transcriptome, with hypomethylation of several genes controlling glucose metabolism within the ATF-motif regulatory site. Obesity appears to shift the epigenetic program of the liver towards increased glycolysis and lipogenesis, which may exacerbate the development of insulin resistance.

Original languageEnglish
JournalMolecular Metabolism
Volume5
Issue number3
Pages (from-to)171-83
Number of pages13
ISSN2212-8778
DOIs
StatePublished - Mar 2016

Number of downloads are based on statistics from Google Scholar and www.ku.dk


No data available

ID: 159743545