Chu E H, McLaren J D, Li I C, Lamb B
Biochem Genet. 1984 Aug;22(7-8):701-15. doi: 10.1007/BF00485854.
Following chemical mutagenesis and multiple-step indirect selection, four clones of Chinese hamster V79 cells were isolated which exhibited auxotrophy for thymidine, deoxycytidine, or deoxyuridine but not for cytidine or uridine. All were resistant to uridine, 3-deazauridine, 5-fluorouridine, thymidine, and cytosine arabinoside at concentrations that were toxic to wild-type V79 cells. The cytidine 5'-triphosphate (CTP) and deoxycytidine 5'-triphosphate (dCTP) pools in the mutants were expanded, but the uridine 5'-triphosphate (UTP) pool either decreased or remained unchanged relative to the wild-type level. Furthermore, since the parental cells appear to be deficient in dCMP deaminase activity and CTP (or one of its metabolites) has been shown to inhibit uridine 5'-diphosphate (UDP) reduction, an elevated CTP level should lead to the observed thymidine auxotrophy. It also explains the joint resistance of mutant clones to thymidine and cytosine arabinoside. The change in the ratio of intracellular dCTP to thymidine 5'-triphosphate (dTTP) may be responsible for the elevation in the rates of spontaneous mutations in these mutants.
经过化学诱变和多步间接筛选,分离出了四个中国仓鼠V79细胞克隆,它们对胸苷、脱氧胞苷或脱氧尿苷表现出营养缺陷型,但对胞苷或尿苷无此现象。所有克隆对尿苷、3-脱氮尿苷、5-氟尿苷、胸苷和阿糖胞苷均具有抗性,而这些物质在野生型V79细胞中会产生毒性。与野生型水平相比,突变体中的胞苷5'-三磷酸(CTP)和脱氧胞苷5'-三磷酸(dCTP)池有所扩大,但尿苷5'-三磷酸(UTP)池要么减少,要么保持不变。此外,由于亲代细胞似乎缺乏dCMP脱氨酶活性,且CTP(或其一种代谢物)已被证明可抑制尿苷5'-二磷酸(UDP)还原,因此CTP水平升高应会导致观察到的胸苷营养缺陷型。这也解释了突变克隆对胸苷和阿糖胞苷的联合抗性。细胞内dCTP与胸苷5'-三磷酸(dTTP)比例的变化可能是这些突变体自发突变率升高的原因。