Watson M A, Chaconas G
Department of Biochemistry, University of Western Ontario, Canada.
Cell. 1996 May 3;85(3):435-45. doi: 10.1016/s0092-8674(00)81121-6.
The chemical steps of bacteriophage Mu DNA transposition take place within a higher order nucleoprotein structure. We describe a novel intermediate that precedes the previously characterized transpososomes and directly demonstrates the interaction of a distant enhancer element with recombination regions. The transpositional enhancer interacts with the Mu left and right ends to form a three-site synaptic (LER) complex. Under normal reaction conditions, the LER complex is rapidly converted into the more stable Mu transpososomes. However, mutation of the Mu terminal nucleotides results in accumulation of the LER and a failure to form the type 0 transpososome. During the transition from LER to type 0, the Mu DNA termini and the active site of the transposase engage in a catalytically competent conformation.
噬菌体Mu DNA转座的化学步骤发生在一个高阶核蛋白结构内。我们描述了一种新的中间体,它先于先前表征的转座体,并直接证明了一个远距离增强子元件与重组区域的相互作用。转座增强子与Mu的左端和右端相互作用,形成一个三位突触(LER)复合体。在正常反应条件下,LER复合体迅速转化为更稳定的Mu转座体。然而,Mu末端核苷酸的突变导致LER的积累以及无法形成0型转座体。在从LER向0型转变的过程中,Mu DNA末端和转座酶的活性位点形成一种具有催化活性的构象。