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1
Initiation by bacteriophage T1 of DNA packaging at a site between the P and Q genes of bacteriophage lambda.噬菌体T1在噬菌体λ的P基因和Q基因之间的位点启动DNA包装。
J Virol. 1984 Mar;49(3):754-9. doi: 10.1128/JVI.49.3.754-759.1984.
2
Phage T1-mediated transduction of a plasmid containing the T1 pac site.噬菌体T1介导的含有T1粘性末端位点的质粒转导。
J Mol Biol. 1986 Dec 20;192(4):681-92. doi: 10.1016/0022-2836(86)90021-5.
3
In vitro packaging into phage T4 particles and specific recircularization of phage lambda DNAs.噬菌体λDNA体外包装入T4噬菌体颗粒及特异性环化
Gene. 1986;46(1):97-101. doi: 10.1016/0378-1119(86)90171-x.
4
In vitro packaging of foreign DNA into heads of bacteriophage T1.将外源DNA体外包装到噬菌体T1的头部。
J Gen Virol. 1986 Feb;67 ( Pt 2):333-43. doi: 10.1099/0022-1317-67-2-333.
5
Identification of sequences necessary for packaging DNA into lambda phage heads.鉴定将DNA包装到λ噬菌体头部所需的序列。
Gene. 1982 Dec;20(2):267-79. doi: 10.1016/0378-1119(82)90045-2.
6
T1 pip: a mutant which affects packaging initiation and processive packaging of T1 DNA.T1 pip：一种影响T1 DNA包装起始和持续包装的突变体。
Virology. 1986 Apr 30;150(2):373-80. doi: 10.1016/0042-6822(86)90302-8.
7
Expression of the replication region of phage lambda DNA cloned into pBR322 in E. coli minicells.克隆到pBR322中的噬菌体λDNA复制区域在大肠杆菌微小细胞中的表达。
Acta Biochim Pol. 1982;29(3-4):227-33.
8
Selection of lambda Spi- transducing phages using the P2 old gene cloned onto a plasmid.使用克隆到质粒上的P2老基因来选择λ Spi - 转导噬菌体。
Gene. 1986;46(1):65-9. doi: 10.1016/0378-1119(86)90167-8.
9
A phage T4 in vitro packaging system for cloning long DNA molecules.一种用于克隆长DNA分子的噬菌体T4体外包装系统。
Gene. 1992 Apr 1;113(1):25-33. doi: 10.1016/0378-1119(92)90666-d.
10
Bacteriophage T7 DNA packaging. I. Plasmids containing a T7 replication origin and the T7 concatemer junction are packaged into transducing particles during phage infection.噬菌体T7 DNA包装。I. 在噬菌体感染期间，含有T7复制起点和T7多联体连接点的质粒被包装到转导颗粒中。
J Mol Biol. 1990 Dec 20;216(4):911-26. doi: 10.1016/S0022-2836(99)80010-2.

本文引用的文献

1
Sensitive mutants of bacteriophage lambda.噬菌体λ的敏感突变体
Virology. 1961 May;14:22-32. doi: 10.1016/0042-6822(61)90128-3.
2
Recombination between related temperate bacteriophages and the genetic control of immunity and prophage localization.相关温和噬菌体之间的重组以及免疫和原噬菌体定位的遗传控制。
Virology. 1957 Dec;4(3):509-21. doi: 10.1016/0042-6822(57)90083-1.
3
Genes of colliphage T1 whose products promote general recombination.其产物促进一般重组的大肠杆菌噬菌体T1的基因。
Virology. 1980 Sep;105(2):371-8.
4
Isolation and genetic characterization of T1-transducing mutants with increased transduction frequency.具有更高转导频率的T1转导突变体的分离与遗传特性分析
Virology. 1981 Jul 30;112(2):662-9. doi: 10.1016/0042-6822(81)90311-1.
5
T1 mutants with increased transduction frequency are defective in host chromosome degradation.转导频率增加的T1突变体在宿主染色体降解方面存在缺陷。
Virology. 1981 Jul 30;112(2):670-7. doi: 10.1016/0042-6822(81)90312-3.
6
A physical map of the permuted genome of bacteriophage T1.噬菌体T1重排基因组的物理图谱。
Mol Gen Genet. 1980;179(3):669-75. doi: 10.1007/BF00271756.
7
Deletion mutants of bacteriophage lambda. II. Genetic properties of att-defective mutants.噬菌体λ的缺失突变体。II. att缺陷型突变体的遗传特性。
J Mol Biol. 1971 Mar 14;56(2):385-401. doi: 10.1016/0022-2836(71)90472-4.
8
Studies of novel transducing variants of lambda: dispensability of genes N and Q.λ新型转导变体的研究：基因N和Q的非必需性
Virology. 1969 Oct;39(2):348-52. doi: 10.1016/0042-6822(69)90060-9.
9
Host specificity of DNA produced by Escherichia coli: bacterial mutations affecting the restriction and modification of DNA.大肠杆菌产生的DNA的宿主特异性：影响DNA限制与修饰的细菌突变
J Mol Biol. 1966 Mar;16(1):118-33. doi: 10.1016/s0022-2836(66)80267-x.
10
A deletion analysis of prophage lambda and adjacent genetic regions.噬菌体λ及相邻基因区域的缺失分析
Proc Natl Acad Sci U S A. 1968 Nov;61(3):956-62. doi: 10.1073/pnas.61.3.956.

噬菌体T1在噬菌体λ的P基因和Q基因之间的位点启动DNA包装。

Initiation by bacteriophage T1 of DNA packaging at a site between the P and Q genes of bacteriophage lambda.

作者信息

Drexler H

出版信息

J Virol. 1984 Mar;49(3):754-9. doi: 10.1128/JVI.49.3.754-759.1984.

DOI:10.1128/JVI.49.3.754-759.1984
PMID:6230461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC255534/
Abstract

The growth of phage T1 on cells tandemly lysogenic for heteroimmune lambdoid prophages leads to a nonrandom packaging of lambda DNA by T1. A site, called esp-lambda, is located between the P and Q genes of lambda and results in increased packaging to the left by T1. When cloned into pBR322, the esp-lambda site causes a significant increase in transduction of the plasmid by T1. The nin5 deletion inactivates esp-lambda.

摘要

噬菌体T1在对异源免疫性λ样原噬菌体呈串联溶原状态的细胞上生长，会导致T1对λDNA进行非随机包装。一个名为esp-λ的位点位于λ的P基因和Q基因之间，会导致T1向左的包装增加。当克隆到pBR322中时，esp-λ位点会使T1对该质粒的转导显著增加。nin5缺失会使esp-λ失活。