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RNA肿瘤病毒的RNA依赖性DNA聚合酶活性。I. 反应中DNA的直接影响。

RNA-dependent DNA polymerase activity of RNA tumor viruses. I. Directing influence of DNA in the reaction.

作者信息

Hurwitz J, Leis J P

出版信息

J Virol. 1972 Jan;9(1):116-29. doi: 10.1128/JVI.9.1.116-129.1972.

Abstract

The template requirements and deoxyribonucleic acid (DNA) products of the DNA polymerases isolated from Rauscher leukemia and avian myeloblastosis viruses have been examined. All DNA preparations or synthetic polydeoxynucleotides which are active as primers possess a duplex structure containing single-stranded regions with a 3'-hydroxyl terminus. Native DNA and fully single-stranded DNA are inactive; moreover, their activity is not enhanced by sonic oscillation or treatment with micrococcal nuclease, Neurospora nuclease, or low levels of deoxyribonuclease I. Poor DNA templates are activated by treatment with exonuclease III, large amounts of deoxyribonuclease I, or an endonuclease isolated from Rauscher viral preparations. In reactions primed with deoxyadenylate-deoxythymidylate copolymer, the product formed is covalently attached to primer strands, indicating that no new strands are initiated. DNA polymerase products formed with exonuclease III- or deoxyribonuclase I-treated DNA are duplex structures. Short single-stranded regions are completely filled in, whereas long single-stranded regions are only partly repaired. DNA preparations containing extensive single-stranded regions are poorly utilized as templates.

摘要

对从劳氏肉瘤病毒和禽成髓细胞瘤病毒中分离出的DNA聚合酶的模板要求和脱氧核糖核酸(DNA)产物进行了研究。所有作为引物具有活性的DNA制剂或合成聚脱氧核苷酸都具有双链结构,该双链结构包含带有3'-羟基末端的单链区域。天然DNA和完全单链的DNA无活性;此外,通过超声振荡或用微球菌核酸酶、粗糙脉孢菌核酸酶或低水平的脱氧核糖核酸酶I处理,它们的活性不会增强。通过用核酸外切酶III、大量的脱氧核糖核酸酶I或从劳氏病毒制剂中分离出的一种内切酶处理,可以激活较差的DNA模板。在用脱氧腺苷酸-脱氧胸苷酸共聚物引发的反应中,形成的产物与引物链共价连接,这表明没有新链起始。用核酸外切酶III或脱氧核糖核酸酶I处理的DNA形成的DNA聚合酶产物是双链结构。短的单链区域被完全填满,而长的单链区域仅被部分修复。含有大量单链区域的DNA制剂作为模板的利用率很低。

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DNA nucleotide sequence restricted by the RI endonuclease.受RI核酸内切酶限制的DNA核苷酸序列。
Proc Natl Acad Sci U S A. 1972 Nov;69(11):3448-52. doi: 10.1073/pnas.69.11.3448.

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