Nakamura N, Okada S
Mutat Res. 1979 Mar;60(1):83-9. doi: 10.1016/0027-5107(79)90212-4.
Synchronized mouse L5178Y cells were treated with BUdR during each one of four sequential periods of the cell cycle (M-G1, early S, middle S and late S-G2). Among the 6 markers examined, asparagine independence (Asn+), 6-thioguanine resistance (TGr) and excess thymidine resistance (TdRr) showed maximal induction of mutation rates in the early S period, methotrexate resistance (MTXr) gave maximal induction during the middle S period, and two other markers [arabinosylcytosine resistance (Ara-Cr) and ouabain resistance (Ouar)] showed little mutation induction in any period under the experimental conditions. These results suggest that (i) genes responsible for Asn+, TGr and TdRr activity may be replicated in the early S period and the gene for MTXr activity replicated in the middle S period, and (ii) the mechanisms of mutation induction for the Ouar and Ara-Cr markers may be essentially different from those for the Asn+, TGr, TdRr and MTXr markers.
同步化的小鼠L5178Y细胞在细胞周期的四个连续阶段(M-G1、早S期、中S期和晚S-G2期)的每一个阶段都用5-溴脱氧尿苷(BUdR)处理。在所检测的6个标志物中,天冬酰胺非依赖性(Asn+)、6-硫鸟嘌呤抗性(TGr)和过量胸苷抗性(TdRr)在早S期显示出最大的突变率诱导,甲氨蝶呤抗性(MTXr)在中S期诱导作用最大,另外两个标志物[阿糖胞苷抗性(Ara-Cr)和哇巴因抗性(Ouar)]在实验条件下的任何时期都显示出很少的突变诱导。这些结果表明:(i)负责Asn+、TGr和TdRr活性的基因可能在早S期复制,而负责MTXr活性的基因在中S期复制;(ii)Ouar和Ara-Cr标志物的突变诱导机制可能与Asn+、TGr、TdRr和MTXr标志物的机制本质上不同。