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IRS1 DNA promoter methylation and expression in human adipose tissue are related to fat distribution and metabolic traits.
- Source :
-
Scientific reports [Sci Rep] 2017 Sep 28; Vol. 7 (1), pp. 12369. Date of Electronic Publication: 2017 Sep 28. - Publication Year :
- 2017
-
Abstract
- The SNP variant rs2943650 near IRS1 gene locus was previously associated with decreased body fat and IRS1 gene expression as well as an adverse metabolic profile in humans. Here, we hypothesize that these effects may be mediated by an interplay with epigenetic alterations. We measured IRS1 promoter DNA methylation and mRNA expression in paired human subcutaneous and omental visceral adipose tissue samples (SAT and OVAT) from 146 and 41 individuals, respectively. Genotyping of rs2943650 was performed in all individuals (N = 146). We observed a significantly higher IRS1 promoter DNA methylation in OVAT compared to SAT (N = 146, P = 8.0 × 10 <superscript>-6</superscript> ), while expression levels show the opposite effect direction (N = 41, P = 0.011). OVAT and SAT methylation correlated negatively with IRS1 gene expression in obese subjects (N = 16, P = 0.007 and P = 0.010). The major T-allele is related to increased DNA methylation in OVAT (N = 146, P = 0.019). Finally, DNA methylation and gene expression in OVAT correlated with anthropometric traits (waist- circumference waist-to-hip ratio) and parameters of glucose metabolism in obese individuals. Our data suggest that the association between rs2943650 near the IRS1 gene locus with clinically relevant variables may at least be modulated by changes in DNA methylation that translates into altered IRS1 gene expression.
- Subjects :
- Adult
Aged
Body Mass Index
Female
Humans
Insulin Receptor Substrate Proteins metabolism
Male
Middle Aged
Obesity genetics
Obesity metabolism
Polymorphism, Single Nucleotide
Waist-Hip Ratio
Adipose Tissue metabolism
Body Fat Distribution
DNA Methylation
Gene Expression Regulation
Insulin Receptor Substrate Proteins genetics
Promoter Regions, Genetic genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 7
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 28959056
- Full Text :
- https://doi.org/10.1038/s41598-017-12393-5