Suppr超能文献

饮食诱导肥胖小鼠中瘦素启动子的表观遗传修饰及n-3多不饱和脂肪酸的作用

Epigenetic modification of the leptin promoter in diet-induced obese mice and the effects of N-3 polyunsaturated fatty acids.

作者信息

Shen Wenwen, Wang Cui, Xia Lulu, Fan Chaonan, Dong Hua, Deckelbaum Richard J, Qi Kemin

机构信息

1] Nutrition Research Unit, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, Beijing, China. No. 56 Nan-li-shi Road, Beijing 100045, China [2].

Nutrition Research Unit, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, Beijing, China. No. 56 Nan-li-shi Road, Beijing 100045, China.

出版信息

Sci Rep. 2014 Jun 13;4:5282. doi: 10.1038/srep05282.

Abstract

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.

摘要

我们报告了瘦素启动子详细表观遗传修饰的证据以及n-3多不饱和脂肪酸(n-3 PUFAs)的作用,其与肥胖症中瘦素基因转录密切相关。在饮食诱导肥胖(DIO)小鼠的脂肪组织中,瘦素启动子处的CpG岛甲基化以及甲基-CpG结合域蛋白2(MBD2)和DNA甲基转移酶(DNMTs)的结合增加,而RNA聚合酶II减少。此外,组蛋白H3和H4发生低乙酰化,组蛋白H3的赖氨酸4(H3K4)发生低甲基化,并且在DIO小鼠的瘦素启动子处,组蛋白去乙酰化酶(HDACs)1、2和6的结合增加。这些修饰可能起到反馈作用,将瘦素浓度维持在正常范围内。n-3多不饱和脂肪酸对瘦素转录表达的调节至少部分是由表观遗传靶点介导的,如MBD2和组蛋白修饰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/801f/5381469/3724f22fe984/srep05282-f1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验