内含子
核酶
RNA剪接
第二组内含子
第一组催化内含子
剪接体
哺乳动物CPEB3核酶
生物
外显子
核酶
剪接位点突变
遗传学
核糖核酸
化学
基因
作者
Mary R. Stahley,Scott A. Strobel
标识
DOI:10.1016/j.sbi.2006.04.005
摘要
The group I intron has served as a model for RNA catalysis since its discovery 25 years ago. Four recently determined high-resolution crystal structures complement extensive biochemical studies on this system. Structures of the Azoarcus, Tetrahymena and bacteriophage Twort group I introns mimic different states of the splicing or ribozyme reaction pathway and provide information on splice site selection and metal ion catalysis. The 5′-splice site is selected by formation of a conserved G·U wobble pair between the 5′-exon terminus and the intron. The 3′-splice site is identified through stacking of three base triples, in which the middle triple contains the conserved terminal nucleotide of the intron, ΩG. The structures support a two-metal-ion mechanism for group I intron splicing that might have corollaries to group II intron and pre-mRNA splicing by the spliceosome.
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