Doherty E A, Doudna J A
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520, USA.
Annu Rev Biophys Biomol Struct. 2001;30:457-75. doi: 10.1146/annurev.biophys.30.1.457.
The past few years have seen exciting advances in understanding the structure and function of catalytic RNA. Crystal structures of several ribozymes have provided detailed insight into the folds of RNA molecules. Models of other biologically important RNAs have been constructed based on structural, phylogenetic, and biochemical data. However, many questions regarding the catalytic mechanisms of ribozymes remain. This review compares the structures and possible catalytic mechanisms of four small self-cleaving RNAs: the hammerhead, hairpin, hepatitis delta virus, and in vitro-selected lead-dependent ribozymes. The organization of these small catalysts is contrasted to that of larger ribozymes, such as the group I intron.
在过去几年里,我们对催化性RNA的结构和功能的理解取得了令人兴奋的进展。几种核酶的晶体结构为RNA分子的折叠提供了详细的见解。基于结构、系统发育和生化数据构建了其他具有生物学重要性的RNA模型。然而,关于核酶催化机制的许多问题仍然存在。本综述比较了四种小的自我切割RNA:锤头状、发夹状、丁型肝炎病毒和体外筛选的铅依赖性核酶的结构和可能的催化机制。将这些小催化剂的结构与较大的核酶(如I组内含子)的结构进行了对比。