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园艺学报 ›› 2011, Vol. 38 ›› Issue (10): 1911-1920.

• 蔬菜 • 上一篇    下一篇

黄瓜根结RDR酶基因的分离与表达分析

张婧妹,茆振川,刘 峰,陈国华,杨宇红,冯东昕,谢丙炎*   

  1. (中国农业科学院蔬菜花卉研究所,农业部蔬菜种质遗传改良重点实验室,北京 100081)
  • 收稿日期:2011-06-27 修回日期:2011-09-20 出版日期:2011-10-25 发布日期:2011-10-25
  • 通讯作者: 谢丙炎*

Isolation and Expression Analysis of CsRDRs in Root-knot of Cucumis sativus

ZHANG Jing-mei,MAO Zhen-chuan,LIU Feng,CHEN Guo-hua,YANG Yu-hong,FENG Dong-xin,and XIE Bing-yan*   

  1. Institute of Vegetables and Flowers,Key Laboratory of the Ministry of Agriculture on Genetic Improvement for Vegetable Germplasm,Chinese Academy of Agricultural Sciences,Beijing 100081,China
  • Received:2011-06-27 Revised:2011-09-20 Online:2011-10-25 Published:2011-10-25
  • Contact: XIE Bing-yan

摘要: 基于黄瓜(Cucumis sativus L.)自交系9930全基因组序列,采用RT-PCR的方法,分离出根结形成过程中表达的RDR基因,共获得了5个CsRDR基因:CsRDR1a、CsRDR1b、CsRDR1c、CsRDR2和CsRDR6(HQ738485 ~ HQ738489)。qPCR定量分析表明,5个基因在接种根结线虫后的不同时期表达量都有不同程度的增加。CsRDR1a、CsRDR1b、CsRDR2和CsRDR6在接种线虫早期(6 h)相对表达量明显增加;而CsRDR1c在接种36 h时相对表达量达到最高,从而表明CsRDR基因与黄瓜根结的发育相关。

关键词: 黄瓜, 根结, RDR, 分离, 表达

Abstract: To indentify the RDR genes and their expression characteristics involved in the root-knot development of cucumber(Cucumis sativus L.),RT-PCR and qPCR approaches were used in this study. Five CsRDR genes were isolated from root-knot of cucumber via RT-PCR,including CsRDR1a,CsRDR1b,CsRDR1c,CsRDR2 and CsRDR6(GenBank No. HQ738485–HQ738489). qPCR analysis showed that the expression of five CsRDR genes were increased at different levels in different stages upon Meloidogyne incognita infection. CsRDR1a,CsRDR1b,CsRDR2 and CsRDR6 displayed a significant increase in expression at the early stage(6 hours after M. incognita infection),while the expression of CsRDR1c was enhanced at 36 hours after the inoculation. The results revealed that CsRDR genes were related to the root-knot development of Cucumis sativus,which laid a foundation for the prevention of root-knot nematode through molecular breeding technology.

Key words: Cucumis sativus, root-knot, RDR, isolation, expression

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