Baldrich Patricia, Kakar Klementina, Siré Christelle, Moreno Ana Beatriz, Berger Angélique, García-Chapa Meritxell, López-Moya Juan José, Riechmann José Luis, San Segundo Blanca
Centre for Research in Agricultural Genomics (CRAG) CSIC-IRTA-UAB-UB, Edifici CRAG, Campus UAB, Bellaterra (Cerdanyola del Vallés), 08193 Barcelona, Spain.
BMC Genomics. 2014 Dec 10;15(1):1083. doi: 10.1186/1471-2164-15-1083.
Small RNAs (sRNAs), including small interfering RNAs (siRNAs) and microRNAs (miRNAs), have emerged as important regulators of eukaryotic gene expression. In plants, miRNAs play critical roles in development, nutrient homeostasis and abiotic stress responses. Accumulating evidence also reveals that sRNAs are involved in plant immunity. Most studies on pathogen-regulated sRNAs have been conducted in Arabidopsis plants infected with the bacterial pathogen Pseudomonas syringae, or treated with the flagelin-derived elicitor peptide flg22 from P. syringae. This work investigates sRNAs that are regulated by elicitors from the fungus Fusarium oxysporum in Arabidopsis.
Microarray analysis revealed alterations on the accumulation of a set of sRNAs in response to elicitor treatment, including miRNAs and small RNA sequences derived from massively parallel signature sequencing. Among the elicitor-regulated miRNAs was miR168 which regulates ARGONAUTE1, the core component of the RNA-induced silencing complex involved in miRNA functioning. Promoter analysis in transgenic Arabidopsis plants revealed transcriptional activation of MIR168 by fungal elicitors. Furthermore, transgenic plants expressing a GFP-miR168 sensor gene confirmed that the elicitor-induced miR168 is active. MiR823, targeting Chromomethylase3 (CMT3) involved in RNA-directed DNA methylation (RdDM) was also found to be regulated by fungal elicitors. In addition to known miRNAs, microarray analysis allowed the identification of an elicitor-inducible small RNA that was incorrectly annotated as a miRNA. Studies on Arabidopsis mutants impaired in small RNA biogenesis demonstrated that this sRNA, is a heterochromatic-siRNA (hc-siRNA) named as siRNA415. Hc-siRNAs are known to be involved in RNA-directed DNA methylation (RdDM). SiRNA415 is detected in several plant species.
Results here presented support a transcriptional regulatory mechanism underlying MIR168 expression. This finding highlights the importance of miRNA functioning in adaptive processes of Arabidopsis plants to fungal infection. The results of this study also lay a foundation for the involvement of RdDM processes through the activity of siRNA415 and miR823 in mediating regulation of immune responses in Arabidopsis plants.
小RNA(sRNA),包括小干扰RNA(siRNA)和微小RNA(miRNA),已成为真核基因表达的重要调节因子。在植物中,miRNA在发育、营养稳态和非生物胁迫反应中发挥关键作用。越来越多的证据还表明,sRNA参与植物免疫。大多数关于病原体调控sRNA的研究是在感染细菌病原体丁香假单胞菌的拟南芥植物中进行的,或者是用来自丁香假单胞菌的鞭毛蛋白衍生激发肽flg22处理的。这项工作研究了拟南芥中受尖孢镰刀菌激发子调控的sRNA。
微阵列分析揭示了一组sRNA在激发子处理后的积累变化,包括miRNA和源自大规模平行签名测序的小RNA序列。在受激发子调控的miRNA中,miR168调控AGO1,AGO1是参与miRNA功能的RNA诱导沉默复合体的核心成分。对转基因拟南芥植物的启动子分析表明,真菌激发子可转录激活MIR168。此外,表达GFP-miR168传感器基因的转基因植物证实了激发子诱导的miR168具有活性。靶向参与RNA指导的DNA甲基化(RdDM)的甲基转移酶3(CMT3)的miR823也被发现受真菌激发子调控。除了已知的miRNA外,微阵列分析还鉴定出一种被错误注释为miRNA的激发子诱导型小RNA。对小RNA生物合成受损的拟南芥突变体的研究表明,这种sRNA是一种异染色质siRNA(hc-siRNA),命名为siRNA415。已知hc-siRNA参与RNA指导的DNA甲基化(RdDM)。在几种植物物种中都检测到了siRNA415。
本文的结果支持了MIR168表达的转录调控机制。这一发现突出了miRNA在拟南芥植物对真菌感染的适应性过程中的重要作用。本研究结果也为通过siRNA415和miR823的活性参与RdDM过程介导拟南芥植物免疫反应调控奠定了基础。