Li Sanshu, Lünse Christina E, Harris Kimberly A, Breaker Ronald R
Howard Hughes Medical Institute, Yale University, New Haven, Connecticut 06520-8103, USA Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520-8103, USA.
Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520-8103, USA.
RNA. 2015 Nov;21(11):1845-51. doi: 10.1261/rna.052522.115. Epub 2015 Sep 18.
Hatchet RNAs are members of a novel self-cleaving ribozyme class that was recently discovered by using a bioinformatics search strategy. The consensus sequence and secondary structure of this class includes 13 highly conserved and numerous other modestly conserved nucleotides interspersed among bulges linking four base-paired substructures. A representative hatchet ribozyme from a metagenomic source requires divalent ions such as Mg(2+) to promote RNA strand scission with a maximum rate constant of ∼4 min(-1). As with all other small self-cleaving ribozymes discovered to date, hatchet ribozymes employ a general mechanism for catalysis involving the nucleophilic attack of a ribose 2'-oxygen atom on an adjacent phosphorus center. Kinetic characteristics of the reaction demonstrate that members of this ribozyme class have an essential requirement for divalent metal ions and that they might have a complex active site that employs multiple catalytic strategies to accelerate RNA cleavage by internal phosphoester transfer.
短柄斧RNA是一类新型自我切割核酶的成员,该类核酶最近通过生物信息学搜索策略被发现。这类核酶的共有序列和二级结构包括13个高度保守的核苷酸以及许多其他适度保守的核苷酸,它们散布在连接四个碱基配对子结构的凸起之间。来自宏基因组来源的代表性短柄斧核酶需要二价离子(如Mg(2+))来促进RNA链断裂,最大速率常数约为4 min(-1)。与迄今发现的所有其他小型自我切割核酶一样,短柄斧核酶采用一种通用的催化机制,涉及核糖2'-氧原子对相邻磷中心的亲核攻击。该反应的动力学特征表明,这类核酶成员对二价金属离子有基本需求,并且它们可能有一个复杂的活性位点,采用多种催化策略通过内部磷酸酯转移加速RNA切割。