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DOI 10.3305/nh.2014.30.6.7843

Медицинская библиотека · Nutricion hospitalaria · 2014

Time-specific changes in DNA methyltransferases associated with the leptin promoter during the development of obesity.

Xia Lulu, Wang Cui, Lu Yuanyuan, Fan Chaonan, Ding Xu, Fu Huicong, Qi Kemin

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

The role of epigenetic modifications on leptin expression during the development of obesity has not been clearly determined. This study aimed to investigate changes in the expression of DNA methyltransferases (DNMTs) at the leptin promoter and their effect on gene transcription during the development of obesity.

METHODS

Using a high-fat diet (HFD)-induced obese (DIO) mouse model, we examined adipose expression of leptin, its promoter associated DNMTs and the methyl CpG-binding domain protein 2 (MBD2) at different time points after HFD feeding.

RESULTS

The leptin expression levels in epididymal fat were significantly increased after feeding the mice a HFD for 4, 8, 12 and 18 weeks (w), as opposed to feeding them a standard diet (SD). However, the CpG promoter methylation fractions were significantly reduced at 8 w with a decreased association of MBD2 and DNMT1, and increased at 12 w and 18 w with an increased association of MBD2, DNMT3A and DNMT3B, after HFD feeding. Additionally, the binding of RNA polymerase II was increased at 8 w and decreased at 18 w after HFD feeding compared with SD feeding.

CONCLUSIONS

These data indicate that time-specific changes in promoter associated DNMTs may be associated with the regulation of leptin expression, indicating that a complex and dynamic epigenetic mechanism underlies aberrant leptin expression during the development of obesity.

Для цитирования: Xia Lulu, Wang Cui, Lu Yuanyuan, Fan Chaonan, Ding Xu, Fu Huicong, Qi Kemin. Time-specific changes in DNA methyltransferases associated with the leptin promoter during the development of obesity.. Nutricion hospitalaria. 2014. DOI: 10.3305/nh.2014.30.6.7843.

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