Sandmeier H
Department of Preventive Dentistry and Oral Microbiology, University of Basel, Switzerland.
Mol Microbiol. 1994 May;12(3):343-50. doi: 10.1111/j.1365-2958.1994.tb01023.x.
Molecular analysis reveals a surprising sharing of short gene segments among a variety of large double-stranded DNA bacteriophages of enteric bacteria. Ancestral genomes from otherwise unrelated phages, including lambda, Mu, P1, P2 and T4, must have exchanged parts of their tail-fibre genes. Individual genes appear as mosaics with parts derived from a common gene pool. Therefore, horizontal gene transfer emerges as a major factor in the evolution of a specific part of phage genomes. Current concepts of homologous recombination cannot account for the formation of such chimeric genes and the recombinational mechanisms responsible are not known. However, recombination sites for DNA invertases and recombination site-like sequences are present at the boundaries of gene segments conferring the specificity for the host receptor. This, together with the properties of the DNA inversion mechanism, suggests that these site-specific recombination enzymes could be responsible for the exchange of host-range determinants.
分子分析显示,在多种肠道细菌的大型双链DNA噬菌体中,短基因片段存在惊人的共享现象。包括λ噬菌体、Mu噬菌体、P1噬菌体、P2噬菌体和T4噬菌体在内的原本不相关的噬菌体的祖先基因组,必定交换了它们尾丝基因的部分片段。单个基因呈现为镶嵌体,其部分片段源自一个共同的基因库。因此,水平基因转移成为噬菌体基因组特定部分进化的一个主要因素。同源重组的现有概念无法解释此类嵌合基因的形成,且负责的重组机制尚不清楚。然而,在赋予宿主受体特异性的基因片段边界处,存在DNA转化酶的重组位点和类似重组位点的序列。这一点,连同DNA倒位机制的特性,表明这些位点特异性重组酶可能负责宿主范围决定因素的交换。