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λ噬菌体粘性末端位点:导致对大肠杆菌整合宿主因子依赖的间隔/取代突变的分离

The bacteriophage lambda cohesive end site: isolation of spacing/substitution mutations that result in dependence on Escherichia coli integration host factor.

作者信息

Miller G, Feiss M

机构信息

Department of Microbiology, College of Medicine, University of Iowa, Iowa City 52242.

出版信息

Mol Gen Genet. 1988 Apr;212(1):157-65. doi: 10.1007/BF00322459.

DOI:10.1007/BF00322459
PMID:2836703
Abstract

Substitution, insertion and deletion mutations have been constructed at the XmnI restriction site in cos lambda. The XmnI site is located between cosB, the site where terminase binds lambda DNA; and cosN, the site where terminase introduces staggered nicks to generate cohesive ends. Substitution mutations and deletion of a base pair (a -1 change) do not obviously affect lambda growth and DNA packaging. Changes of -2, +2 and -3 render lambda unable to grow on host cells lacking integration host factor (IHF). The -3 mutant has a reduced burst size in IHF+ cells, due to a defect in the initiation of packaging. A -7 deletion mutation is lethal. Models for the basis of these mutational effects are discussed.

摘要

已在λ噬菌体的XmnI限制性位点构建了替换、插入和缺失突变。XmnI位点位于cosB(末端酶结合λDNA的位点)和cosN(末端酶引入交错切口以产生粘性末端的位点)之间。替换突变和一个碱基对的缺失(-1变化)不会明显影响λ噬菌体的生长和DNA包装。-2、+2和-3的变化使λ噬菌体在缺乏整合宿主因子(IHF)的宿主细胞上无法生长。-3突变体在IHF+细胞中的爆发量减少,这是由于包装起始存在缺陷。-7缺失突变是致死的。文中讨论了这些突变效应的基础模型。

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