National Key Laboratory of Crop Genetic Improvement and National Center of Plant Gene Research (Wuhan), Huazhong Agricultural University, Wuhan 430070, China.
Mol Genet Genomics. 2010 Dec;284(6):477-88. doi: 10.1007/s00438-010-0581-0. Epub 2010 Oct 13.
MicroRNAs are a class of endogenous small RNA molecules (20-24 nucleotides) that have pivotal roles in regulating gene expression mostly at posttranscriptional levels in plants. Plant microRNAs have been implicated in the regulation of diverse biological processes including growth and stress responses. However, the information about microRNAs in regulating abiotic stress responses in rice is limited. We optimized a one-tube stem-loop reverse transcription quantitative PCR (ST-RT qPCR) for high-throughput expression profiling analysis of microRNAs in rice under normal and stress conditions. The optimized ST-RT qPCR method was as accurate as small RNA gel blotting and was more convenient and time-saving than other methods in quantifying microRNAs. With this method, 41 rice microRNAs were quantified for their relative expression levels after drought, salt, cold, and abscisic acid (ABA) treatments. Thirty-two microRNAs showed induced or suppressed expression after stress or ABA treatment. Further analysis suggested that stress-responsive cis-elements were enriched in the promoters of stress-responsive microRNA genes. The expressions of five and seven microRNAs were significantly affected in the rice plant with defects in stress tolerance regulatory genes OsSKIPa and OsbZIP23, respectively. Some of the predicted target genes of these microRNAs were also related to abiotic stresses. We conclude that ST-RT qPCR is an efficient and reliable method for expression profiling of microRNAs and a significant portion of rice microRNAs participate in abiotic stress response and regulation.
microRNAs 是一类内源性的小 RNA 分子(20-24 个核苷酸),在植物中主要在转录后水平上发挥调控基因表达的关键作用。植物 microRNAs 参与了多种生物学过程的调节,包括生长和应激反应。然而,关于 microRNAs 在调控水稻非生物胁迫反应中的信息是有限的。我们优化了一种单管茎环反转录定量 PCR(ST-RT qPCR)方法,用于高通量分析正常和胁迫条件下水稻中 microRNAs 的表达谱。优化后的 ST-RT qPCR 方法与小 RNA 凝胶印迹一样准确,并且比其他方法更方便、更省时,可用于定量 microRNAs。使用该方法,对干旱、盐、冷和脱落酸(ABA)处理后 41 个水稻 microRNAs 的相对表达水平进行了定量。32 个 microRNAs 在应激或 ABA 处理后表现出诱导或抑制表达。进一步分析表明,应激响应顺式元件在应激响应 microRNA 基因的启动子中富集。在应激耐受调节基因 OsSKIPa 和 OsbZIP23 缺陷的水稻植株中,五个和七个 microRNAs 的表达分别受到显著影响。这些 microRNAs 的一些预测靶基因也与非生物胁迫有关。我们得出结论,ST-RT qPCR 是一种高效可靠的 microRNAs 表达谱分析方法,水稻中相当一部分 microRNAs 参与了非生物胁迫反应和调节。