刺葡萄抗白腐病转录因子VdWRKY53基因克隆及表达
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国家自然科学基金(31201599 ),国家葡萄产业技术体系(CARS-30),中国农业科学院科技创新工程专项经费(CAAS-ASTIP-2015-ZFRI)


Cloning and Expression of Transcription Factor VdWRKY53 in Vitis davidii
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    摘要:

    利用同源克隆的方法,分别获得‘刺葡萄0943’的转录因子VdWRKY53基因的编码区和启动子区域,分析其序列特征,通过实时荧光定量检测其对白腐病菌侵染和水杨酸诱导的反应,并以感病品种欧亚种‘黑比诺’为对照,分析不同种质中转录因子VdWRKY53基因序列及表达差异。结果表明:‘刺葡萄0943’的VdWRKY53基因,在其编码区和启动子区域都有抗病基因的序列和位点特征,在DNA和氨基酸水平上与‘黑比诺’VvWRKY53有5处差异,这5处氨基酸差异可能造成了其功能的差异;‘刺葡萄0943’和‘黑比诺’中的WRKY53基因启动子受葡萄白腐病菌和水杨酸诱导后表达量增加,且VdWRKY53基因表达量和趋势不同于‘黑比诺’VvWRKY53。生物信息学分析和实时荧光定量表明,在‘刺葡萄0943’抗病途径中VdWRKY53转录因子具有重要的生物学作用。

    Abstract:

    In order to clone VdWRKY53 transcription factor from ‘Vitis davidii 0943’,reveal the relationships between its sequence signature,gene function and the resistance to white rot fungi and reveal the molecular regulatory mechanisms of resistant germplasm preliminary,we designed primers and cloned VdWRY53 of ‘Vitis davidii 0943’ based on the known homologous sequences VvWRKY53.Its expression was verified through bioinformatic analysis of genes,promoters and real-time fluorescence quantitative PCR after inoculating white rot fungi and spraying salicylic acid.The expression of WRKY53 can be monitored in both ‘Vitis davidii 0943’ and ‘Pinot Noir’ grape which inoculate white rot fungi or salicylic acid by real-time fluorescence quantitative PCR verification.The CDS and promoter of the Chinese wild grape ‘Vitis davidii 0943’ VdWRKY53 both have the resistance genes feature.At the same time VdWRKY53 is different from the ‘Pinot Noir’ grape and the nucleic and animo acids are also different.These differences may cause different functions.VdWRKY53 plays an important biological function in grape disease resistance by bioinformatic analysis and real-time fluorescence quantitative PCR.

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冯虎,张颖,樊秀彩,等.刺葡萄抗白腐病转录因子VdWRKY53基因克隆及表达[J].西北植物学报,2015,35(8):1497-1505

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  • 在线发布日期: 2015-08-29
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