Nishida Y, Yasuda S, Sekiguchi M
Biochim Biophys Acta. 1976 Aug 18;442(2):208-15. doi: 10.1016/0005-2787(76)90491-3.
A highly purified preparation of T4 endonuclease V does not degrade DNA alkylated with methyl methanesulfonate, and the methyl methanesulfonate sensitivity of T4 wild type and x mutant is not affected by the v mutation. Thus, T4 endonuclease V, the v gene product, does not seem to be involved in a repair or an abortive repair of methyl methanesulfonate-damaged T4 DNA. The x and y genes of T4 and the polA and the uvrD genes of Escherichia coli are concerned with the repair of methyl methanesulfonate-induced damages in T4 DNA. Since effects of the polA and the x or y mutations are additive, it is supposed that there are at least two pathways for the repair of methyl meth-anesulfonate-damaged T4 DNA, one controlled by the x and the y genes and the other in which E. coli DNA olymerase I is involved. The partial suppression of the x gene mutation at high temerature was also demonstrated.
高度纯化的T4内切核酸酶V制剂不会降解被甲磺酸甲酯烷基化的DNA,并且T4野生型和x突变体对甲磺酸甲酯的敏感性不受v突变的影响。因此,T4内切核酸酶V(v基因产物)似乎不参与甲磺酸甲酯损伤的T4 DNA的修复或流产修复。T4的x和y基因以及大肠杆菌的polA和uvrD基因与甲磺酸甲酯诱导的T4 DNA损伤的修复有关。由于polA与x或y突变的效应是累加的,因此推测甲磺酸甲酯损伤的T4 DNA的修复至少有两条途径,一条由x和y基因控制,另一条涉及大肠杆菌DNA聚合酶I。还证明了在高温下x基因突变的部分抑制。