Snow E T, Foote R S, Mitra S
Biochemistry. 1984 Sep 11;23(19):4289-94. doi: 10.1021/bi00314a006.
O6-Methyldeoxyguanosine triphosphate (m6dGTP), known to be produced in vivo by methylation of deoxyguanosine triphosphate with simple methylating mutagens, is utilized by prokaryotic DNA polymerases during in vitro replication of synthetic and natural DNA template-primers. A study of the kinetic behavior of m6dGTP during DNA replication in vitro and of its effect on DNA replication indicates that m6dGTP acts as an analogue of dATP with Kappm of about 6 microM for Escherichia coli DNA polymerase I (Klenow fragment) compared to the Kappm of about 0.8 microM for dATP. m6dGTP is not incorporated in the complete absence of dATP (a competitive inhibitor). m6dGTP also inhibits in vitro DNA synthesis. Different DNA polymerases behave differently in utilization and turnover of m6dGTP. T4 DNA polymerase shows stronger discrimination against m6dGMP incorporation than either T5 DNA polymerase or E. coli DNA polymerase I. The possibility that m6dGTP is unlikely to contribute significantly to in vivo mutation is discussed.
O6-甲基脱氧鸟苷三磷酸(m6dGTP)已知在体内由脱氧鸟苷三磷酸与简单甲基化诱变剂甲基化产生,在合成和天然DNA模板引物的体外复制过程中被原核DNA聚合酶利用。一项关于m6dGTP在体外DNA复制过程中的动力学行为及其对DNA复制影响的研究表明,m6dGTP作为dATP的类似物,与dATP约0.8 microM的表观解离常数(Kappm)相比,大肠杆菌DNA聚合酶I(Klenow片段)对其的表观解离常数约为6 microM。在完全没有dATP(一种竞争性抑制剂)的情况下,m6dGTP不会被掺入。m6dGTP也抑制体外DNA合成。不同的DNA聚合酶在m6dGTP的利用和周转方面表现不同。T4 DNA聚合酶对m6dGMP掺入的识别能力比T5 DNA聚合酶或大肠杆菌DNA聚合酶I更强。文中讨论了m6dGTP不太可能对体内突变有显著贡献的可能性。