School of Biotechnology and Biomolecular Sciences, The University of New South Wales, Sydney, NSW, Australia.
National Center for Protein Sciences, State Key Laboratory of Molecular Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Prog Lipid Res. 2016 Oct;64:138-151. doi: 10.1016/j.plipres.2016.09.003. Epub 2016 Sep 30.
The conversion of 7-dehydrocholesterol to cholesterol, the final step of cholesterol synthesis in the Kandutsch-Russell pathway, is catalyzed by the enzyme 7-dehydrocholesterol reductase (DHCR7). Homozygous or compound heterozygous mutations in DHCR7 lead to the developmental disease Smith-Lemli-Opitz syndrome, which can also result in fetal mortality, highlighting the importance of this enzyme in human development and survival. Besides serving as a substrate for DHCR7, 7-dehydrocholesterol is also a precursor of vitamin D via the action of ultraviolet light on the skin. Thus, DHCR7 exerts complex biological effects, involved in both cholesterol and vitamin D production. Indeed, we argue that DHCR7 can act as a switch between cholesterol and vitamin D synthesis. This review summarizes current knowledge about the critical enzyme DHCR7, highlighting recent findings regarding its structure, transcriptional and post-transcriptional regulation, and its links to vitamin D synthesis. Greater understanding about DHCR7 function, regulation and its place within cellular metabolism will provide important insights into its biological roles.
7-脱氢胆固醇向胆固醇的转化是坎德彻-拉塞尔途径中胆固醇合成的最后一步,该反应由 7-脱氢胆固醇还原酶(DHCR7)催化。DHCR7 的纯合或复合杂合突变会导致发育性疾病史密斯-林利-欧皮茨综合征,也可能导致胎儿死亡,这凸显了该酶在人类发育和生存中的重要性。除了作为 DHCR7 的底物外,7-脱氢胆固醇也是通过皮肤暴露于紫外线而产生维生素 D 的前体。因此,DHCR7 发挥着复杂的生物学效应,既参与胆固醇的产生,也参与维生素 D 的产生。事实上,我们认为 DHCR7 可以作为胆固醇和维生素 D 合成之间的转换开关。本综述总结了关于关键酶 DHCR7 的现有知识,重点介绍了其结构、转录和转录后调控以及与维生素 D 合成相关的最新发现。对 DHCR7 功能、调控及其在细胞代谢中的位置的进一步了解,将为深入了解其生物学作用提供重要线索。