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脂肪细胞决定和分化依赖因子1/固醇调节元件结合蛋白1c调节小鼠脂联素表达。

Adipocyte determination- and differentiation-dependent factor 1/sterol regulatory element-binding protein 1c regulates mouse adiponectin expression.

作者信息

Seo Jong Bae, Moon Hyang Mi, Noh Mun Ju, Lee Yun Sok, Jeong Hyun Woo, Yoo Eung Jae, Kim Woo Sik, Park Jiyoung, Youn Byung-S, Kim Jae Woo, Park Sang Dai, Kim Jae Bum

机构信息

School of Biological Sciences, Seoul National University, Seoul, Korea 151-742.

出版信息

J Biol Chem. 2004 May 21;279(21):22108-17. doi: 10.1074/jbc.M400238200. Epub 2004 Mar 22.

Abstract

Adiponectin is exclusively expressed in differentiated adipocytes and plays an important role in regulating energy homeostasis, including the glucose and lipid metabolism associated with increased insulin sensitivity. However, the control of adiponectin gene expression in adipocytes is poorly understood. We show here that levels of adiponectin mRNA and protein are reduced in the white adipose tissue of ob/ob and db/db mice and that there is a concomitant reduction of the adipocyte determination- and differentiation-dependent factor 1 (ADD1)/sterol regulatory element-binding protein 1c (SREBP1c) transcription factor. To determine whether ADD1/SREBP1c regulates adiponectin gene expression, we isolated and characterized the mouse adiponectin promoter. Analysis of the adiponectin promoter revealed putative binding sites for the adipogenic transcription factors ADD1/SREBP1c, peroxisomal proliferator-activated receptor gamma and CCAAT enhancer-binding proteins. DNase I footprinting and chromatin immunoprecipitation analyses revealed that ADD1/SREBP1c binds in vitro and in vivo to the proximal promoter containing sterol regulatory element (SRE) motifs. A luciferase reporter containing the promoter was transactivated by ADD1/SREBP1c, and introduction of SRE mutations into the construct abolished transactivation. Adenoviral overexpression of ADD1/SREBP1c also elevated adiponectin mRNA and protein levels in 3T3-L1 adipocytes. Furthermore, insulin stimulated adiponectin mRNA expression in adipocytes and augmented transactivation of the adiponectin promoter by ADD1/SREBP1c. Taken together, these data indicate that ADD1/SREBP1c controls adiponectin gene expression in differentiated adipocytes.

摘要

脂联素仅在分化的脂肪细胞中表达,在调节能量平衡中发挥重要作用,包括与胰岛素敏感性增加相关的葡萄糖和脂质代谢。然而,脂肪细胞中脂联素基因表达的调控机制尚不清楚。我们在此表明,ob/ob和db/db小鼠白色脂肪组织中脂联素mRNA和蛋白质水平降低,同时脂肪细胞决定和分化依赖性因子1(ADD1)/固醇调节元件结合蛋白1c(SREBP1c)转录因子也相应减少。为了确定ADD1/SREBP1c是否调节脂联素基因表达,我们分离并鉴定了小鼠脂联素启动子。对脂联素启动子的分析揭示了成脂转录因子ADD1/SREBP1c、过氧化物酶体增殖物激活受体γ和CCAAT增强子结合蛋白的假定结合位点。DNase I足迹分析和染色质免疫沉淀分析表明,ADD1/SREBP1c在体外和体内均与含有固醇调节元件(SRE)基序的近端启动子结合。含有该启动子的荧光素酶报告基因被ADD1/SREBP1c反式激活,并且将SRE突变引入构建体中可消除反式激活。ADD1/SREBP1c的腺病毒过表达也提高了3T3-L1脂肪细胞中脂联素mRNA和蛋白质水平。此外,胰岛素刺激脂肪细胞中脂联素mRNA表达,并增强ADD1/SREBP1c对脂联素启动子的反式激活。综上所述,这些数据表明ADD1/SREBP1c控制分化脂肪细胞中脂联素基因的表达。

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