Yamada Kazuya, Kawata Hiroko, Shou Zhangfei, Mizutani Tetsuya, Noguchi Tamio, Miyamoto Kaoru
Department of Biochemistry, Fukui Medical University, Japan.
J Biol Chem. 2003 Aug 15;278(33):30719-24. doi: 10.1074/jbc.M301597200. Epub 2003 Jun 7.
Transcription of the rat fatty acid synthase (FAS) gene in the rat liver can be regulated by feeding a high carbohydrate diet. A carbohydrate response element (ChoRE) located on the rat FAS gene promoter has been identified. Using multiple copies of the ChoRE as the bait in a yeast one-hybrid system, a rat liver cDNA library was screened, and the cDNA of ChoRE-binding proteins was cloned. A positive clone that encodes a basic helix-loop-helix protein, enhancer of split- and hairy-related protein-2 (SHARP-2), was obtained. Northern blot analysis revealed that the levels of SHARP-2 mRNA increase when a high carbohydrate diet is fed to normal rats or when insulin is administered to diabetic rats. In primary cultured rat hepatocytes, insulin rapidly induced an accumulation of SHARP-2 mRNA even in the absence of glucose. A time course for the increase in SHARP-2 mRNA levels indicated that it followed by those of FAS and L-type pyruvate kinase mRNAs and that the initial time course of SHARP-2 mRNA was similar to changes in the levels of glucokinase mRNA and phosphoenolpyruvate carboxykinase mRNA. Although wortmannin, LY294002, and actinomycin D blocked the increase in SHARP-2 mRNA levels by insulin, rapamycin, staurosporine, PD98059, okadaic acid, and 8-bromocyclic AMP had no effect. In addition, nuclear run-on assay revealed that transcription of the rat SHARP-2 gene was induced by insulin. Thus, we conclude that insulin induces the transcription of the rat SHARP-2 gene via a phosphoinositide 3-kinase pathway.
在大鼠肝脏中,大鼠脂肪酸合酶(FAS)基因的转录可通过给予高碳水化合物饮食来调节。已在大鼠FAS基因启动子上鉴定出一个碳水化合物反应元件(ChoRE)。利用多个ChoRE拷贝作为酵母单杂交系统中的诱饵,筛选大鼠肝脏cDNA文库,并克隆出ChoRE结合蛋白的cDNA。获得了一个编码碱性螺旋-环-螺旋蛋白、分裂和毛相关蛋白-2增强子(SHARP-2)的阳性克隆。Northern印迹分析显示,当给正常大鼠喂食高碳水化合物饮食或给糖尿病大鼠注射胰岛素时,SHARP-2 mRNA水平升高。在原代培养的大鼠肝细胞中,即使在没有葡萄糖的情况下,胰岛素也能迅速诱导SHARP-2 mRNA的积累。SHARP-2 mRNA水平升高的时间进程表明,它跟随FAS和L型丙酮酸激酶mRNA之后,且SHARP-2 mRNA的初始时间进程与葡萄糖激酶mRNA和磷酸烯醇式丙酮酸羧激酶mRNA水平的变化相似。虽然渥曼青霉素、LY294002和放线菌素D可阻断胰岛素诱导的SHARP-2 mRNA水平升高,但雷帕霉素、星形孢菌素、PD98059、冈田酸和8-溴环磷酸腺苷没有作用。此外,核转录分析显示胰岛素可诱导大鼠SHARP-2基因的转录。因此,我们得出结论,胰岛素通过磷脂酰肌醇3-激酶途径诱导大鼠SHARP-2基因的转录。