Gudima S O, Kazantseva E G, Kostyuk D A, Shchaveleva I L, Grishchenko O I, Memelova L V, Kochetkov S N
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 117984 Moscow, Russia.
Nucleic Acids Res. 1997 Nov 15;25(22):4614-8. doi: 10.1093/nar/25.22.4614.
Deoxyribonucleotide-containing RNA-like polynucleotides (dcRNAs) were synthesized by mutant T7 RNA polymerase and their structures confirmed by sequencing. dcRNAs annealed with a 20mer oligodeoxyribonucleotide primer were tested as templates/primers in the reverse transcription reaction catalyzed by HIV-1 reverse transcriptase (RT). All dcRNAs were shown to be efficient templates for both wild-type RT and RT mutants, containing 'AZT-resistant' mutations. Differences in the patterns of the DNA products of RNA- and dcRNA-driven reverse transcription were demonstrated. The kinetic characteristics for dcRNAs utilization were compared with the corresponding parameters for RNA/DNA and DNA/DNA templates/primers. The respective K m values for dcRNAs appear to be intermediate between those for RNA and DNA templates. A correlation equation connecting apparent K m value for template/primer and the number of deoxyribonucleotide substitutions in RNA template is proposed.
含脱氧核糖核苷酸的类RNA多核苷酸(dcRNAs)由突变型T7 RNA聚合酶合成,其结构通过测序得以确认。与20聚体寡脱氧核糖核苷酸引物退火的dcRNAs作为模板/引物,在由HIV-1逆转录酶(RT)催化的逆转录反应中进行测试。结果表明,所有dcRNAs对于野生型RT和含有“AZT抗性”突变的RT突变体而言都是有效的模板。研究证实了RNA驱动和dcRNA驱动的逆转录反应所产生的DNA产物模式存在差异。将dcRNAs利用的动力学特征与RNA/DNA和DNA/DNA模板/引物的相应参数进行了比较。dcRNAs各自的K m值似乎介于RNA和DNA模板的K m值之间。提出了一个将模板/引物的表观K m值与RNA模板中脱氧核糖核苷酸取代数联系起来的相关方程。