Wang Li-Xia, Wang Yong, Hu Yuan-Lei, Gao Yin, Lin Zhong-Ping
National Key Laboratory of Protein Engineering and Plant Molecular Biology of Peking University, Beijing 100871, China.
Sheng Wu Gong Cheng Xue Bao. 2002 Sep;18(5):531-5.
The Cre recombinase, an integrase from bacteriophage P1, catalyzes site-specific recombination between 34-bp repeats termed loxP sites, in the absence of any additional cofactors and energy. Mediated by Cre recombinase, specific DNA fragments can be excised, inversed or integrated depending on the orientation or position of loxP sites in vitro or in vivo. Because of its simplicity and high efficiency, Cre/loxP site-specific recombination system has been widely used in gene deletion and function identification, gene site-specific integration, gene trapping and chromosome engineering. It has been used as a useful tool for DNA recombination in transgenic yeast, plants, insects and mammals. Here progress in the study of the structure and function of Cre recombinase is discussed.
Cre重组酶是一种来自噬菌体P1的整合酶,在没有任何其他辅助因子和能量的情况下,催化34碱基对重复序列(称为loxP位点)之间的位点特异性重组。在Cre重组酶的介导下,特定的DNA片段可以根据loxP位点在体外或体内的方向或位置被切除、反转或整合。由于其简单性和高效性,Cre/loxP位点特异性重组系统已广泛应用于基因缺失和功能鉴定、基因位点特异性整合、基因捕获和染色体工程。它已成为转基因酵母、植物、昆虫和哺乳动物中DNA重组的有用工具。本文讨论了Cre重组酶结构和功能研究的进展。