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手枪型自我切割核酶的生化分析

Biochemical analysis of pistol self-cleaving ribozymes.

作者信息

Harris Kimberly A, Lünse Christina E, Li Sanshu, Brewer Kenneth I, Breaker Ronald R

机构信息

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.

出版信息

RNA. 2015 Nov;21(11):1852-8. doi: 10.1261/rna.052514.115. Epub 2015 Sep 18.

Abstract

Pistol RNAs are members of a distinct class of self-cleaving ribozymes that was recently discovered by using a bioinformatics search strategy. Several hundred pistol ribozymes share a consensus sequence including 10 highly conserved nucleotides and many other modestly conserved nucleotides associated with specific secondary structure features, including three base-paired stems and a pseudoknot. A representative pistol ribozyme from the bacterium Lysinibacillus sphaericus was found to promote RNA strand scission with a rate constant of ∼10 min(-1) under physiological Mg(2+) and pH conditions. The reaction proceeds via the nucleophilic attack of a 2'-oxygen atom on the adjacent phosphorus center, and thus adheres to the same general catalytic mechanism of internal phosphoester transfer as found with all other classes of natural self-cleaving ribozymes discovered to date. Analyses of the kinetic characteristics and the metal ion requirements of the cleavage reaction reveal that members of this ribozyme class likely use several catalytic strategies to promote the rapid cleavage of RNA.

摘要

手枪状RNA是一类独特的自我切割核酶成员,最近通过生物信息学搜索策略被发现。数百种手枪状核酶共享一个共有序列,包括10个高度保守的核苷酸以及许多与特定二级结构特征相关的其他适度保守的核苷酸,这些特征包括三个碱基配对的茎和一个假结。在生理镁离子和pH条件下,发现来自球形赖氨酸芽孢杆菌的一种代表性手枪状核酶以约10分钟-1的速率常数促进RNA链断裂。该反应通过2'-氧原子对相邻磷中心的亲核攻击进行,因此遵循与迄今发现的所有其他天然自我切割核酶相同的内部磷酸酯转移一般催化机制。对切割反应的动力学特征和金属离子需求的分析表明,这类核酶成员可能使用多种催化策略来促进RNA的快速切割。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed8/4604425/c06aeaf9b820/1852F01.jpg

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