Department of Bioinformatics, College of Life Sciences, Zhejiang University, Zijingang Campus, Yu Hang Tang Road 388, Hangzhou 310058, PR China.
J Exp Bot. 2010 May;61(9):2271-80. doi: 10.1093/jxb/erq087. Epub 2010 Apr 13.
Since the beginning of this century, microRNAs (miRNAs), which are tiny RNA molecules, have become one of the major research topics on gene expression regulation in both animals and plants. The major task of miRNA study is to elucidate how the miRNAs are expressed in vivo, how they exert regulatory effects on their targets, and how they can be qualitatively or quantitatively cloned. For these purposes, the methodology of miRNA study has been developed and significantly improved in recent years. The focus here is on a number of powerful methods for plant miRNA research including bioinformatics tools and experimental approaches being used for upstream or downstream analysis of miRNAs or miRNA cloning. Some discrepancies exist in the miRNA research methodology between plants and animals, for example, 5' modified RACE (Rapid Amplification of cDNA Ends) can be used for cleavage target validation only in plants. However, numerous common methods are shared by these two miRNA research areas. Thus, this review will enhance our understanding of miRNA research methodology in organisms.
自本世纪初以来,微小 RNA(miRNAs)作为一种微小的 RNA 分子,已成为动植物基因表达调控研究的主要课题之一。miRNA 研究的主要任务是阐明 miRNA 如何在体内表达,它们如何对靶标发挥调节作用,以及如何对它们进行定性或定量克隆。为此,近年来 miRNA 研究的方法学得到了发展和显著改进。本文重点介绍了几种用于植物 miRNA 研究的强大方法,包括用于 miRNA 上游或下游分析或 miRNA 克隆的生物信息学工具和实验方法。植物和动物 miRNA 研究方法之间存在一些差异,例如,5' 修饰的 RACE(快速扩增 cDNA 末端)仅可用于植物的切割靶标验证。然而,这两个 miRNA 研究领域有许多共同的方法。因此,本文将增进我们对生物 miRNA 研究方法学的理解。