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Al-enhanced Expression and Interaction of 14-3-3 Protein and Plasma Membrane H+-ATPase is Related to Al-induced Citrate Secretion in an Al-resistant Black Soybean

机译:铝增强的表达和14-3-3蛋白与质膜H + -ATPase的相互作用与铝诱导的耐​​黑大豆铝诱导的柠檬酸盐分泌有关。

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The up-regulated expression of plasma membrane (PM) H+-ATPase is related to Al-enhanced citrate exudation in soybean. Moreover, the interaction with a 14-3-3 protein can activate PM H+-ATPase. This study investigated if the expression and interaction level of the 14-3-3 protein and PM H+-ATPase is associated with PM H+-ATPase activity as well as citrate secretion in Al-tolerant (RB) and Al-sensitive (SB) black soybeans, respectively, under 50 mM Al stress. The results showed that Al stress significantly induced transcription of the 14-3-3a gene in RB but not in SB roots. The Al-enhanced transcription of the PM H+-ATPase encoding gene (gha2) was higher in RB than in SB roots. The translation and phosphorylation of PM H+-ATPase, the interaction between the 14-3-3 protein and the phosphorylated PM H+-ATPase all showed an increasing pattern in RB but displayed a descending pattern in SB during the whole Al stress period. Consistently, H+ pump activity and citrate secretion were also higher in RB than in SB under Al stress. Furthermore, citrate secretion was correlated positively with PM H+-ATPase activity in RB and SB under Al stress. These results indicated that Al-enhanced expression of 14-3-3 protein and PM H+-ATPase and the interaction between 14-3-3 protein and phosphorylated PM H+-ATPase increased the activity of PM H+-ATPase and the H+ pump, thereby augmenting citrate secretion in RB. This might be an important molecular mechanism underlying the higher Al-tolerance in RB compared to SB.
机译:大豆质膜(PM)H + -ATPase的表达上调与铝增强柠檬酸盐​​的渗出有关。此外,与14-3-3蛋白的相互作用可以激活PM H + -ATPase。这项研究调查了14-3-3蛋白和PM H + -ATPase的表达和相互作用水平是否与耐铝(RB)和铝敏感(SB)黑中的PM H + -ATPase活性以及柠檬酸盐的分泌有关大豆分别在50 mM Al胁迫下。结果表明,铝胁迫显着诱导了RB根中14-3-3a基因的转录,而不是SB根中。 RB中PM H + -ATPase编码基因(gha2)的Al增强转录高于SB根。在整个Al胁迫期间,PM H + -ATPase的翻译和磷酸化,14-3-3蛋白与磷酸化的PM H + -ATPase的相互作用均显示RB呈增加模式,而SB呈下降模式。一致地,在铝胁迫下,RB中的H +泵活性和柠檬酸分泌也高于SB。此外,铝胁迫下RB和SB中柠檬酸的分泌与PM H + -ATPase活性呈正相关。这些结果表明,Al增强的14-3-3蛋白和PM H + -ATPase的表达以及14-3-3蛋白与磷酸化的PM H + -ATPase之间的相互作用增加了PM H + -ATPase和H +泵的活性,从而增加RB中柠檬酸盐的分泌。与SB相比,这可能是RB中较高的Al耐性的重要分子机制。

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