Burke J M, Berzal-Herranz A
Department of Microbiology and Molecular Genetics, Markey Center for Molecular Genetics, University of Vermont, Burlington 05405.
FASEB J. 1993 Jan;7(1):106-12. doi: 10.1096/fasebj.7.1.8422956.
In vitro selection and in vitro evolution methods represent powerful tools for isolating functional RNA molecules, and are proving to have wide applications in biology. Selection in the absence of living cells is possible because some RNA molecules possess a selectable "phenotype" (catalytic activity or ligand binding) as well as a "genotype" (nucleotide sequence). This review discusses the basic principles of in vitro selection technology and the application of these methods to isolate RNA molecules with interesting and novel properties. Selection techniques have been used to analyze the structure and function of catalytic RNA molecules (ribozymes), and to isolate novel catalytic structures not found in nature. They are also useful for studying protein-RNA interactions and for isolating RNA molecules that bind specifically to peptides and other ligands. The isolation of RNA molecules with new binding functionalities (aptamers) for both large and small molecules has exciting potential for discovery of new drugs and diagnostic reagents.
体外筛选和体外进化方法是分离功能性RNA分子的强大工具,并且已证明在生物学中具有广泛应用。在没有活细胞的情况下进行筛选是可行的,因为一些RNA分子既具有可选择的“表型”(催化活性或配体结合)又具有“基因型”(核苷酸序列)。本综述讨论了体外筛选技术的基本原理以及这些方法在分离具有有趣和新颖特性的RNA分子中的应用。筛选技术已被用于分析催化RNA分子(核酶)的结构和功能,并分离自然界中未发现的新型催化结构。它们也有助于研究蛋白质-RNA相互作用以及分离与肽和其他配体特异性结合的RNA分子。分离对大分子和小分子均具有新结合功能的RNA分子(适体)对于发现新药和诊断试剂具有令人兴奋的潜力。