Lee Linda, Sadowski Paul D
Department of Medical Genetics and Microbiology, Faculty of Medicine, University of Toronto, 4284 Medical Science Building, Toronto, Ont., Canada M5S 1A.
J Mol Biol. 2003 Feb 14;326(2):397-412. doi: 10.1016/s0022-2836(02)01429-8.
Conservative site-specific recombinases of the integrase family carry out recombination via a Holliday intermediate. The Cre recombinase, a member of the integrase family, was previously shown to initiate recombination by cleaving and exchanging preferentially on the bottom strand of its loxP target sequence. We have confirmed this strand bias for an intermolecular recombination reaction that used wild-type loxP sites and Cre protein. We have examined the sequence determinants for this strand preference by selectively mutating the two asymmetric scissile base-pairs in the lox site (those immediately adjacent to the sites of cleavage by Cre). We found that the initial strand exchange occurs preferentially next to the scissile G residue. Resolution of the Holliday intermediate thus formed takes place preferentially next to the scissile A residue. Lys86, which contacts the scissile nucleotides in the Cre-lox crystal structures, was important for establishing the strand preference in the resolution of the loxP-Holliday intermediate, but not for the initiation of recombination between loxP sites.
整合酶家族的保守位点特异性重组酶通过霍利迪中间体进行重组。Cre重组酶是整合酶家族的成员,先前已表明它通过优先在其loxP靶序列的底部链上切割和交换来启动重组。我们已经证实了这种链偏好对于使用野生型loxP位点和Cre蛋白的分子间重组反应。我们通过选择性地突变lox位点中两个不对称的可切割碱基对(那些紧邻Cre切割位点的碱基对)来研究这种链偏好的序列决定因素。我们发现初始链交换优先发生在可切割的G残基旁边。由此形成的霍利迪中间体的拆分优先发生在可切割的A残基旁边。在Cre-lox晶体结构中与可切割核苷酸接触的Lys86对于在loxP-霍利迪中间体拆分中建立链偏好很重要,但对于loxP位点之间的重组起始并不重要。