植物学报 ›› 2014, Vol. 49 ›› Issue (2): 127-138.DOI: 10.3724/SP.J.1259.2014.00127

• 研究报告 •    下一篇

水稻病程相关PR1家族蛋白质在叶片生长及与白叶枯病菌互作反应中的表达

李雪姣, 范伟, 牛东东, 关明俐, 缪刘杨, 史佳楠, 窦世娟, 魏健, 刘丽娟, 李莉云, 刘国振*   

  1. 河北农业大学生命科学学院, 保定 071001
  • 收稿日期:2013-07-01 修回日期:2013-09-08 出版日期:2014-03-01 发布日期:2014-01-07
  • 通讯作者: 刘国振
  • 基金资助:

    国家自然科学基金

Expression Analysis of Pathogenesis-related 1 Proteins in Normal Growth of Rice Leaves and Interactions Between Rice and Xanthomonas oryzae pv. oryzae

Xuejiao Li, Wei Fan, Dongdong Niu, Mingli Guan, Liuyang Miao, Jianan Shi, Shijuan Dou, Jian Wei, Lijuan Liu, Liyun Li, Guozhen Liu*   

  1. College of Life Sciences, Hebei Agricultural University, Baoding 071001, China
  • Received:2013-07-01 Revised:2013-09-08 Online:2014-03-01 Published:2014-01-07
  • Contact: Guozhen Liu

摘要: 病程相关(PR)蛋白质经常被用作抗病反应的分子标记。利用免疫印迹(WB)技术检测了7个PR1家族蛋白质在水稻(Oryza sativa)叶片生长及与白叶枯病菌互作反应过程中的表达, 发现6个PR1家族蛋白质在叶片生长中有表达。检测PR1蛋白质在Xa21介导的抗白叶枯病过程中的表达, 结果显示PR1#052、PR1#072、PR1#073和PR1#121四个蛋白质在抗病反应后期呈上调或诱导表达, PR1#071则表达下调。进一步比较它们在抗病、感病和对照(Mock)反应中的表达丰度, 发现在抗病和感病反应中的变化幅度均明显大于对照反应, 推测这些PR蛋白质在水稻-白叶枯病菌互作反应中发挥作用。另外, 对PR1基因上游启动子区的cis元件进行了分析。该研究初步揭示了水稻PR1家族蛋白质的表达谱, 为进一步了解PR1蛋白质的功能提供了线索。

Abstract: Pathogenesis-related (PR) proteins are commonly used as markers of plant defense responses. To examine the expression patterns of rice PR proteins, we used western blot analysis to investigate rice PR1 family proteins and found 6 of 7 tested PR1 proteins expressed in rice leaves under normal growth. We examined the expression pattern of PR1 proteins in the interaction between rice and the bacterium Xanthomonas oryzae pv. oryzae (Xoo) and found PR1#052, PR1#072, PR1#073 and PR1#121 upregulated or induced in the later stage of Xa21-mediated incompatible interactions and PR1#071 downregulated. The comparison among resistance, susceptible and mock treatments demonstrated that the alteration in abundance was greater with resistance and susceptible than mock treatment, so PR1 proteins may play a role in rice under biotic stress. In addition, we predicted cis elements in the upstream promoter region of PR1 genes. We reveal the expression spectrum of rice PR1 family proteins and provide useful clues for the functional investigation of rice PR1 proteins.