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    张玉, 张增林, 蒋彩虹, 常爱霞, 杨爱国, 罗成刚, 王绍美, 王元英. 烟草病程相关蛋白NtPR10基因克隆与表达分析[J]. 中国烟草科学, 2017, 38(3): 1-7. DOI: 10.13496/j.issn.1007-5119.2017.03.001
    引用本文: 张玉, 张增林, 蒋彩虹, 常爱霞, 杨爱国, 罗成刚, 王绍美, 王元英. 烟草病程相关蛋白NtPR10基因克隆与表达分析[J]. 中国烟草科学, 2017, 38(3): 1-7. DOI: 10.13496/j.issn.1007-5119.2017.03.001
    ZHANG Yu, ZHANG Zenglin, JIANG Caihong, CHANG Aixia, YANG Aiguo, LUO Chenggang, WANG Shaomei, WANG Yuanying. Cloning and Expression Analysis of a Pathogenesis Related Protein Gene NtPR10 in Tobacco (Nicotiana tabacum)[J]. CHINESE TOBACCO SCIENCE, 2017, 38(3): 1-7. DOI: 10.13496/j.issn.1007-5119.2017.03.001
    Citation: ZHANG Yu, ZHANG Zenglin, JIANG Caihong, CHANG Aixia, YANG Aiguo, LUO Chenggang, WANG Shaomei, WANG Yuanying. Cloning and Expression Analysis of a Pathogenesis Related Protein Gene NtPR10 in Tobacco (Nicotiana tabacum)[J]. CHINESE TOBACCO SCIENCE, 2017, 38(3): 1-7. DOI: 10.13496/j.issn.1007-5119.2017.03.001

    烟草病程相关蛋白NtPR10基因克隆与表达分析

    Cloning and Expression Analysis of a Pathogenesis Related Protein Gene NtPR10 in Tobacco (Nicotiana tabacum)

    • 摘要: 为鉴定烟草病程相关蛋白PR10的生物学功能,从普通烟草G28中克隆得到了NtPR10基因,基因全长483 bp,编码160个氨基酸。基因结构分析表明,该基因编码的蛋白包含病程相关蛋白家族Bet_v_I保守域,具有与核酸酶活性相关的“P-Loop”结构。利用TMHMM、SignalP、PrositeScan等软件分析发现,NtPR10不含跨膜区,无信号肽,有胞内定位特征。采用实时荧光定量PCR分别分析了TMV诱导下该基因在抗、感品种枯斑三生和G28中的表达模式。结果表明,在TMV诱导下,NtPR10基因在感病品种G28中显著上调表达;而在抗病品种枯斑三生中,TMV侵染后6 h,NtPR10基因显著上调表达,第12小时至第8天显著下调表达,而后至第16天逐渐升高至侵染前水平。综合以上结果,NtPR10应答了TMV侵染过程,并且在抗、感品种中整体呈现出相反的表达趋势,暗示了NtPR10在TMV侵染过程中具有重要功能,为深入分析NtPR10的抗病生物学功能奠定了基础。

       

      Abstract: In order to investigate the biological function of the tobacco pathogenesis-related protein PR10,NtPR10 gene was obtained from the tobacco variety G28,which is 483 bp in length,encoding 160 amino acids.The NtPR10 protein belongs to the pathogenesis related protein family containing the "Bet_v_I " domain and the " P-loop" domain which is related to nuclease activities.The bioinformatics analysis indicated that NtPR10 did not contain transmembrane region,no signal peptide,and exhibited intracellular localization features by TMHMM,SignalP and PrositeScan.The expression pattern of the gene in the resistant and susceptible cultivars was studied by RT-qPCR.The results showed that the NtPR10 gene was significantly up-regulated in the susceptible cultivar G28 after TMV treatment.While in resistant cultivar Sumsun NN,NtPR10 was up-regulated at 6 hours after TMV infection,and down-regulated between 12 hours and 8th day,and then increased gradually to the pre-infection level after 16th day.From above analysis,NtPR10 responses to TMV infection,and the expression trend is opposite in resistant and susceptible cultivars,suggesting that the NtPR10 might have an important function in the process of TMV infection.Results from this study provide the foundation for further analysis of the biological function of NtPR10.

       

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