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首页> 外文期刊>Journal of Virology >Marek's Disease Herpesvirus-Induced DNA Polymerase
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Marek's Disease Herpesvirus-Induced DNA Polymerase

机译:Marek的疾病疱疹病毒诱导的DNA聚合酶

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Infection of duck embryo fibroblasts by Marek's disease herpesvirus (MDHV), strain GA, led to the induction of a novel DNA polymerase. This novel DNA polymerase, designated MDHV-induced DNA polymerase, could be distinguished from the DNA polymerase activities of uninfected duck embryo fibroblasts by its chromatographic behavior on phosphocellulose, by its sedimentation coefficient, and by its catalytic properties. The characteristics of MDHV-induced DNA polymerase which had been purified by phosphocellulose chromatography were investigated. The sedimentation coefficient of the enzyme, as determined by sucrose density gradient centrifugation in the presence of 0.25 M KCl, was 5.9S. From this sedimentation coefficient, the molecular weight of MDHV-induced DNA polymerase was estimated to be 100,000. MDHV-induced DNA polymerase could not effectively use either poly(dA)·oligo(dT)12-18 or poly(dC)·oligo(dG)12-18 as a template-primer. The DNA polymerases from uninfected duck embryo fibroblasts could use these synthetic template-primers. MDHV-induced DNA polymerase also could not use poly(rA)·oligo(dT)12-18 or poly(rC)·oligo(dG)12-18 as template-primers or oligo(dT)12-18 as a primer, indicating that it was not a polymerase of the type R-DNA polymerase, reverse transcriptase, or a terminal nucleotidyl transferase. In vitro synthesis of DNA by MDHV-induced DNA polymerase was markedly inhibited by the addition of (NH4)2SO4 to the reaction mixture.
机译:Marek疾病疱疹病毒(MDHV),应变Ga感染鸭胚胎成纤维细胞,导致了一种新型DNA聚合酶的诱导。该新型DNA聚合酶,指定的MDHV诱导的DNA聚合酶,可以通过其沉积系数的磷酸纤维素的色谱行为和其催化性能来区分除染鸭胚胎成纤维细胞的DNA聚合酶活性。研究了通过磷纤维素色谱纯化的MDHV诱导的DNA聚合酶的特性。通过在0.25M KCl存在下通过蔗糖密度梯度离心确定的酶的沉降系数为5.9 S 。从这种沉降系数来看,MDHV诱导的DNA聚合酶的分子量估计为100,000。 MDHV诱导的DNA聚合酶不能有效地使用聚(DA)·寡(DT)<亚> 12-18 或聚(DC)·寡(DG) 12-18 模板底漆。来自无感染的鸭胚成纤维细胞的DNA聚合酶可以使用这些合成模板引物。 MDHV诱导的DNA聚合酶也不能使用聚(Ra)·寡核苷酸(DT) 12-18 或聚(RC)·寡(DG) 12-18 作为模板 - 作为底漆的预期或寡聚(DT) 12-18 ,表明它不是R-DNA聚合酶,逆转录酶或末端核苷酸转移酶的聚合酶。通过加入(NH 4 2-4 通过加入(NH 4次>) 4-so>抑制DNA的体外合成DNA。 。

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