State Key Laboratory of Cotton Biology, Institute of Cotton Research of Chinese Academy of Agricultural Sciences, Key Laboratory for Cotton Genetic Improvement, Ministry of Agriculture, Anyang 455000, Henan, China.
Plant Sci. 2019 Mar;280:187-196. doi: 10.1016/j.plantsci.2018.11.015. Epub 2018 Nov 29.
Cotton production is severely constrained by drought, especially if encountered during the seedling stage or the fiber initiation and elongation stage, but the regulatory mechanisms underlying the effects of drought remain unclear. Therefore, characterization and functional analysis of microRNA-mediated stress regulatory networks are critical to deciphering plant drought response. In this study, 357, 379 and 377 miRNAs with annotations were obtained using the drought-resistant cotton variety ZhongH177 under three treatments, CK, drought and re-watering, and divided into 73 miRNA families with varying copy numbers from 1 to 24. 136 differential expressed genes (DEGs) with significant expression changes were found, of which only 33 DEGs were upregulated, while 103 DEGs were downregulated under drought stress. However, most DEGs recovered their initial expression states when the plants were re-watered. In total, 2657 targets were identified and found to be mainly enriched in the pathways plant-pathogen interaction, plant hormone signal transduction and biosynthesis of amino acids. Drought tolerance was significantly enhanced in 2 transgenic Arabidopsis lines, showing that miRNAs were involved in cotton drought response. Analysis of the expression patterns of 2 miRNA precursors and methylation alterations of 2 targets suggested that these miRNAs or miRNA precursors may be involved in the regulation of target methylation states. Our study provides evidence of transcriptional responses to drought stress, which will be helpful for the research of drought-resistance mechanisms in the future.
棉花生产受到干旱的严重限制,特别是在幼苗期或纤维起始和伸长期遇到干旱时,但干旱影响的调控机制仍不清楚。因此,对 miRNA 介导的应激调控网络的特征描述和功能分析对于破译植物的抗旱反应至关重要。在这项研究中,使用三个处理(CK、干旱和复水)下的抗旱棉花品种 ZhongH177 获得了 357、379 和 377 个具有注释的 miRNA,并将其分为 73 个 miRNA 家族,其拷贝数从 1 到 24 不等。发现了 136 个差异表达基因(DEGs),其表达变化显著,其中只有 33 个 DEGs 在干旱胁迫下上调,而 103 个 DEGs 下调。然而,当植物复水时,大多数 DEGs 恢复了其初始表达状态。总共鉴定了 2657 个靶标,发现它们主要富集在植物-病原体相互作用、植物激素信号转导和氨基酸生物合成途径中。2 个转基因拟南芥品系的耐旱性显著增强,表明 miRNAs 参与了棉花的抗旱反应。对 2 个 miRNA 前体的表达模式和 2 个靶标的甲基化改变分析表明,这些 miRNA 或 miRNA 前体可能参与了靶标甲基化状态的调控。我们的研究提供了对干旱胁迫转录反应的证据,这将有助于未来对抗旱机制的研究。