Craig N L
Department of Microbiology and Immunology, George W. Hooper Foundation, University of California, San Francisco 94143.
Mol Microbiol. 1991 Nov;5(11):2569-73. doi: 10.1111/j.1365-2958.1991.tb01964.x.
The bacterial transposon Tn7 is an unusual mobile DNA segment. Most transposable elements move at low-frequency and display little target site-selectivity. By contrast, Tn7 inserts at high-frequency into a single specific site in the chromosomes of many bacteria. In the absence of this specific site, called attTn7 in Escherichia coli where Tn7 has been most extensively studied, Tn7 transposes at low-frequency and inserts into many different sites. Much has recently been learned about Tn7 transposition from both genetic and biochemical studies. The Tn7 recombination machinery is elaborate and includes a large number of Tn7-encoded proteins, probably host-encoded proteins and also rather large cis-acting transposition sequences at the transposon termini and at the target site. Dissection of the Tn7 transposition mechanism has revealed that the DNA strand breakage and joining reactions that underlie the translocation of Tn7 have several unusual features.
细菌转座子Tn7是一种不同寻常的可移动DNA片段。大多数转座元件以低频移动,并且几乎没有靶位点选择性。相比之下,Tn7能高频插入许多细菌染色体中的单个特定位点。在没有这个特定位点(在大肠杆菌中称为attTn7,对Tn7的研究最为广泛)的情况下,Tn7以低频转座并插入许多不同位点。最近,通过遗传学和生物化学研究,人们对Tn7转座有了很多了解。Tn7重组机制很复杂,包括大量由Tn7编码的蛋白质、可能还有宿主编码的蛋白质,以及转座子末端和靶位点处相当大的顺式作用转座序列。对Tn7转座机制的剖析表明,作为Tn7易位基础的DNA链断裂和连接反应有几个不同寻常的特征。