Basson M E, Thorsness M, Rine J
Proc Natl Acad Sci U S A. 1986 Aug;83(15):5563-7. doi: 10.1073/pnas.83.15.5563.
We have isolated two genes from yeast encoding 3-hydroxy-3-methylglutaryl-coenzyme A reductase [hydroxymethylglutaryl-coenzyme A reductase (NADPH); HMG-CoA reductase; EC 1.1.1.34], the rate-limiting enzyme of sterol biosynthesis. These genes, HMG1 and HMG2, were identified by hybridization to a cDNA clone encoding hamster HMG-CoA reductase. DNA sequence analysis reveals homology between the amino acid sequence of the proteins encoded by the two yeast genes and the carboxyl-terminal half of the hamster protein. Cells containing mutant alleles of both HMG1 and HMG2 are unable to undergo spore germination and vegetative growth. However, cells containing a mutant allele of either HMG1 or HMG2 are viable but are more sensitive to compactin, a competitive inhibitor of HMG-CoA reductase, than are wild-type cells. Assays of HMG-CoA reductase activity in extracts from hmg1- and hmg2- mutants indicate that HMG1 contributes at least 83% of the activity found in wild-type cells.
我们从酵母中分离出了两个编码3-羟基-3-甲基戊二酰辅酶A还原酶[羟甲基戊二酰辅酶A还原酶(NADPH);HMG-CoA还原酶;EC 1.1.1.34]的基因,该酶是甾醇生物合成的限速酶。通过与编码仓鼠HMG-CoA还原酶的cDNA克隆杂交,鉴定出了这两个基因HMG1和HMG2。DNA序列分析揭示了这两个酵母基因编码的蛋白质的氨基酸序列与仓鼠蛋白质羧基末端一半之间的同源性。同时含有HMG1和HMG2突变等位基因的细胞无法进行孢子萌发和营养生长。然而,只含有HMG1或HMG2突变等位基因的细胞是有活力的,但比野生型细胞对HMG-CoA还原酶的竞争性抑制剂洛伐他汀更敏感。对hmg1和hmg2突变体提取物中的HMG-CoA还原酶活性进行测定表明,HMG1至少贡献了野生型细胞中发现的83%的活性。