Deng Xiong, Cagen Lauren M, Wilcox Henry G, Park Edwards A, Raghow Rajendra, Elam Marshall B
Department of Veterans Affairs Medical Center, Memphis, Tennessee, USA.
Biochem Biophys Res Commun. 2002 Jan 11;290(1):256-62. doi: 10.1006/bbrc.2001.6148.
We have cloned 5 kb of genomic DNA encompassing 1.72 kb of 5'-regulatory sequence and exons 1-c and 2 of the rat SREBP-1c gene. A 1.5-kb segment upstream from the transcription start site was ligated ahead of the luciferase reporter gene and tested for promoter activity by transient transfection assays in primary rat hepatocytes. We discovered that insulin strongly activated the full-length promoter, regardless of whether 5 or 20 mM glucose was in the culture medium during treatment. Stimulation by insulin was blocked by dibutyryl-cAMP and by polyunsaturated fatty acids, such as alpha-linolenic acid, gamma-linolenic acid, or eicosapentaenoic acid; palmitic or oleic acids, however, had no inhibitory effect. A truncated promoter containing 149 bp of 5' flanking DNA, including proximal NF-Y, E-box, SRE, and Sp1 sites, retained most of the response. This is the first report that insulin, cAMP, and polyunsaturated fatty acids modulate the proximal SREBP-1c promoter in rat hepatocytes mirroring physiological regulation of SREBP-1c in vivo.
我们克隆了5kb的基因组DNA,其中包含1.72kb的5'-调控序列以及大鼠SREBP-1c基因的外显子1-c和2。在荧光素酶报告基因之前连接转录起始位点上游1.5kb的片段,并通过原代大鼠肝细胞中的瞬时转染试验检测其启动子活性。我们发现,无论在处理过程中培养基中的葡萄糖浓度是5mM还是20mM,胰岛素都能强烈激活全长启动子。胰岛素的刺激作用被二丁酰-cAMP和多不饱和脂肪酸(如α-亚麻酸、γ-亚麻酸或二十碳五烯酸)阻断;然而,棕榈酸或油酸没有抑制作用。一个包含149bp 5'侧翼DNA的截短启动子,包括近端NF-Y、E-box、SRE和Sp1位点,保留了大部分反应。这是首次报道胰岛素、cAMP和多不饱和脂肪酸在大鼠肝细胞中调节近端SREBP-1c启动子,反映了体内SREBP-1c的生理调节。