Nicander B, Reichard P
Proc Natl Acad Sci U S A. 1983 Mar;80(5):1347-51. doi: 10.1073/pnas.80.5.1347.
The 3H-labeled nucleosides cytidine, deoxycytidine, and thymidine are rapidly incorporated into DNA via dCTP or dTTP pools. Between 30 and 60 min after addition of tracer amounts of a labeled nucleoside to the medium of rapidly growing 3T6 cells, dNTP pools attained a constant specific activity resulting from a steady-state equilibrium between incorporation of nucleoside, de novo synthesis, and linear incorporation of isotope into DNA. Removal of labeled deoxycytidine or thymidine depleted the dNTP pools of isotope within a few minutes and incorporation into DNA stopped. When de novo synthesis of dTTP was blocked with amethopterin, the intracellular dTTP pool rapidly reached the specific activity of thymidine of the medium and isotope incorporation into DNA then measured absolute rates of DNA synthesis. In experiments with and without amethopterin, we found no kinetic evidence for the existence of more than one dTTP pool and the decay of the pool suggested that all dTTP served as precursor of DNA. In contrast, experiments with deoxycytidine and cytidine suggested the presence of separate dCTP pools with preferential DNA synthesis from the pool labeled from cytidine.
3H标记的核苷胞苷、脱氧胞苷和胸苷通过dCTP或dTTP库迅速掺入DNA。在向快速生长的3T6细胞培养基中加入示踪量的标记核苷后30至60分钟内,dNTP库达到恒定的比活性,这是由于核苷掺入、从头合成以及同位素线性掺入DNA之间的稳态平衡所致。去除标记的脱氧胞苷或胸苷会在几分钟内耗尽dNTP库中的同位素,并且DNA掺入停止。当用氨甲蝶呤阻断dTTP的从头合成时,细胞内dTTP库迅速达到培养基中胸苷的比活性,然后将同位素掺入DNA中以测量DNA合成的绝对速率。在有和没有氨甲蝶呤的实验中,我们没有发现动力学证据表明存在不止一个dTTP库,并且该库的衰减表明所有dTTP都作为DNA的前体。相比之下,用脱氧胞苷和胞苷进行的实验表明存在单独的dCTP库,且优先从胞苷标记的库中进行DNA合成。