Wojcik B E, Dermody J J, Ozer H L, Mun B, Mathews C K
Department of Biological Science, Hunter College, City University of New York, New York 10021.
Mol Cell Biol. 1990 Nov;10(11):5688-99. doi: 10.1128/mcb.10.11.5688-5699.1990.
JB3-B is a Chinese hamster ovary cell mutant previously shown to be temperature sensitive for DNA replication (J. J. Dermody, B. E. Wojcik, H. Du, and H. L. Ozer, Mol. Cell. Biol. 6:4594-4601, 1986). It was chosen for detailed study because of its novel property of inhibiting both polyomavirus and adenovirus DNA synthesis in a temperature-dependent manner. Pulse-labeling studies demonstrated a defect in the rate of adenovirus DNA synthesis. Measurement of deoxyribonucleoside triphosphate (dNTP) pools as a function of time after shift of uninfected cultures from 33 to 39 degrees C revealed that all four dNTP pools declined at similar rates in extracts prepared either from whole cells or from rapidly isolated nuclei. Ribonucleoside triphosphate pools were unaffected by a temperature shift, ruling out the possibility that the mutation affects nucleoside diphosphokinase. However, ribonucleotide reductase activity, as measured in extracts, declined after cell cultures underwent a temperature shift, in parallel with the decline in dNTP pool sizes. Moreover, the activity of cell extracts was thermolabile in vitro, consistent with the model that the JB3-B mutation affects the structural gene for one of the ribonucleotide reductase subunits. The kinetics of dNTP pool size changes after temperature shift are quite distinct from those reported after inhibition of ribonucleotide reductase with hydroxyurea. An indirect effect on ribonucleotide reductase activity in JB3-B has not been excluded since human sequences other than those encoding the enzyme subunits can correct the temperature-sensitive growth defect in the mutant.
JB3 - B是一种中国仓鼠卵巢细胞突变体,先前已证明其对DNA复制具有温度敏感性(J. J. 德莫迪、B. E. 沃伊西克、H. 杜和H. L. 奥泽,《分子细胞生物学》6:4594 - 4601,1986年)。由于其具有以温度依赖方式抑制多瘤病毒和腺病毒DNA合成的新特性,所以被选作详细研究对象。脉冲标记研究表明腺病毒DNA合成速率存在缺陷。对未感染培养物从33℃转移至39℃后不同时间的脱氧核糖核苷三磷酸(dNTP)池进行测量发现,无论是从全细胞还是从快速分离的细胞核制备的提取物中,所有四种dNTP池均以相似速率下降。核糖核苷三磷酸池不受温度变化影响,排除了该突变影响核苷二磷酸激酶的可能性。然而,在细胞培养物经历温度变化后,提取物中测得的核糖核苷酸还原酶活性下降,与dNTP池大小的下降平行。此外,细胞提取物的活性在体外具有热不稳定性,这与JB3 - B突变影响核糖核苷酸还原酶亚基之一的结构基因的模型一致。温度变化后dNTP池大小变化的动力学与用羟基脲抑制核糖核苷酸还原酶后报道的动力学有很大不同。由于除了编码酶亚基的序列外,人类其他序列可以纠正该突变体的温度敏感生长缺陷,所以尚未排除对JB3 - B中核糖核苷酸还原酶活性的间接影响。