Nethanel T, Kaufmann G
Department of Biochemistry, Tel Aviv University, Ramat Aviv, Israel.
J Virol. 1990 Dec;64(12):5912-8. doi: 10.1128/JVI.64.12.5912-5918.1990.
Agents discriminating between DNA polymerase alpha and DNA polymerases of class delta (polymerase delta or epsilon) were used to characterize steps in the synthesis of the lagging DNA strand of simian virus 40 during DNA replication in isolated nuclei. The synthesis of lagging-strand intermediates below 40 nucleotides, termed DNA primers (T. Nethanel, S. Reisfeld, G. Dinter-Gottlieb, and G. Kaufmann, J. Virol. 62:2867-2873, 1988), was selectively inhibited by butylphenyl dGTP or by neutralizing DNA polymerase alpha monoclonal antibodies. The synthesis of longer lagging chains of up to 250 nucleotides (Okazaki pieces) was affected to a lesser extent, possibly indirectly, by these agents. Aphidicolin, which inhibits both alpha- and delta-class enzymes, elicited the opposite pattern: DNA primers accumulated in its presence and were not converted into Okazaki pieces. These and previous data suggest that DNA polymerase alpha primase synthesizes DNA primers, whereas another DNA polymerase, presumably DNA polymerase delta or epsilon, mediates the conversion of DNA primers into Okazaki pieces.
利用能够区分DNA聚合酶α与δ类DNA聚合酶(聚合酶δ或ε)的试剂,对在分离细胞核的DNA复制过程中猿猴病毒40滞后DNA链合成步骤进行了表征。长度低于40个核苷酸的滞后链中间体(称为DNA引物,T. 内塔内尔、S. 赖斯费尔德、G. 丁特 - 戈特利布和G. 考夫曼,《病毒学杂志》62:2867 - 2873, 1988)的合成被丁基苯基dGTP或通过中和DNA聚合酶α单克隆抗体而选择性抑制。长达250个核苷酸的较长滞后链(冈崎片段)的合成受这些试剂的影响较小,可能是间接影响。抑制α类和δ类酶的阿非科林引发了相反的模式:在其存在下DNA引物积累,且未转化为冈崎片段。这些以及之前的数据表明,DNA聚合酶α引发酶合成DNA引物,而另一种DNA聚合酶,推测为DNA聚合酶δ或ε,介导DNA引物向冈崎片段的转化。