Anderson M S, Yarger J G, Burck C L, Poulter C D
Department of Chemistry, University of Utah, Salt Lake City 84112.
J Biol Chem. 1989 Nov 15;264(32):19176-84.
Farnesyl diphosphate (FPP) synthetase is a key enzyme in isoprenoid biosynthesis which supplies C15 precursors for several classes of essential metabolites including sterols, dolichols, and ubiquinones. The structural gene for FPP synthetase was isolated on a 4.5-kilobase EcoRI genomic restriction fragment from the yeast Saccharomyces cerevisiae. The clone encodes a 40,483-dalton polypeptide of 342 amino acids with a high degree of similarity to the protein encoded by a putative rat liver clone of FPP synthetase (Clarke, C. F., Tanaka, R. D., Svenson, K., Wamsley, M., Fogelman, A. M., and Edwards, P. A. (1987) Mol. Cell Biol. 7, 3138-3146) and to an active site protein fragment from avian liver FPP synthetase (Brems, D. N., Bruenger, E., and Rilling, H. C. (1981) Biochemistry 20, 3711-3718). When cloned into the yeast shuttle vector YRp17, the 4.5-kilobase EcoRI fragment directed a 2-3-fold over-expression of FPP synthetase activity in transformed yeast cells. The levels of expression were independent of culture growth phase and orientation of the insert, indicative of a functional promoter in the clone. Disruption of the FPP synthetase gene from a diploid yeast strain, followed by dissection and analysis of tetrads, demonstrates that the gene is an essential, single copy number gene in yeast. The gene for FPP synthetase resides on chromosome XI as judged from Southern blots of separated yeast chromosomes.
法尼基二磷酸(FPP)合成酶是类异戊二烯生物合成中的关键酶,它为几类必需代谢物提供C15前体,这些代谢物包括固醇、多萜醇和泛醌。FPP合成酶的结构基因是从酿酒酵母的一个4.5千碱基的EcoRI基因组限制片段中分离出来的。该克隆编码一个由342个氨基酸组成的40483道尔顿的多肽,与推测的大鼠肝脏FPP合成酶克隆所编码的蛋白质(克拉克,C.F.,田中,R.D.,斯文森,K.,万斯利,M.,福格尔曼,A.M.,和爱德华兹,P.A.(1987年)《分子细胞生物学》7,3138 - 3146)以及禽肝脏FPP合成酶的活性位点蛋白片段(布雷姆斯,D.N.,布鲁恩格,E.,和里林,H.C.(1981年)《生物化学》20,3711 - 3718)具有高度相似性。当克隆到酵母穿梭载体YRp17中时,4.5千碱基的EcoRI片段在转化的酵母细胞中使FPP合成酶活性过表达2 - 3倍。表达水平与培养生长阶段和插入片段的方向无关,这表明克隆中有一个功能性启动子。从二倍体酵母菌株中破坏FPP合成酶基因,然后对四分体进行分离和分析,结果表明该基因在酵母中是一个必需的单拷贝基因。从分离的酵母染色体的Southern印迹判断,FPP合成酶基因位于第十一条染色体上。