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拟南芥电压依赖型阴离子通道参与水杨酸信号应答
引用本文:文国琴,柴靓,刘震,李德款,罗勤,李旭锋,王健美,杨毅.拟南芥电压依赖型阴离子通道参与水杨酸信号应答[J].中国农业科技导报,2011,13(3):35-40.
作者姓名:文国琴  柴靓  刘震  李德款  罗勤  李旭锋  王健美  杨毅
作者单位:(1.四川大学生命科学院, 生物资源与生态环境教育部重点实验室, 水力学与山区河流开发保护国家重点实验室, 成都 610064,2.西华师范大学生命科学院, 四川 南充 637002)
摘    要:电压依赖型阴离子通道蛋白(voltage-dependent anion channels, VDAC)是线粒体外膜分布的重要蛋白,参与形成线粒体通透性转换孔,控制线粒体内外的物质进出。以RLD拟南芥为材料,构建VDAC过量表达和抑制表达的转基因株系,初步探索VDAC在水杨酸(Salicylic acid, SA)信号传递途径中的作用。对转基因拟南芥种子进行SA处理的萌发实验,发现VDAC影响拟南芥种子对SA的敏感性:过量表达株系种子对SA敏感,萌发率较低,而抑制表达株系种子敏感性较低,萌发率高。用实时荧光定量PCR检测SA信号传递的Marker基因PR1,发现在过量表达株系中,伴随VDAC水平升高,PR1上调;同样在抑制表达株系中,VDAC降低,PR1下降。由此说明,VDAC参与了拟南芥SA信号传递。

关 键 词:拟南芥  电压依赖型阴离子通道  水杨酸  信号传递  

Voltage-dependent Anion Channels of Arabidopsis thaliana Involved in Salicylic Acid Signaling Pathway
WEN Guo-qin,CHAI Liang,LIU Zhen,LI De-kuan,LUO Qin,LI Xu-feng,WANG Jian-mei,YANG Yi.Voltage-dependent Anion Channels of Arabidopsis thaliana Involved in Salicylic Acid Signaling Pathway[J].Journal of Agricultural Science and Technology,2011,13(3):35-40.
Authors:WEN Guo-qin  CHAI Liang  LIU Zhen  LI De-kuan  LUO Qin  LI Xu-feng  WANG Jian-mei  YANG Yi
Institution:(1.Key Laboratory of Bio-resources and Eco-environment, Ministry of Education, College of Life Science, State Key Laboratory of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu 610064|2. College of Life Science, China West Normal University, Sichuan Nanchong 637002, China)
Abstract:Voltage-dependent anion channels (VDAC) proteins distribute in mitochondrial outer membrane. They participate in the formation of mitochondrial permeability transition pore (PTP) and control substances in and out of the mitochondria. To explore the possibility of VDAC in SA signaling pathway, Arabidopsis thaliana (RLD) was taken as experiment material, and transgenic plant lines of VDAC over-expression and inhibited expression were gotten. Then germination experiment of transgenic plant seeds were treated with SA. The result showed that VDAC affected the sensitivity to SA of transgenic seeds. The over-expression lines seeds were sensitive to SA, with low germination rate. In contrast, the inhibited expression lines were less sensitive and the germination rate was high. PR1, marker gene of SA signaling pathway, was used for the real-time fluorescence quantitative PCR. It was found that in over-expression lines, accompanied by VDAC high level, PR1 increased; and in the inhibition lines, VDAC lower level, PR1 declined. In summary, Arabidopsis thaliana VDAC was involved in SA signaling pathway.
Keywords:Arabidopsis thaliana  voltage-dependent anion channels(VDAC)  SA  signaling pathway  
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