Howard Hughes Medical Institute and Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 8109-1024, USA.
Cold Spring Harb Perspect Biol. 2010 Oct;2(10):a003574. doi: 10.1101/cshperspect.a003574. Epub 2010 Sep 15.
The hammerhead, hairpin, hepatitis delta virus (HDV), Varkud Satellite (VS), and glmS ribozymes catalyze sequence-specific intramolecular cleavage of RNA. They range between 50 and 150 nucleotides in length, and are known as the "small self-cleaving ribozymes." Except for the glmS ribozyme that functions as a riboswitch in Gram-positive bacteria, they were originally discovered as domains of satellite RNAs. However, recent studies show that several of them are broadly distributed in genomes of organisms from many phyla. Each of these ribozymes has a unique overall architecture and active site organization. Crystal structures have revealed how RNA active sites can bind preferentially to the transition state of a reaction, whereas mechanistic studies have shown that nucleobases can efficiently perform general acid-base and electrostatic catalysis. This versatility explains the abundance of ribozymes in contemporary organisms and also supports a role for catalytic RNAs early in evolution.
锤头、发夹、δ 肝炎病毒 (HDV)、Varkud 卫星 (VS) 和 glmS 核酶催化 RNA 的序列特异性分子内切割。它们的长度在 50 到 150 个核苷酸之间,被称为“小自我切割核酶”。除了在革兰氏阳性菌中作为核糖开关发挥作用的 glmS 核酶外,它们最初是作为卫星 RNA 的结构域被发现的。然而,最近的研究表明,其中有几个广泛分布在来自多个门的生物体的基因组中。这些核酶中的每一种都具有独特的整体结构和活性位点组织。晶体结构揭示了 RNA 活性位点如何能够优先结合反应的过渡态,而机制研究表明,核碱基可以有效地进行一般酸-碱和静电催化。这种多功能性解释了当代生物体中核酶的丰富性,也支持了催化 RNA 在进化早期的作用。