Gottfried P, Yagil E, Kolot M
Department of Biochemistry, The George S. Wise Center for Life Sciences, Tel-Aviv University, Israel.
Mol Gen Genet. 2000 May;263(4):619-24. doi: 10.1007/s004380051209.
The site-specific recombination systems of bacteriophages lambda and HK022 share the same mechanism and their integrase proteins show strong homology. Nevertheless the integrase protein of each phage can only catalyze recombination between its own att sites. Previous work has shown that the specificity determinants in the att sites are located within the sequences that bind the integrase to the core of att. DNA fragments that carry attL and attR sites of each phage were challenged with each of the two integrases and the DNA-protein complexes were examined by the gel-retardation technique. The results show that each integrase can form higher-order DNA-protein complexes only with its cognate att sites, suggesting that differences in the mode of binding to the core are responsible for the specificity difference between the two integrases.
噬菌体λ和HK022的位点特异性重组系统具有相同的机制,且它们的整合酶蛋白表现出很强的同源性。然而,每个噬菌体的整合酶蛋白只能催化其自身附着位点之间的重组。先前的研究表明,附着位点中的特异性决定因素位于将整合酶与附着位点核心结合的序列内。携带每个噬菌体附着位点L和附着位点R的DNA片段分别用两种整合酶中的每一种进行处理,并用凝胶阻滞技术检测DNA-蛋白质复合物。结果表明,每种整合酶只能与其同源的附着位点形成高阶DNA-蛋白质复合物,这表明与核心结合模式的差异是两种整合酶之间特异性差异的原因。