Wawra E, Wintersberger E
Mol Cell Biol. 1983 Mar;3(3):297-304. doi: 10.1128/mcb.3.3.297-304.1983.
Cell-free DNA synthesis was performed in a lysed cell system from mouse cell cultures. The in vitro reaction was totally inhibited by N-ethylmaleimide but unaffected by hydroxyurea or fluorodeoxyuridine when these compounds were added to the incubation mixture. However, in a preparation obtained from cells which had been blocked by hydroxyurea before lysis, the rate of DNA synthesis was markedly reduced. This effect could not have been caused by the depletion of the precursor pools as all necessary triphosphates were added to the in vitro incubation mixture. Analysis by alkaline density gradients showed that the ligation of primary synthesis products is retarded in hydroxyurea-pretreated lysed cells and that small fragments accumulate. These results suggest that hydroxyurea interferes with the processing of early replication products, preventing the formation of longer intermediates. Its mechanism is either independent from the well-known inhibition of ribonucleoside diphosphate reductase or it may be the result of an as-yet-unknown function of this enzyme in a later step of replication. This observation could help to explain why cells appear to be blocked by hydroxyurea in the early part of the S phase (rather than at the G1/S border proper) and also why DNA repair synthesis is relatively insensitive to the drug.
无细胞DNA合成在来自小鼠细胞培养物的裂解细胞系统中进行。当将这些化合物添加到孵育混合物中时,体外反应完全被N-乙基马来酰亚胺抑制,但不受羟基脲或氟脱氧尿苷的影响。然而,在从裂解前已被羟基脲阻断的细胞中获得的制剂中,DNA合成速率明显降低。这种效应不可能是由于前体池的耗尽引起的,因为所有必需的三磷酸都添加到了体外孵育混合物中。通过碱性密度梯度分析表明,在羟基脲预处理的裂解细胞中,初级合成产物的连接受到阻碍,并且小片段积累。这些结果表明,羟基脲干扰早期复制产物的加工,阻止形成更长的中间体。其机制要么独立于众所周知的核糖核苷二磷酸还原酶的抑制作用,要么可能是该酶在复制后期的一个尚未知晓的功能的结果。这一观察结果有助于解释为什么细胞似乎在S期早期被羟基脲阻断(而不是在G1/S边界本身),以及为什么DNA修复合成对该药物相对不敏感。