Deoxyribenucleoside triphosphate (dNTP) pools were measured in normal BALB/c3T3 cells, transformation-treated cells and transformed cells with reverse-phase HPLC. The fluctuation of dNTP pools was similar after transf...Deoxyribenucleoside triphosphate (dNTP) pools were measured in normal BALB/c3T3 cells, transformation-treated cells and transformed cells with reverse-phase HPLC. The fluctuation of dNTP pools was similar after transformation treatment with alkylating mutagen glycidyl methacrylate(GMA) or Nmethyl- N'- nitro N- nitrosoguanidine (MNNG ). However,the gap between deoxyguanosine triphosphate + deoxyadenosine triphosphate (dGTP + dATP) pools and deoxythymidine triphosphate + deoxycytidine triphosphate (dTTP + dCTP) pools was greatly intensified. The measurements also indicated that the dNTP pools in transformed cells were quite different from those in normal cells. The results suggested that dNTP pools may play an important role in cell transformation展开更多
The induced mutation frequency by alkylating mutagen glycldyl methacrylate (GMA) and N-methyl-N'- nitro- N-nitrosoguanidine (MNNG) was investigated with or without perturbation of deoxyribenucleoside triphosphate ...The induced mutation frequency by alkylating mutagen glycldyl methacrylate (GMA) and N-methyl-N'- nitro- N-nitrosoguanidine (MNNG) was investigated with or without perturbation of deoxyribenucleoside triphosphate (dNTP)pools; the influence of short treatment at different concentrations of GMA or MNNG on dNTP pools was also explored. The results indicated that the induced mutation frequency increased greatly at high dosages of mutagen (GMA~ 64 μg/ml, MNNG~ 8 μg/ml) and the perturbation on dNTP pools was carried out before the treatment of mutagen; the short treatment with mutagen could induce distinct fluctuations of dNTP pools, but different mutagen might have different effects on dNTP pools.According to the results of the present study and other reports in literature, we conclude that dNTP pools may be the targets of alkylating mutagens and the fluctuations of dNTP pools are closely associated with mutagenesis展开更多
Effects of Mg^2＋, NTPs and Taq DNA polymerase in pear SSR-PCR system were analyzed by quadratic regressive orthogonal rotational combinational design. Results showed： absolute IOD （Integrated OD of each band） valu...Effects of Mg^2＋, NTPs and Taq DNA polymerase in pear SSR-PCR system were analyzed by quadratic regressive orthogonal rotational combinational design. Results showed： absolute IOD （Integrated OD of each band） value of target band reduced with concentration rising of Mg^2＋ and Taq DNA polymerase, but heightened with concentration rising of dNTPs. The decay rate of absolute IOD value increased progressively with rising Mg^2＋ concentration, decreased gradually with rising Taq DNA polymerase concentration; the rising speed would be slower than the dNTPs increase. Absolute IOD value would reduce with concentration rising of dNTPs at a low level of Mg^2＋ concentration. Conversely it would rise with the increase of dNTPs while high Mg^2＋ concentration. Absolute IOD value would generally rise with concentration rising of Taq DNA polymerase while low Mg^2＋ concentration. On the contrary it would reduce with concentration rising of Taq DNA polymerase while high Mg^2＋ concentration.展开更多
文摘Deoxyribenucleoside triphosphate (dNTP) pools were measured in normal BALB/c3T3 cells, transformation-treated cells and transformed cells with reverse-phase HPLC. The fluctuation of dNTP pools was similar after transformation treatment with alkylating mutagen glycidyl methacrylate(GMA) or Nmethyl- N'- nitro N- nitrosoguanidine (MNNG ). However,the gap between deoxyguanosine triphosphate + deoxyadenosine triphosphate (dGTP + dATP) pools and deoxythymidine triphosphate + deoxycytidine triphosphate (dTTP + dCTP) pools was greatly intensified. The measurements also indicated that the dNTP pools in transformed cells were quite different from those in normal cells. The results suggested that dNTP pools may play an important role in cell transformation
文摘The induced mutation frequency by alkylating mutagen glycldyl methacrylate (GMA) and N-methyl-N'- nitro- N-nitrosoguanidine (MNNG) was investigated with or without perturbation of deoxyribenucleoside triphosphate (dNTP)pools; the influence of short treatment at different concentrations of GMA or MNNG on dNTP pools was also explored. The results indicated that the induced mutation frequency increased greatly at high dosages of mutagen (GMA~ 64 μg/ml, MNNG~ 8 μg/ml) and the perturbation on dNTP pools was carried out before the treatment of mutagen; the short treatment with mutagen could induce distinct fluctuations of dNTP pools, but different mutagen might have different effects on dNTP pools.According to the results of the present study and other reports in literature, we conclude that dNTP pools may be the targets of alkylating mutagens and the fluctuations of dNTP pools are closely associated with mutagenesis
文摘Effects of Mg^2＋, NTPs and Taq DNA polymerase in pear SSR-PCR system were analyzed by quadratic regressive orthogonal rotational combinational design. Results showed： absolute IOD （Integrated OD of each band） value of target band reduced with concentration rising of Mg^2＋ and Taq DNA polymerase, but heightened with concentration rising of dNTPs. The decay rate of absolute IOD value increased progressively with rising Mg^2＋ concentration, decreased gradually with rising Taq DNA polymerase concentration; the rising speed would be slower than the dNTPs increase. Absolute IOD value would reduce with concentration rising of dNTPs at a low level of Mg^2＋ concentration. Conversely it would rise with the increase of dNTPs while high Mg^2＋ concentration. Absolute IOD value would generally rise with concentration rising of Taq DNA polymerase while low Mg^2＋ concentration. On the contrary it would reduce with concentration rising of Taq DNA polymerase while high Mg^2＋ concentration.
