Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Prog Lipid Res. 2011 Oct;50(4):403-10. doi: 10.1016/j.plipres.2011.07.002. Epub 2011 Jul 23.
HMG-CoA reductase (HMGR), a highly conserved, membrane-bound enzyme, catalyzes a rate-limiting step in sterol and isoprenoid biosynthesis and is the primary target of hypocholesterolemic drug therapy. HMGR activity is tightly regulated to ensure maintenance of lipid homeostasis, disruption of which is a major cause of human morbidity and mortality. HMGR regulation takes place at the levels of transcription, translation, post-translational modification and degradation. In this review, we discuss regulation of mammalian, Saccharomyces cerevisiae and Schizosaccharomyces pombe HMGR and highlight recent advances in the field. We find that the general features of HMGR regulation, including a requirement for the HMGR-binding protein Insig, are remarkably conserved between mammals and ascomycetous fungi, including S. cerevisiae and S. pombe. However the specific details by which this regulation occurs differ in surprising ways, revealing the broad evolutionary themes underlying both HMGR regulation and Insig function.
羟甲基戊二酰辅酶 A 还原酶(HMGR)是一种高度保守的膜结合酶,催化甾醇和异戊烯焦磷酸生物合成的限速步骤,是降胆固醇药物治疗的主要靶点。HMGR 活性受到严格调控,以确保脂质稳态的维持,其破坏是人类发病率和死亡率的主要原因。HMGR 的调控发生在转录、翻译、翻译后修饰和降解等水平。在这篇综述中,我们讨论了哺乳动物、酿酒酵母和裂殖酵母 HMGR 的调控,并强调了该领域的最新进展。我们发现,HMGR 调控的一般特征,包括 HMGR 结合蛋白 Insig 的需求,在哺乳动物和子囊菌(包括酿酒酵母和裂殖酵母)之间是非常保守的。然而,这种调控发生的具体细节却以惊人的方式有所不同,揭示了 HMGR 调控和 Insig 功能的广泛进化主题。