Collins A, Oates D J
Department of Zoology, University of Cambridge.
Eur J Biochem. 1987 Dec 1;169(2):299-305. doi: 10.1111/j.1432-1033.1987.tb13612.x.
We have measured deoxyribonucleotide pool sizes in different cell types: normal human, transformed human (HeLa), and the permanent hamster line CHO-K1. The range of sizes of the four DNA precursor pools in CHO cells is far greater than in human cells. It is a general rule that hydroxyurea causes rapid depletion of pools (except for dTTP) until the pool present in smallest amount is exhausted; this suggests a tight coupling of the pools to DNA replication (the presumed main cause of the depletion). The effect of hydroxyurea on DNA repair after ultraviolet irradiation (namely, a relatively small accumulation of incomplete repair sites blocked at the resynthesis stage) is probably accounted for by the reduced availability of DNA precursors. However, depletion of the dCTP pool is not an adequate explanation for the observed enhancement by hydroxyurea of the inhibitory effect of cytosine arabinoside; we suggest other possible modes of action. Ultraviolet irradiation has only small effects on the levels of deoxyribonucleotides.
正常人细胞、转化的人细胞(HeLa)以及仓鼠永久性细胞系CHO-K1。CHO细胞中四种DNA前体库的大小范围远大于人细胞。一般规律是,羟基脲会导致库(dTTP除外)迅速耗尽,直到含量最少的库被耗尽;这表明库与DNA复制紧密相关(推测是耗尽的主要原因)。羟基脲对紫外线照射后DNA修复的影响(即在再合成阶段受阻的不完全修复位点相对少量积累)可能是由于DNA前体可用性降低所致。然而,dCTP库的耗尽并不能充分解释观察到的羟基脲增强阿糖胞苷抑制作用的现象;我们提出了其他可能的作用模式。紫外线照射对脱氧核苷酸水平的影响很小。