Mizutani A, Temin H M
J Virol. 1975 Oct;16(4):797-806. doi: 10.1128/JVI.16.4.797-806.1975.
DNA polymerase was purified to apparent electrophoretic homogeneity from virions of spleen necrosis virus (SNV). (SNV is a member of the reticuloendotheliosis group of avian ribodeoxyviruses). The SNV DNA polymerase appears to consist of a single polypeptide with a molecular weight of 68,000. The SNV DNA polymerase has a preference for Mn2+ for DNA synthesis with an RNA template and Mg2+ for DNA synthesis with a deoxyribohomopolymer template. At the optimum concentrations of divalent cation, the relative rates of DNA synthesis by SNV DNA polymerase with different template.primers were similar to the relative rates of DNA synthesis by an avian leukosis virus DNA polymerase, with the exception of a lower relative rate of DNA synthesis by SNV DNA polymerase with SNV RNA. However, in contrast to DNA synthesized by the avian leukosis virus DNA polymerase with a SNV RNA template, DNA synthesized by SNV DNA polymerase with an SNV RNA template did not hybridize to the SNV RNA. SNV DNA polymerase has RNase H activity which is antigenically distinct from the RNase H activity of avian leukosis-sarcoma virus DNA polymerase.
从脾坏死病毒(SNV)的病毒粒子中纯化出了具有明显电泳均一性的DNA聚合酶。(SNV是禽核糖脱氧病毒网状内皮增生症组的成员之一)。SNV DNA聚合酶似乎由一条分子量为68,000的单一多肽组成。SNV DNA聚合酶在以RNA为模板进行DNA合成时优先选择Mn2+,而在以脱氧核糖同聚物为模板进行DNA合成时优先选择Mg2+。在二价阳离子的最佳浓度下,SNV DNA聚合酶与不同模板引物进行DNA合成的相对速率,与禽白血病病毒DNA聚合酶进行DNA合成的相对速率相似,但SNV DNA聚合酶以SNV RNA为模板进行DNA合成的相对速率较低。然而,与禽白血病病毒DNA聚合酶以SNV RNA为模板合成的DNA不同,SNV DNA聚合酶以SNV RNA为模板合成的DNA不能与SNV RNA杂交。SNV DNA聚合酶具有RNase H活性,该活性在抗原性上与禽白血病-肉瘤病毒DNA聚合酶的RNase H活性不同。