United States Department of Agriculture-Agricultural Research Service (USDA-ARS), Molecular Plant Pathology Laboratory, Beltsville, MD, USA.
Methods Mol Biol. 2022;2316:65-70. doi: 10.1007/978-1-0716-1464-8_6.
Protocols for extraction and purification of viroid RNAs from the tissues of infected herbaceous plant hosts are numerous. They range from lengthy, traditional protocols that require large amounts of starting tissue and take several days to perform to those based on column chromatography which is more efficient and can be performed with smaller amounts of infected tissue. The goal of all protocols is to enrich for RNA fractions that contain viroid RNAs, and the RNA extraction procedure is chosen and adjusted for the downstream method used for detection and characterization. Removal of inhibitors/impurities is generally not an issue for herbaceous hosts unless they contain and inordinate amounts of polysaccharides, tannins, and phenols. Subsequent purification of viroid circular and linear RNAs is performed using denaturing polyacrylamide gel electrophoresis. In this chapter, a specific method routinely used for viroid purification from herbaceous hosts and problems that may be encountered is described and is intended as a reference for beginners in the field.
从感染草本植物宿主组织中提取和纯化类病毒 RNA 的方案有很多。它们的范围从需要大量起始组织且需要数天才能完成的冗长的传统方案,到基于柱层析的方案不等,后者更有效,并且可以使用更少量的感染组织进行。所有方案的目标都是富集含有类病毒 RNA 的 RNA 级分,并且 RNA 提取程序是根据用于检测和表征的下游方法来选择和调整的。除非草本宿主含有异常大量的多糖、单宁和酚类物质,否则一般不会出现抑制剂/杂质去除的问题。类病毒环状和线性 RNA 的后续纯化是使用变性聚丙烯酰胺凝胶电泳进行的。在本章中,描述了一种从草本宿主中常规用于纯化类病毒的特定方法以及可能遇到的问题,旨在为该领域的初学者提供参考。