中国农业科技导报 ›› 2017, Vol. 19 ›› Issue (11): 15-21.DOI: 10.13304/j.nykjdb.2017.0200

• 生物技术 生命科学 • 上一篇    下一篇

海岛棉GbWRKY53基因的克隆与表达分析

李静1§,刘思敏1§,蔡丽静2,王昭玉1,董丽君1,刘建凤1,张书玲1*   

  1. 1.河北大学生命科学学院, 河北 保定 071002; 2.河北省承德市兴隆县农牧局, 河北 兴隆 0673000
  • 收稿日期:2017-04-07 修回日期:2017-07-19 出版日期:2017-11-15 发布日期:2017-12-14
  • 通讯作者: 张书玲,副教授,博士,研究方向为植物分子育种与改良。E-mail: zslhealth@126.com
  • 作者简介:§李静与刘思敏为本文共同第一作者。李静,硕士研究生,研究方向为植物分子育 种与改良。E-mail:1554221921@qq.com;刘思敏,本科生,研究方向为植物逆境胁 迫机制。E-mail: 975878751@qq.com。
  • 基金资助:
    河北省自然科学基金项目(C2015201227);河北大学自然科学研究计划项目 (2014-277)资助。

Cloning and Expression Analysis of GbWRKY53 in G. barbadense

LI Jing1§, LIU Simin1§, CAI Lijing2, WANG Zhaoyu1, DONG Lijun1, LIU Jianfeng1, ZHANG Shuling1*   

  1. 1.College of Life Science, Hebei University, Hebei Baoding 071002; 2.Xinglong County Agriculture and Animal Husbandry Bureau of Chengde City in Hebei Province, Hebei Chengde 067300, China
  • Received:2017-04-07 Revised:2017-07-19 Online:2017-11-15 Published:2017-12-14

摘要: 黄萎病被称为棉花的“癌症”,挖掘和鉴定抗病相关基因是棉花抗黄萎病分子育种 的基础。WRKY转录因子在植物对生物和非生物胁迫应答过程中起重要调控作用。从 高抗黄萎病品种海岛棉Pima90-53中克隆了WRKY转录因子GbWRKY53,其开放阅读框 (open reading frame, ORF)为999 bp,编码332 个氨基酸,含有1 个WRKY结构 域及HXC型锌指结构,属于WRKY转录因子家族的第Ⅲ组。基因结构分析表明, GbWRKY53基因有3 个外显子和2 个内含子。系统进化分析表明,GbWRKY53与雷蒙德 氏棉(Gossypiumr aimindii)GrWRKY53的亲缘关系最近。当黄萎病菌诱导后, GbWRKY53基因表达量呈先增加后降低的变化趋势,处理后12 h其表达量达到最大; 水杨酸(SA)诱导后,GbWRKY53表达量在8 h明显增加,且一直持续增高到24 h; 而茉莉酸甲酯(MeJA)诱导后,GbWRKY53表达量在12 h达到最高值随后下降,且其 表达水平明显低于同时间水杨酸诱导后的表达量。1-氨基环丙烷-1-羧酸(ACC)诱 导后,GbWRKY53基因表达量仅微量上调。由此推断,GbWRKY53基因可能参与了复杂 的植物信号途径并在棉花抗黄萎病菌胁迫应答中起重要作用。

关键词: 棉花, WRKY, 黄萎病, 基因克隆, 表达分析

Abstract: Verticillium wilt is known as cotton cancer. Identifying of disease resistance gene is the basis for cotton verticillium wilt resistant molecular breeding. WRKY transcription factors play important roles in regulating plant responses to various abiotic and biotic stresses. In this study, a WRKY transcription factor GbWRKY53 was cloned from sea island cotton Pima 90-53 with high resistance to verticillium wilt. Its open reading frame (ORF) was 999 bp, and encoded a putative WRKY group Ⅲ protein with 332 amino acids and contained one conserved WRKY domains and one HXC zinc finger structure. The gene structure analysis showed that GbWRKY53 contained 3 exons and 2 introns. Phylogenetic analysis showed that GbWRKY53 closed to GrWRKY53. The expression of GbWRKY53 gene increased firstly and then decreased, and the expression of 12 h was the highest after Verticillium dahliae treatment. The expression of GbWRKY53 increased significantly after SA induction for 8 h, and maintained at a high level to 24 h. After the induction of methyl jasmonate (MeJA), the expression of GbWRKY53 reached the maximum at 12 h and then decreased. The expression level of GbWRKY53 was significantly lower than that of salicylic acid at the same time. The expression of GbWRKY53 gene was only slightly increased after the induction of ACC. It could be concluded that GbWRKY53 gene involved in the complex plant signaling pathway, and played an important role in cotton stress response to Verticillium dahliae.

Key words: cotton, WRKY, verticillium wilt, gene clone, expression analysis