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多瘤病毒DNA在大肠杆菌中的分子克隆:仓鼠致癌性测试

Molecular cloning of polyoma virus DNA in Escherichia coli: oncogenicity testing in hamsters.

作者信息

Israel M A, Chan H W, Martin M A, Rowe W P

出版信息

Science. 1979 Sep 14;205(4411):1140-2. doi: 10.1126/science.224458.

Abstract

Inoculation of suckling hamsters with 2 x 10(8) live cells of Escherichia coli K12 strain chi1776, carrying the complete genome of polyoma virus in a recombinant plasmid, failed to induce tumors in any of 32 recipients. Also, lambda phage DNA and particles with a monomeric insert of polyoma DNA did not induce tumors. Purified recombinant plasmid DNA, as well as phage particles and DNA containing a head-to-tail dimer of polyoma DNA, showed a low degree of oncogenicity, comparable to that of polyoma DNA prepared from mouse cells. These findings support the previous conclusions, based on infectivity assays in mice, that propagation of polyoma virus DNA as a component of recombinant DNA molecules in E. coli K12 reduces its biologic activity many orders of magnitude relative to the virus itself.

摘要

用携带多瘤病毒完整基因组的重组质粒中的2×10⁸个大肠杆菌K12菌株chi1776的活细胞接种乳鼠,32只接种小鼠中无一诱发肿瘤。此外,λ噬菌体DNA以及带有多瘤病毒DNA单体插入片段的颗粒也不会诱发肿瘤。纯化的重组质粒DNA,以及含有多瘤病毒DNA头尾二聚体的噬菌体颗粒和DNA,显示出低程度的致癌性,与从小鼠细胞制备的多瘤病毒DNA相当。这些发现支持了先前基于小鼠感染性试验得出的结论,即多瘤病毒DNA作为重组DNA分子的一个组成部分在大肠杆菌K12中繁殖时,其生物学活性相对于病毒本身降低了许多个数量级。

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