Abstract
Background: Epidemiological evidence indicates yet unknown epigenetic mechanisms underlying a propensity for overweight and type 2 diabetes. We analyzed the extent of methylation at lysine 4 and lysine 9 of histone H3 in primary human adipocytes from 43 subjects using modification-specific antibodies. Results: The level of lysine 9 dimethylation was stable, while adipocytes from type 2 diabetic and non-diabetic overweight subjects exhibited about 40% lower levels of lysine 4 dimethylation compared with cells from normal-weight subjects. In contrast, trimethylation at lysine 4 was 40% higher in adipocytes from overweight diabetic subjects compared with normal-weight and overweight non-diabetic subjects. There was no association between level of modification and age of subjects. Conclusions: The findings define genome-wide molecular modifications of histones in adipocytes that are directly associated with overweight and diabetes, and thus suggest a molecular basis for existing epidemiological evidence of epigenetic inheritance. © 2013 Jufvas et al.; licensee BioMed Central Ltd.
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Jufvas, Å., Sjödin, S., Lundqvist, K., Amin, R., Vener, A. V., & Strålfors, P. (2013). Global differences in specific histone H3 methylation are associated with overweight and type 2 diabetes. Clinical Epigenetics, 5(1). https://doi.org/10.1186/1868-7083-5-15
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