首页> 美国卫生研究院文献>Scientific Reports >Epigenetic Modification of the Leptin Promoter in Diet-Induced Obese Mice and the Effects of N-3 Polyunsaturated Fatty Acids
【2h】

Epigenetic Modification of the Leptin Promoter in Diet-Induced Obese Mice and the Effects of N-3 Polyunsaturated Fatty Acids

机译:瘦素启动子在饮食诱导的肥胖小鼠中的表观遗传修饰和N-3多不饱和脂肪酸的影响

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We report evidence of a detailed epigenetic modification of the leptin promoter and the effects of n-3 polyunsaturated fatty acids (n-3 PUFAs), which is closely associated with the leptin gene transcription in obesity. In the adipose tissue of diet induced obese (DIO) mice, methylation of the CpG island and the binding of methyl-CpG-binding domain protein 2 (MBD2) and DNA methyltransferases (DNMTs) at the leptin promoter are increased and RNA Pol II is decreased. Additionally, histones H3 and H4 are hypoacetylated, lysine 4 of histone H3 (H3K4) is hypomethylated and the binding of histone deacetylases (HDACs) 1, 2 and 6 is increased at the leptin promoter in the DIO mice. These modifications may serve a feedback role to maintain leptin concentrations within a normal range. The regulation of leptin transcriptional expression by n-3 PUFAs is mediated, at least in part, by epigenetic targets, such as MBD2 and histone modifications.
机译:我们报告的瘦素启动子和n-3多不饱和脂肪酸(n-3 PUFAs)的详细表观遗传修饰的证据,这与肥胖中的瘦素基因转录密切相关。在饮食诱发的肥胖(DIO)小鼠的脂肪组织中,瘦素启动子处CpG岛的甲基化以及甲基CpG结合域蛋白2(MBD2)和DNA甲基转移酶(DNMT)的结合增加,RNA Pol II为减少。此外,组蛋白H3和H4被低乙酰化,组蛋白H3(H3K4)的赖氨酸4被低甲基化,在DIO小鼠的瘦素启动子上,组蛋白脱乙酰基酶(HDACs)1、2和6的结合增加。这些修饰可以起到将瘦蛋白浓度维持在正常范围内的反馈作用。 n-3 PUFA对瘦蛋白转录表达的调节至少部分地由表观遗传学靶标(例如MBD2和组蛋白修饰)介导。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号