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大肠杆菌噬菌体P1的遗传学研究。I. 利用原噬菌体缺失进行图谱绘制。

Genetic studies of coliphage P1. I. Mapping by use of prophage deletions.

作者信息

Walker D H, Walker J T

出版信息

J Virol. 1975 Sep;16(3):525-34. doi: 10.1128/JVI.16.3.525-534.1975.

Abstract

One hundred and ten amber mutants of coliphage P1 were isolated and localized into groups with respect to the existing genetic map by use of nonpermissive Escherichia coli K-12 strains lysogenic for P1 with deletions. These lysogens contain one of three types of deletion prophages: P1cry and its derivatives, P1dlacs, and P1dpros. Fourteen such lysogens were tested for their ability to rescue the amber mutants which were then assigned to one of nine deletion segments of the P1 genome defined by the termini of the various prophage deletions. The relationship of the nine deletion segments with the published P1 map is described, two new segments having been added. The deletions of the 14 prophages overlapped sufficiently to indicate that the P1 genetic prophage map should be represented in circular form, which is consistent with the fact that P1 is normally a circular plasmid in the prophage state. The distribution of mutants into deletion segments is nonrandom for at least one segment. In addition, the deletion termini of the 14 defective prophages coincided in five out of nine regions separating the nine deletion segments. Various possible explanations are discussed for the nonrandom recurrence of these deletion termini, including the evidence of hot spots of recombination.

摘要

分离出110个大肠杆菌噬菌体P1的琥珀突变体,并利用对P1具有溶原性且带有缺失的非允许性大肠杆菌K - 12菌株,根据现有的遗传图谱将它们分组。这些溶原菌含有三种类型的缺失原噬菌体之一:P1cry及其衍生物、P1dlacs和P1dpros。测试了14种这样的溶原菌拯救琥珀突变体的能力,然后将这些突变体分配到由各种原噬菌体缺失末端定义的P1基因组的9个缺失区段之一。描述了9个缺失区段与已发表的P1图谱的关系,其中增加了两个新的区段。14种原噬菌体的缺失有足够的重叠,表明P1遗传原噬菌体图谱应以环状形式表示,这与P1在原噬菌体状态下通常是环状质粒的事实一致。至少有一个区段的突变体在缺失区段中的分布是非随机的。此外,14个缺陷原噬菌体的缺失末端在分隔9个缺失区段的9个区域中的5个区域重合。讨论了这些缺失末端非随机重复出现的各种可能解释,包括重组热点的证据。

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