Shimano H
Department of Internal Medicine, Institute of Clinical Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8575, Japan.
Prog Lipid Res. 2001 Nov;40(6):439-52. doi: 10.1016/s0163-7827(01)00010-8.
Roles of sterol regulatory element-binding proteins (SREBPs) have been established as lipid synthetic transcription factors especially for cholesterol and fatty acid synthesis. SREBPs have unique characteristics. Firstly, they are membrane-bound proteins and the N-terminal active portions enter nucleus to activate their target genes after proteolytic cleavage, which requires sterol-sensing molecule, SREBP-activating protein (SCAP) and is crucial for sterol-regulation. Secondly, they bind and activate sterol-regulatory (SREs) containing promoters as well as some E-boxes, which makes SREBPs eligible to regulate a wide range of lipid genes. Finally, three isoforms, SREBP-1a-1c, and have different roles in lipid synthesis. In vivo studies using transgenic and knockout mice suggest that SREBP-1 seems to be involved in energy metabolism including fatty acid and glucose/insulin metabolism, whereas SREBP-2 is specific to cholesterol synthesis. Future studies will be focused on understanding molecular mechanisms sensing cellular sterol and energy states where SREBPs are deeply involved.
固醇调节元件结合蛋白(SREBPs)的作用已被确认为脂质合成转录因子,特别是在胆固醇和脂肪酸合成方面。SREBPs具有独特的特性。首先,它们是膜结合蛋白,其N端活性部分在蛋白水解切割后进入细胞核以激活其靶基因,这需要固醇感应分子、SREBP激活蛋白(SCAP),并且对固醇调节至关重要。其次,它们结合并激活含有启动子以及一些E盒的固醇调节元件(SREs),这使得SREBPs有资格调节广泛的脂质基因。最后,三种异构体SREBP-1a - 1c在脂质合成中具有不同的作用。使用转基因和基因敲除小鼠的体内研究表明,SREBP-1似乎参与能量代谢,包括脂肪酸和葡萄糖/胰岛素代谢,而SREBP-2则特异性参与胆固醇合成。未来的研究将集中于理解SREBPs深度参与的感知细胞固醇和能量状态的分子机制。