Zhao Lei, Bonocora Richard P, Shub David A, Stoddard Barry L
Graduate Program in Molecular Biophysics, Structure and Design, University of Washington, Seattle, WA, USA.
EMBO J. 2007 May 2;26(9):2432-42. doi: 10.1038/sj.emboj.7601672. Epub 2007 Apr 5.
The homing endonuclease I-Ssp6803I causes the insertion of a group I intron into a bacterial tRNA gene-the only example of an invasive mobile intron within a bacterial genome. Using a computational fold prediction, mutagenic screen and crystal structure determination, we demonstrate that this protein is a tetrameric PD-(D/E)-XK endonuclease - a fold normally used to protect a bacterial genome from invading DNA through the action of restriction endonucleases. I-Ssp6803I uses its tetrameric assembly to promote recognition of a single long target site, whereas restriction endonuclease tetramers facilitate cooperative binding and cleavage of two short sites. The limited use of the PD-(D/E)-XK nucleases by mobile introns stands in contrast to their frequent use of LAGLIDADG and HNH endonucleases - which in turn, are rarely incorporated into restriction/modification systems.
归巢内切酶I-Ssp6803I可使一个I组内含子插入细菌的tRNA基因中,这是细菌基因组内侵入性移动内含子的唯一实例。通过计算折叠预测、诱变筛选和晶体结构测定,我们证明该蛋白质是一种四聚体PD-(D/E)-XK内切酶——这种折叠通常用于通过限制性内切酶的作用保护细菌基因组免受入侵DNA的影响。I-Ssp6803I利用其四聚体组装来促进对单个长靶位点的识别,而限制性内切酶四聚体则促进对两个短位点的协同结合和切割。移动内含子对PD-(D/E)-XK核酸酶的使用有限,这与它们频繁使用LAGLIDADG和HNH内切酶形成对比,而LAGLIDADG和HNH内切酶反过来很少被纳入限制/修饰系统。