Streicher B, Westhof E, Schroeder R
Institute of Microbiology and Genetics, Vienna Biocenter, Austria.
EMBO J. 1996 May 15;15(10):2556-64.
Several divalent metal ions (Ca2+, Sr2+ and Pb2+) do not promote splicing, but instead induce cleavage at a single site in the conserved group I intron core in the absence of the guanosine cofactor at elevated pH, generating products with 5'-OH and 3'-phosphate ends. The reaction is competed by Mg2+, which does not cleave at this position, but hydrolyses the splice sites producing 3'-OH and 5'-phosphate ends. Mn2+ promotes both core cleavage and splice site hydrolysis under identical conditions, suggesting that two different metal atoms are involved, each responsible for one type of cleavage, and with different chemical and geometric requirements. Based on the core cleavage position and on the previously proposed coordination sites for Mg2+, we propose a structural location for two metal ions surrounding the splice site in the Michel-Westhof three-dimensional model of the group I intron core. The proposed location was strengthened by a first mutational analysis which supported the suggested interaction between one of the metal ions and the bulged residue in P7.
几种二价金属离子(Ca2+、Sr2+和Pb2+)不会促进剪接,而是在pH升高且不存在鸟苷辅因子的情况下,诱导保守的I组内含子核心中的单个位点发生切割,产生具有5'-OH和3'-磷酸末端的产物。该反应受到Mg2+的竞争,Mg2+不会在该位置切割,而是水解剪接位点,产生3'-OH和5'-磷酸末端。在相同条件下,Mn2+既促进核心切割又促进剪接位点水解,这表明涉及两种不同的金属原子,每种金属原子负责一种类型的切割,并且具有不同的化学和几何要求。基于核心切割位置以及先前提出的Mg2+配位位点,我们在I组内含子核心的Michel-Westhof三维模型中提出了围绕剪接位点的两种金属离子的结构位置。首次突变分析支持了其中一种金属离子与P7中凸起残基之间的推测相互作用,从而加强了所提出的位置。