Department of Computer Science and Engineering, Washington University in Saint Louis, Campus Box 1045, Saint Louis, MO 63130, USA.
Plant Mol Biol. 2011 Jan;75(1-2):93-105. doi: 10.1007/s11103-010-9710-8. Epub 2010 Dec 12.
MicroRNAs (miRNAs) are key regulators of gene expression in development and stress responses in most eukaryotes. We globally profiled plant miRNAs in response to infection of bacterial pathogen Pseudomonas syringae pv. tomato (Pst). We sequenced 13 small-RNA libraries constructed from Arabidopsis at 6 and 14 h post infection of non-pathogenic, virulent and avirulent strains of Pst. We identified 15, 27 and 20 miRNA families being differentially expressed upon Pst DC3000 hrcC, Pst DC3000 EV and Pst DC3000 avrRpt2 infections, respectively. In particular, a group of bacteria-regulated miRNAs targets protein-coding genes that are involved in plant hormone biosynthesis and signaling pathways, including those in auxin, abscisic acid, and jasmonic acid pathways. Our results suggest important roles of miRNAs in plant defense signaling by regulating and fine-tuning multiple plant hormone pathways. In addition, we compared the results from sequencing-based profiling of a small set of miRNAs with the results from small RNA Northern blot and that from miRNA quantitative RT-PCR. Our results showed that although the deep-sequencing profiling results are highly reproducible across technical and biological replicates, the results from deep sequencing may not always be consistent with the results from Northern blot or miRNA quantitative RT-PCR. We discussed the procedural differences between these techniques that may cause the inconsistency.
微小 RNA(miRNAs)是大多数真核生物发育和应激反应中基因表达的关键调节因子。我们对植物在感染细菌性病原菌丁香假单胞菌 pv.番茄(Pst)时的 miRNA 进行了全面分析。我们对拟南芥在感染非致病性、毒性和无毒菌株的 6 小时和 14 小时后构建的 13 个小 RNA 文库进行了测序。我们分别鉴定出了 15、27 和 20 个在 Pst DC3000 hrcC、Pst DC3000 EV 和 Pst DC3000 avrRpt2 感染时差异表达的 miRNA 家族。特别是,一组受细菌调控的 miRNA 靶向参与植物激素生物合成和信号通路的蛋白质编码基因,包括生长素、脱落酸和茉莉酸途径的基因。我们的结果表明,miRNAs 通过调节和微调多个植物激素途径,在植物防御信号中发挥重要作用。此外,我们将一小部分 miRNA 的测序分析结果与 miRNA Northern blot 和 miRNA 定量 RT-PCR 的结果进行了比较。我们的结果表明,尽管深度测序分析结果在技术和生物学重复中具有高度的可重复性,但深度测序的结果并不总是与 Northern blot 或 miRNA 定量 RT-PCR 的结果一致。我们讨论了这些技术之间可能导致不一致的程序差异。