Wang Chen, Fang Jinggui
College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China.
Methods Mol Biol. 2015;1296:109-18. doi: 10.1007/978-1-4939-2547-6_11.
Computational prediction of microRNAs (miRNAs) is one of the most important approaches in microRNA studies. While validation of the predicted microRNAs' precise sequences is essential for further studies on their biogenesis, evolution, and functions, computational miRNA prediction methods, however, often fail to predict the accurate sequence of the mature miRNA within the precursor at the nucleotide precision level. Here, we depict a highly efficient method for determining the precise sequences of computationally predicted miRNAs. The method combines the generation of miRNA-enriched libraries, with 5'- and 3'-end adaptors being linked to the miRNA molecules, the reverse transcription of small RNAs with an oligo-d(T) anchor primer, two specific 5'- and 3'-miRNA-RACE (miR-RACE) PCR reactions and sequence-directed cloning. The efficiency of this method was demonstrated by the precise sequence validation of computationally predicted miRNAs in citrus, apple, and other fruit crops. Our ongoing research indicates that miR-RACE is also very useful to verify the sequences of putative miRNAs obtained by deep sequencing of small RNA libraries. The protocol of miR-RACE is rapid and can be completed within 2-3 days. miR-RACE should make the bioinformatic prediction of miRNAs more powerful and accurate.
微小RNA(miRNA)的计算预测是miRNA研究中最重要的方法之一。虽然验证预测的微小RNA的精确序列对于进一步研究其生物发生、进化和功能至关重要,然而,计算miRNA预测方法往往无法在核苷酸精确水平上预测前体中成熟miRNA的准确序列。在此,我们描述了一种用于确定计算预测的miRNA精确序列的高效方法。该方法将富含miRNA的文库的构建、5'和3'末端接头与miRNA分子连接、用寡聚d(T)锚定引物对小RNA进行逆转录、两个特定的5'和3'miRNA-RACE(miR-RACE)PCR反应以及序列导向克隆相结合。通过对柑橘、苹果和其他水果作物中计算预测的miRNA进行精确序列验证,证明了该方法的有效性。我们正在进行的研究表明,miR-RACE对于验证通过小RNA文库深度测序获得的假定miRNA的序列也非常有用。miR-RACE方案快速,可在2-3天内完成。miR-RACE应使miRNA的生物信息学预测更强大、更准确。