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Insights into aluminum-tolerance pathways in Stylosanthes as revealed by RNA-Seq analysis

机译:RNA-Seq分析揭示了对戟花铝耐性途径的洞察

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摘要

Stylo has a great potential for Al3+ resistance in acidic soils through secretion of citrate from the roots. To get insight into the molecular mechanisms responsible, transcriptomic changes were investigated in the roots after treatment with T01 (−Al3+, pH6.0), T02 (−Al3+, pH4.3) and T03 (50 µM AlCl3, pH4.3). In total, 83,197 unigenes generated from 130,933 contigs were obtained. Of them, 282, 148 and 816 differentially expressed unigenes (DEGs) were revealed in T01_vs_T02, T02_vs_T03 and T01_vs_T03 comparison, respectively (FDR < 0.001, log2FC > 2). DEGs by Al3+ were related to G-proteins, diacyglycerol and inositol metabolism, calcium-signaling, transcription regulation, protein modification and transporters for detoxification of Al3+. Additionally, Al3+ facilitates citrate synthesis via modifying gene expression of pathways responsible for citrate metabolism. Overall, Al3+ resistance in stylo involves multiple strategies and enhancement of citrate anabolism. The Al3+ signal transmits through heterotrimeric G-proteins, phospholipase C, inositol triphosphate, diacylglycerol, Ca2+ and protein kinases, thereby activating transcription and anion channels in plasma membrane, and resulting in citrate secretion from stylo roots.
机译:Stylo通过从根部分泌柠檬酸盐,在酸性土壤中具有极强的抗Al 3 + 的潜力。为了深入了解负责的分子机制,研究了用T01(-Al 3 + ,pH6.0),T02(-Al 3 + ,pH4.3)和T03(50μMAlCl3,pH4.3)。总共获得130,933个重叠群产生的83​​,197个单基因。其中,分别在T01_vs_T02,T02_vs_T03和T01_vs_T03比较中显示了282、148和816个差异表达的单基因(DEG)(FDR <0.001,log2FC> 2)。 Al 3 + 的DEG与G蛋白,双甘油和肌醇代谢,钙信号传导,转录调控,蛋白修饰以及Al 3 + 的解毒转运蛋白有关。此外,Al 3 + 通过修饰负责柠檬酸盐代谢的途径的基因表达来促进柠檬酸盐的合成。总体而言,手写笔对Al 3 + 的抗性涉及多种策略和增强柠檬酸合成代谢。 Al 3 + 信号通过异源三聚体G蛋白,磷脂酶C,肌醇三磷酸酯,二酰基甘油,Ca 2 + 和蛋白激酶传递,从而激活质膜的转录和阴离子通道,并导致从茎根分泌柠檬酸盐。

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