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铝离子胁迫下大豆根尖柠檬酸的分泌及SGA1基因的表达
引用本文:杨列耿,杨曙,张永先,唐健,黎晓峰. 铝离子胁迫下大豆根尖柠檬酸的分泌及SGA1基因的表达[J]. 作物学报, 2015, 41(4): 666-670. DOI: 10.3724/SP.J.1006.2015.00666
作者姓名:杨列耿  杨曙  张永先  唐健  黎晓峰
作者单位:1广西优良用材林资源培育重点实验室 / 广西林业科学研究院, 广西南宁530002; 2广西大学 / 亚热带生物资源保护与利用国家重点实验室,广西南宁 530005
基金项目:国家重点基础研究发展计划(973计划)项目(2014CB138701);国家自然科学基金项目(30771287);广西优良用材林资源培育重点实验室开发课题基金(12A0202);教育部博士学科点专项科研资金(200805930008)资助
摘    要:为揭示铝离子诱导大豆根尖分泌有机酸的特点及介导有机酸分泌的信号途径,采用溶液培养试验方法调查Al Cl3对大豆品种(广州本地2号)根尖有机酸分泌及SGA1基因表达的影响。结果表明,Al Cl3胁迫下大豆活体根尖分泌柠檬酸,且分泌量随着铝浓度(25、50μmol L–1Al Cl3)和处理时间(2~12 h)的增加而增加;大豆根尖以模式II分泌柠檬酸,处理后的前4 h,分泌速率很低,其后显著提升;有机酸明显分泌的诱导期长达6 h;在50μmol L–1 Al Cl3的溶液中添加异三聚体G蛋白抑制剂百日咳毒素(200 ng m L–1),柠檬酸分泌减少38.7%。RT-PCR分析结果显示,Al Cl3溶液诱导大豆根尖SGA1基因的表达,其表达水平随着铝处理时间(0.5~12.0 h)的延长有提升的趋势,而诱导的SGA1基因表达明显早于有机酸开始分泌时间(6 h)。这些结果表明,铝离子诱导大豆根尖分泌柠檬酸及SGA1基因的表达,异三聚体G蛋白可能作为铝胁迫信号开关器参与有机酸分泌的调控。

关 键 词:AlCl3  大豆  柠檬酸  异三聚体G蛋白  SGA1基因
收稿时间:2014-11-02

Secretion of Citrate from Root Apices and Expression of SGA1 in Soybean under AlCl3 Stress
YANG Lie-Geng;YANG Shu;ZHANG Yong-Xian;TANG Jian;LI Xiao-Feng. Secretion of Citrate from Root Apices and Expression of SGA1 in Soybean under AlCl3 Stress[J]. Acta Agronomica Sinica, 2015, 41(4): 666-670. DOI: 10.3724/SP.J.1006.2015.00666
Authors:YANG Lie-Geng  YANG Shu  ZHANG Yong-Xian  TANG Jian  LI Xiao-Feng
Affiliation:1.Guangxi Key Laboratory of Superior Timber Trees Resource Cultivation / Guangxi Forestry Research Institute, Nanning 530002, China;2.Guangxi University / State Key Laboratory for Conservation and Utilization of Subtropical Agrobioresources, Nanning 530004, China
Abstract:The effects of Al3+ on the secretion of organic acids from root apices and the expression of SGAI gene were investigated by hydroponics to elucidate the characteritics of organic acid secretion and Al3+ stress signal transduction pathway which mediates the secretion of organic acids in soybean Guangzhou 2. The results showed that soybean root apices (in vivo) secreted citrate under Al3+ stress. The secretion of citrate increased with the increase of Al3+ concentrations (25, 50 µmol L–1 AlCl3) and the prolongation (2–12 hours) of treatment with Al3+. Citrate was secreted from root apices by pattern II in soybean. The secretion rate was very low within initial four hours after Al3+ treatment but remarkably elevated thereafter. A gap of time between the secretion and Al3+ treatment reached to about six hours. On the other hand when cholera toxin, an inhibitor of heterotrimeric G-protein, was added to Al3+solution, the amount of citrate secreted decreased by 38.7%. RT-PCR analysis results indicated that Al3+ induced SGA1 expression. In general, the expression level was elevated with the prolongation of treatment with Al3+ (0.5 to 12 hours). Moreover, Al3+ induced expression of SGA1 sooner than the secretion of citrate. These results imply that Al3+ induces the secretion of citrate from root apices and SGA1 expression in the soybean, and heterotrimeric G proteins may act as a switch of Al3+ stress signal to be involved in the regulation of citrate secretion from root apices under Al3+ stress.
Keywords:AlCl3  Soybean  Citrate  Heterotrimeric G-protein  SGA1 gene
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