水稻BWMK1互作基因的分离
DOI:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:

国家自然科学基金(30470990)、国家教育部博士点基金(20060537004)、湖南农业大学作物种质创新与资源利用重点实验室科学基金开放项目(10KFXM13


Identification of rice genes interacting with BWMK1
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    为探明BWMK1介导的信号传导途径,采用酵母双杂交系统,构建水稻稻瘟病菌诱导后的cDNA文库,以BWMK1为诱饵,对文库进行筛选,通过验证、测序和基因编码分析,获得了7个BWMK1互作基因BWIP1~ BWIP7,分别位于水稻基因组第12、2、3、10、6、4、5 染色体上;7个互作基因中,除BWIP2和BWIP7未找到同源编码蛋白外,其余5个基因BWIP1 编码硫甲基转运酶,BWIP3 编码磷酸肌醇合成酶,BWIP4编码磷转运蛋白,BWIP5编码WD40重复包含蛋白,BWIP6 编码N乙酰谷氨酸激酶。

    Abstract:

    The rice MAPK gene BWMK1 is transcriptionally activated by fungal pathogen infection and wounding and acts as a positive regulator in plant disease resistance signaling. To further understand the BWMK1-mediated molecular signaling regulating pathways, a yeast two-hybrid system using BWMK1 as a bait was used to screen BWMK1 interacting proteins, and 7 BWMK1 interacting protein encoding genes BWIP1BWIP7 were isolated, BWIP1BWIP7 were located on 12, 2, 3, 10, 6, 4, 5 chromosomes, respectively. Homologous coding proteins were found for each isolated gene except BWIP2 and BWIP7, which indicated that BWIP1, 3, 4, 5 and 6 respectively coded for 5-methyltetrahydropteroyltriglutamate-homocysteine S-methyltransferase, myo-inositol phosphate synthease, putative phosphate transporter, WD-40 repeat containing protein and N-acetyl glutamate kinase 2.

    参考文献
    相似文献
    引证文献
引用本文

潘素君.水稻BWMK1互作基因的分离[J].湖南农业大学学报:自然科学版,2011,37(5):494-496.

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2011-04-02
  • 最后修改日期:2011-04-02
  • 录用日期:2011-05-08
  • 在线发布日期: 2011-10-14
  • 出版日期:
文章二维码