Franks D J, Whitfield J F, Durkin J P
J Cell Biochem. 1987 Feb;33(2):87-94. doi: 10.1002/jcb.240330203.
Rat kidney (NRK) cells infected with a temperature-sensitive mutant of the Kirsten sarcoma virus were arrested in the G0/G1 phase of their cell cycle by incubation in serum-deficient medium at a p21-inactivating temperature of 41 degrees C. These quiescent ts K-NRK cells were then stimulated to transit G1 and initiate DNA replication by lowering the temperature to 36 degrees C, which rapidly reactivated p21. Reactivating the viral Ki-RAS protein by temperature shift led to an increase in adenylate cyclase activity in early G1 phase. The Ki-RAS protein increased the sensitivity of adenylate cyclase to guanyl nucleotides by a mechanism that seemed to involve inactivation of the enzyme's inhibitory G1 regulatory protein.
感染了柯斯顿肉瘤病毒温度敏感突变体的大鼠肾(NRK)细胞,通过在无血清培养基中于41摄氏度(p21失活温度)孵育,被阻滞在细胞周期的G0/G1期。然后,通过将温度降至36摄氏度(该温度能迅速重新激活p21),刺激这些静止的ts K-NRK细胞进入G1期并启动DNA复制。通过温度转换重新激活病毒Ki-RAS蛋白会导致G1早期腺苷酸环化酶活性增加。Ki-RAS蛋白通过一种似乎涉及使该酶的抑制性G1调节蛋白失活的机制,增加了腺苷酸环化酶对鸟苷核苷酸的敏感性。