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质粒p15B的DNA倒位区域Min和噬菌体P1的Cin:噬菌体尾丝基因的进化

DNA inversion regions Min of plasmid p15B and Cin of bacteriophage P1: evolution of bacteriophage tail fiber genes.

作者信息

Sandmeier H, Iida S, Arber W

机构信息

Abteilung Mikrobiologie, Universität Basel, Switzerland.

出版信息

J Bacteriol. 1992 Jun;174(12):3936-44. doi: 10.1128/jb.174.12.3936-3944.1992.

DOI:10.1128/jb.174.12.3936-3944.1992
PMID:1534556
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC206102/
Abstract

Plasmid p15B and the genome of bacteriophage P1 are closely related, but their site-specific DNA inversion systems, Min and Cin, respectively, do not have strict structural homology. Rather, the complex Min system represents a substitution of a Cin-like system into an ancestral p15B genome. The substituting sequences of both the min recombinase gene and the multiple invertible DNA segments of p15B are, respectively, homologous to the pin recombinase gene and to part of the invertible DNA of the Pin system on the defective viral element e14 of Escherichia coli K-12. To map the sites of this substitution, the DNA sequence of a segment adjacent to the invertible segment in the P1 genome was determined. This, together with already available sequence data, indicated that both P1 and p15B had suffered various sequence acquisitions or deletions and sequence amplifications giving rise to mosaics of partially related repeated elements. Data base searches revealed segments of homology in the DNA inversion regions of p15B, e14, and P1 and in tail fiber genes of phages Mu, T4, P2, and lambda. This result suggest that the evolution of phage tail fiber genes involves horizontal gene transfer and that the Min and Pin regions encode tail fiber genes. A functional test proved that the p15B Min region carries a tail fiber operon and suggests that the alternative expression of six different gene variants by Min inversion offers extensive host range variation.

摘要

质粒p15B与噬菌体P1的基因组密切相关,但它们的位点特异性DNA倒转系统,即Min和Cin,分别没有严格的结构同源性。相反,复杂的Min系统代表了一个类似Cin的系统被替换到一个祖先p15B基因组中。p15B的min重组酶基因和多个可倒转DNA片段的替换序列,分别与大肠杆菌K-12缺陷病毒元件e14上Pin系统的pin重组酶基因和部分可倒转DNA同源。为了绘制这种替换的位点,测定了P1基因组中与可倒转片段相邻的一个片段的DNA序列。这与已有的序列数据一起表明,P1和p15B都经历了各种序列的获得或缺失以及序列扩增,从而产生了部分相关重复元件的镶嵌体。数据库搜索揭示了p15B、e14和P1的DNA倒转区域以及噬菌体Mu、T4、P2和λ的尾丝基因中的同源片段。这一结果表明噬菌体尾丝基因的进化涉及水平基因转移,并且Min和Pin区域编码尾丝基因。功能测试证明p15B的Min区域携带一个尾丝操纵子,并表明通过Min倒转对六种不同基因变体的交替表达提供了广泛的宿主范围变异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fee/206102/eb549d0d4b2b/jbacter00078-0112-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fee/206102/07ac0aa796d8/jbacter00078-0109-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fee/206102/eb549d0d4b2b/jbacter00078-0112-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fee/206102/07ac0aa796d8/jbacter00078-0109-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fee/206102/eb549d0d4b2b/jbacter00078-0112-a.jpg

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