Grummt F
Proc Natl Acad Sci U S A. 1978 Jan;75(1):371-5. doi: 10.1073/pnas.75.1.371.
Addition of diadenosine 5',5'''-P1,P4-tetraphosphate (Ap4A) to permeabilized G1-arrested baby hamster kidney cells resulted in the stimulation of DNA synthesis. No stimulation was observed in cells from exponentially growing cultures. The Ap4A-stimulated [3H]dTTP incorporation was inhibited by nalidixic acid, daunomycin, chloroquine diphosphate, EDTA, and N-ethylmaleimide. It was dose-dependent in regard to the amount of permeabilized cells and of Ap4A. Numerous replication eyes were formed in the DNA molecules of stimulated cells. Pulse-chase experiments showed that the synthesis of DNA was discontinuous, resulting in the appearance of approximately 4S Okazaki fragments and their ligation to high molecular weight DNA. These results strongly suggest that Ap4A stimulated the initiation of DNA synthesis in baby hamster kidney cells that had been arrested in G1 by serum deprival.
向经通透处理并停滞于G1期的幼仓鼠肾细胞中添加5',5'''-P1,P4-四磷酸二腺苷(Ap4A)可刺激DNA合成。在指数生长期培养的细胞中未观察到刺激作用。Ap4A刺激的[3H]dTTP掺入受到萘啶酸、柔红霉素、二磷酸氯喹、乙二胺四乙酸(EDTA)和N-乙基马来酰亚胺的抑制。其在通透细胞和Ap4A的量方面呈剂量依赖性。在受刺激细胞的DNA分子中形成了许多复制眼。脉冲追踪实验表明,DNA合成是不连续的,导致出现约4S的冈崎片段并将其连接成高分子量DNA。这些结果有力地表明,Ap4A刺激了因血清剥夺而停滞于G1期的幼仓鼠肾细胞中DNA合成的起始。