Yahagi N, Shimano H, Hasty A H, Amemiya-Kudo M, Okazaki H, Tamura Y, Iizuka Y, Shionoiri F, Ohashi K, Osuga J, Harada K, Gotoda T, Nagai R, Ishibashi S, Yamada N
Department of Metabolic Diseases, Faculty of Medicine, University of Tokyo, Tokyo 113-8655, Japan.
J Biol Chem. 1999 Dec 10;274(50):35840-4. doi: 10.1074/jbc.274.50.35840.
Dietary polyunsaturated fatty acids (PUFA) are negative regulators of hepatic lipogenesis that exert their effects primarily at the level of transcription. Sterol regulatory element-binding proteins (SREBPs) are transcription factors responsible for the regulation of cholesterol, fatty acid, and triglyceride synthesis. In particular, SREBP-1 is known to play a crucial role in the regulation of lipogenic gene expression in the liver. To explore the possible involvement of SREBP-1 in the suppression of hepatic lipogenesis by PUFA, we challenged wild-type mice and transgenic mice overexpressing a mature form of SREBP-1 in the liver with dietary PUFA. In the liver of wild-type mice, dietary PUFA drastically decreased the mature, cleaved form of SREBP-1 protein in the nucleus, whereas the precursor, uncleaved form in the membranes was not suppressed. The decreases in mature SREBP-1 paralleled those in mRNAs for lipogenic enzymes such as fatty acid synthase and acetyl-CoA carboxylase. In the transgenic mice, dietary PUFA did not reduce the amount of transgenic SREBP-1 protein, excluding the possibility that PUFA accelerated the degradation of mature SREBP-1. The resulting sustained expression of mature SREBP-1 almost completely canceled the suppression of lipogenic gene expression by PUFA in the SREBP-1 transgenic mice. These results demonstrate that the suppressive effect of PUFA on lipogenic enzyme genes in the liver is caused by a decrease in the mature form of SREBP-1 protein, which is presumably due to the reduced cleavage of SREBP-1 precursor protein.
膳食多不饱和脂肪酸(PUFA)是肝脏脂肪生成的负调节因子,其作用主要在转录水平发挥。固醇调节元件结合蛋白(SREBP)是负责调节胆固醇、脂肪酸和甘油三酯合成的转录因子。特别是,SREBP-1在肝脏脂肪生成基因表达的调节中起着关键作用。为了探究SREBP-1是否可能参与PUFA对肝脏脂肪生成的抑制作用,我们用膳食PUFA对野生型小鼠和在肝脏中过表达成熟形式SREBP-1的转基因小鼠进行了实验。在野生型小鼠的肝脏中,膳食PUFA显著降低了细胞核中成熟的、被切割形式的SREBP-1蛋白,而膜中的前体、未切割形式并未受到抑制。成熟SREBP-1的减少与脂肪酸合成酶和乙酰辅酶A羧化酶等脂肪生成酶的mRNA减少情况平行。在转基因小鼠中,膳食PUFA并未降低转基因SREBP-1蛋白的量,排除了PUFA加速成熟SREBP-1降解的可能性。成熟SREBP-1的持续表达几乎完全消除了PUFA对SREBP-1转基因小鼠脂肪生成基因表达的抑制作用。这些结果表明,PUFA对肝脏中脂肪生成酶基因的抑制作用是由SREBP-1蛋白成熟形式的减少引起的,这可能是由于SREBP-1前体蛋白的切割减少所致。