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疏水表面诱导稻瘟病菌侵染结构发育过程的基因表达谱分析
引用本文:骆红梅,金庆超,彭友良,陈保善,李有志,邓烨,戴承恩,方永启,董海涛,李德葆.疏水表面诱导稻瘟病菌侵染结构发育过程的基因表达谱分析[J].农业生物技术学报,2007,15(6):1034-1041.
作者姓名:骆红梅  金庆超  彭友良  陈保善  李有志  邓烨  戴承恩  方永启  董海涛  李德葆
作者单位:1. 杭州师范大学生命与环境科学学院,杭州,310036
2. 浙江大学生物技术研究所,杭州,310029;浙江大学宁波理工学院生化分院,宁波,315100
3. 中国农业大学农业部分子植物病理学重点实验室,北京,100094
4. 广西大学亚热带生物资源保护和利用实验室,南宁,530004
5. 浙江大学生物技术研究所,杭州,310029
基金项目:国家高技术研究发展计划(863计划)
摘    要:本文在制备完成高通量稻瘟病菌cDNA阵列的基础上,平行检测孢子受疏水性表面诱导0、2、8、20和30 h时间点的基因表达谱。结果显示:在附着胞形成的不同阶段,均存在大量的差异表达基因,显示出这一过程中基因表达网络的复杂性。其中,附着胞在成熟阶段的差异表达基因数要明显高于其诱导和形成阶段,表现在8 h、20 h时间点相近的基因表达谱至30 h时间点发生剧烈变化。这种动态的基因表达谱的分析可以为稻瘟病菌致病的分子机理研究提供有意义的信息。

关 键 词:稻瘟病菌  附着胞  cDNA阵列  实时定量PCR
文章编号:1006-1304(2007)06-1034-08
收稿时间:2007-03-15
修稿时间:2007-04-07

Gene Expression Profile during the Development of Infecting Structures Induced by Hydrophobic Surfaces in Magnaporthe grisea
LUO Hong-mei,JIN Qing-chao,PENG You-liang,CHEN Bao-shan,LI You-zhi,DENG Ye,DAI Chen-gen,FANG Yong-qi,DONG Hai-tao,LI De-bao.Gene Expression Profile during the Development of Infecting Structures Induced by Hydrophobic Surfaces in Magnaporthe grisea[J].Journal of Agricultural Biotechnology,2007,15(6):1034-1041.
Authors:LUO Hong-mei  JIN Qing-chao  PENG You-liang  CHEN Bao-shan  LI You-zhi  DENG Ye  DAI Chen-gen  FANG Yong-qi  DONG Hai-tao  LI De-bao
Abstract:Gene expression profiles were monitored at 0, 2, 8, 20, and 30 h time points of development of the infection structures induced by hydrophobic surfaces with a cDNA array with 4 108 TUTs from Magnaphorthe grisea. The results showed that there were many differentially expressed genes which indicated a complexity of gene expression network at any time-points of appresorium development. More genes were differentially expressed during appressorium maturation than during appressorium induction and formation. That is to say, genes seemed to be most actively expressed during 20 to 30 h time-points. Therefore, a detailed and comprehensive analysis of the programmed gene expression that occurs during the continuous stages of appressorium development is necessary to better understand the pathogenesis of M. grisea.
Keywords:Magnaporthe grisea  appressorium  cDNA array  quantitative real-time PCR
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