Kern L, de Montigny J, Jund R, Lacroute F
Laboratoire de Génétique Physiologique, Institut de Biologie Moléculaire et Cellulaire du C.N.R.S., Strasbourg, France.
Gene. 1990 Apr 16;88(2):149-57. doi: 10.1016/0378-1119(90)90026-n.
The FUR1 gene of Saccharomyces cerevisiae encodes uracil phosphoribosyltransferase (UPRTase) which catalyses the conversion of uracil into uridine 5'-monophosphate (UMP) in the pyrimidine salvage pathway. The FUR1 gene is included in a 2.1 kb genomic segment of DNA and is transcribed into a 1 kb poly(A)+mRNA. Sequencing has determined a 753 bp open reading frame capable of encoding a protein of 251 amino acids. The FUR1 genes for three recessive fur1 alleles, having different sensibilities to 5-fluorouridine (5-FUR) but identical levels of resistance to 5-fluorouracil (5-FU), were cloned and sequenced. Single bp changes located in different regions of the gene were found in each mutant. Two in vitro-constructed deletions of the FUR1 gene have been integrated at the chromosomal locus, giving strains with 5-FURR and 5-FURR mutant phenotype. Assays of UPRTase, uridine kinase, uridine ribohydrolase and uridine 5'-monophosphate nucleotidase enzymatic activities, in extracts of strains where the FUR1 gene is overexpressed or deleted, indicate that the FUR1 encoded protein possesses only UPRTase activity.
酿酒酵母的FUR1基因编码尿嘧啶磷酸核糖转移酶(UPRTase),该酶在嘧啶补救途径中催化尿嘧啶转化为尿苷5'-单磷酸(UMP)。FUR1基因包含在一个2.1 kb的基因组DNA片段中,并转录成一个1 kb的聚腺苷酸加尾mRNA。测序确定了一个753 bp的开放阅读框,能够编码一个由251个氨基酸组成的蛋白质。对三个隐性fur1等位基因的FUR1基因进行了克隆和测序,这些等位基因对5-氟尿苷(5-FUR)具有不同的敏感性,但对5-氟尿嘧啶(5-FU)的抗性水平相同。在每个突变体中都发现了位于基因不同区域的单碱基变化。两个体外构建的FUR1基因缺失已整合到染色体位点,产生具有5-FURR和5-FURR突变表型的菌株。在FUR1基因过表达或缺失的菌株提取物中,对UPRTase、尿苷激酶、尿苷核糖水解酶和尿苷5'-单磷酸核苷酸酶的酶活性进行测定,结果表明FUR1编码的蛋白质仅具有UPRTase活性。