Oh So-Young, Park Sahng-Kyoo, Kim Jae-Woo, Ahn Yong-Ho, Park Sahng-Wook, Kim Kyung-Sup
Department of Biochemistry and Molecular Biology, Institute of Genetic Science, Yonsei University College of Medicine, 134 Shinchondong Seodaemungu, Seoul 120-752, Korea.
J Biol Chem. 2003 Aug 1;278(31):28410-7. doi: 10.1074/jbc.M300553200. Epub 2003 May 21.
Acetyl-CoA carboxylase (ACC) exists as two major isoforms originated from separate genes: ACCalpha (or ACC1) and ACCbeta (or ACC2). Previous data revealed that ACCbeta has two forms of mRNA with different 5'-untranslated regions derived by different usage of promoters, I and II, in human. In this study, we revealed that ACCbeta expression in liver is markedly stimulated by food intake at the transcriptional level. In the process of this induction in rat liver, promoter II plays the major role in regulating the expression of ACCbeta gene. The transient transfection with promoter II-luciferase reporters elucidated that the region from -93 to -38 nucleotides is important for the responsiveness to sterol regulatory element-binding protein-1 (SREBP-1), which is known to be the principle mediator for the stimulation of gene transcriptions by insulin and diet. The Sp1-binding site (-71 to -66) and neighboring two conserved SREs (-62 to -44) play a critical role in the stimulation of ACCbeta gene expression by SREBP-1. In vivo chromatin immunoprecipitation assay revealed that SREBP-1 directly bound to ACCbeta promoter II in liver, and its binding was regulated by the diet. This study provides evidence that ACCbeta expression in liver is regulated at the transcriptional level by the direct interaction of SREBP-1 with promoter II.
乙酰辅酶A羧化酶(ACC)以两种主要的同工型存在,它们起源于不同的基因:ACCα(或ACC1)和ACCβ(或ACC2)。先前的数据显示,ACCβ有两种形式的mRNA,其5'-非翻译区不同,这是由人类中启动子I和II的不同使用情况导致的。在本研究中,我们发现食物摄入在转录水平上显著刺激肝脏中ACCβ的表达。在大鼠肝脏的这种诱导过程中,启动子II在调节ACCβ基因的表达中起主要作用。用启动子II - 荧光素酶报告基因进行瞬时转染表明,从 - 93到 - 38核苷酸的区域对于对固醇调节元件结合蛋白-1(SREBP-1)的反应性很重要,已知SREBP-1是胰岛素和饮食刺激基因转录的主要介质。Sp1结合位点(-71至 - 66)和相邻的两个保守SREs(-62至 - 44)在SREBP-1刺激ACCβ基因表达中起关键作用。体内染色质免疫沉淀试验表明,SREBP-1直接与肝脏中的ACCβ启动子II结合,并且其结合受饮食调节。本研究提供了证据,表明肝脏中ACCβ的表达在转录水平上通过SREBP-1与启动子II的直接相互作用来调节。