Manns A, König H, Baier M, Kurth R, Grosse F
Abteilung Chemie, Max-Planck-Institut für experimentelle Medizin, Göttingen, FRG.
Nucleic Acids Res. 1991 Feb 11;19(3):533-7. doi: 10.1093/nar/19.3.533.
The in vitro fidelity of highly purified recombinant reverse transcriptase from simian immunodeficiency virus of African green monkeys (SIVagm) was determined. By using the phi X174am16 reversion assay an overall error rate of 1/19,000 was determined. This is 2.4-fold higher than the overall accuracy of purified recombinant HIV-1 reverse transcriptase, measured in parallel. The evaluation of error frequencies from nucleotide pool bias studies suggest an even higher accuracy for the SIVagm-derived reverse transcriptase. T:dGMP mismatches were formed most frequently with an error rate of 1/155,000, followed by G:dGMP (1/230,000), A:dGMP (1/315,000), G:dAMP (1/340,000), T:dCMP (1/540,000), T:dTMP (1/790,000), and A:dCMP (1/1,050,000) mispairs. Thus, according to pool bias effects and depending on the mismatch under consideration SIVagm reverse transcriptase appears to be 2 to 20-fold more accurate than the homologous enzyme from the human immunodeficiency virus type 1. This higher accuracy is not due to a co-purifying exonuclaease activity. Like the enzyme from HIV-1, the simian monkey-derived enzyme was found to be devoid of a proofreading 3' to 5' exonuclease.
测定了来自非洲绿猴猿猴免疫缺陷病毒(SIVagm)的高度纯化重组逆转录酶的体外保真度。通过使用phi X174am16回复测定法,确定总体错误率为1/19,000。这比平行测量的纯化重组HIV-1逆转录酶的总体准确性高2.4倍。核苷酸库偏差研究中错误频率的评估表明,SIVagm衍生的逆转录酶具有更高的准确性。T:dGMP错配形成频率最高,错误率为1/155,000,其次是G:dGMP(1/230,000)、A:dGMP(1/315,000)、G:dAMP(1/340,000)、T:dCMP(1/540,000)、T:dTMP(1/790,000)和A:dCMP(1/1,050,000)错配。因此,根据库偏差效应并取决于所考虑的错配,SIVagm逆转录酶似乎比来自人类免疫缺陷病毒1型的同源酶准确2至20倍。这种更高的准确性并非由于共纯化的核酸外切酶活性。与HIV-1的酶一样,发现猿猴来源的酶缺乏3'至5'校对核酸外切酶。