Jawaharlal Nehru Tropical Botanic Garden and Research Institute (JNTBGRI), Palode, Thiruvananthapuram, India.
Department of Botany, University of Kerala, Thiruvananthapuram, India.
Plant Biol (Stuttg). 2019 Jan;21(1):3-14. doi: 10.1111/plb.12888. Epub 2018 Sep 6.
Cardamom has long been used as a food flavouring agent and in ayurvedic medicines for mouth ulcers, digestive problems and even depression. Extensive occurrence of pests and diseases adversely affect its cultivation and result in substantial reductions in total production and productivity. Numerous studies revealed the significant role of miRNAs in plant biotic stress responses. In the current study, miRNA profiling of cultivar and wild cardamom genotypes was performed using an Ion Proton sequencer. We identified 161 potential miRNAs representing 42 families, including monocot/tissue-specific and 14 novel miRNAs in both genotypes. Significant differences in miRNA family abundance between the libraries were observed in read frequencies. A total of 19 miRNAs (from known miRNAs) displayed a twofold difference in expression between wild and cultivar genotypes. We found 1168 unique potential targets for 40 known miRNA families in wild and 1025 potential targets for 42 known miRNA families in cultivar genotypes. The differential expression analysis revealed that most miRNAs identified were highly expressed in cultivars and, furthermore, lower expression of miR169 and higher expression of miR529 in wild cardamom proved evidence that wild genotypes have stronger drought stress tolerance and floral development than cultivars. Potential targets predicted for the newly identified miRNAs from the miRNA libraries of wild and cultivar cardamom genotypes involved in metabolic and developmental processes and in response to various stimuli. qRT-PCR confirmed miRNAs were differentially expressed between wild and cultivar genotypes. Furthermore, four target genes were validated experimentally to confirm miRNA-mRNA target pairing using RNA ligase-mediated 5' Rapid Amplification of cDNA Ends (5'RLM-RACE) PCR.
小豆蔻长期以来一直被用作食品调味剂和阿育吠陀医学中的口腔溃疡、消化问题甚至抑郁症的药物。害虫和疾病的广泛发生对其种植产生不利影响,导致总产量和生产力大幅下降。许多研究表明,miRNA 在植物生物胁迫反应中发挥着重要作用。在本研究中,使用 Ion Proton 测序仪对栽培和野生小豆蔻基因型进行了 miRNA 图谱分析。我们在两种基因型中鉴定了 161 个代表 42 个家族的潜在 miRNA,包括单子叶植物/组织特异性和 14 个新 miRNA。在读取频率上观察到文库之间 miRNA 家族丰度的显著差异。在野生和栽培基因型之间,有 19 个 miRNA(来自已知 miRNA)的表达差异为两倍。我们发现野生和栽培基因型中 40 个已知 miRNA 家族的 1168 个潜在靶标和 42 个已知 miRNA 家族的 1025 个潜在靶标。差异表达分析表明,鉴定出的大多数 miRNA 在栽培品种中高度表达,此外,野生小豆蔻中 miR169 的表达降低和 miR529 的表达升高证明了野生基因型比栽培品种具有更强的耐旱性和花发育能力。预测来源于野生和栽培小豆蔻基因型 miRNA 文库的新 miRNA 的潜在靶标参与代谢和发育过程,并对各种刺激作出反应。qRT-PCR 证实了 miRNA 在野生和栽培基因型之间存在差异表达。此外,使用 RNA 连接酶介导的 5'快速扩增 cDNA 末端(5'RLM-RACE)PCR 实验验证了四个靶基因,以确认 miRNA-mRNA 靶标配对。