Ozier-Kalogeropoulos O, Fasiolo F, Adeline M T, Collin J, Lacroute F
Centre de Génétique Moléculaire du C.N.R.S. Université Pierre et Marie Curie, Gif-sur-Yvette, France.
Mol Gen Genet. 1991 Dec;231(1):7-16. doi: 10.1007/BF00293815.
The URA7 gene of Saccharomyces cerevisiae encodes CTP synthetase (EC 6.3.4.2) which catalyses the conversion of uridine 5'-triphosphate to cytidine 5'-triphosphate, the last step of the pyrimidine biosynthetic pathway. We have cloned and sequenced the URA7 gene. The coding region is 1710 bp long and the deduced protein sequence shows a strong degree of homology with bacterial and human CTP synthetases. Gene disruption shows that URA7 is not an essential gene: the level of the intracellular CTP pool is roughly the same in the deleted and the wild-type strains, suggesting that an alternative pathway for CTP synthesis exists in yeast. This could involve either a divergent duplicated gene or a different route beginning with the amination of uridine mono- or diphosphate.
酿酒酵母的URA7基因编码CTP合成酶(EC 6.3.4.2),该酶催化尿苷5'-三磷酸转化为胞苷5'-三磷酸,这是嘧啶生物合成途径的最后一步。我们已经克隆并测序了URA7基因。编码区长度为1710 bp,推导的蛋白质序列与细菌和人类的CTP合成酶具有高度同源性。基因破坏表明URA7不是必需基因:缺失菌株和野生型菌株中细胞内CTP池的水平大致相同,这表明酵母中存在CTP合成的替代途径。这可能涉及一个不同的重复基因或一条从尿苷单磷酸或二磷酸胺化开始的不同途径。