首页> 外文期刊>Indian Journal of Biochemistry & Biophysics >GbWRKY1, a novel cotton (Gossypium barbadense) WRKY gene isolated from a bacteriophage full-length cDNA library, is induced by infection with Verticillium dahliae
【24h】

GbWRKY1, a novel cotton (Gossypium barbadense) WRKY gene isolated from a bacteriophage full-length cDNA library, is induced by infection with Verticillium dahliae

机译:GbWRKY1 是一种从棉花噬菌体全长cDNA文库中分离的新型棉花(Gossypium barbadense )WRKY基因,是通过感染黄萎病菌诱导的

获取原文
           

摘要

WRKY transcription factor proteins play important roles in diverse stress responses. In this study, we first cloned a novel WRKY from our constructed bacteriophage full-length cDNA library for cotton (Gossypium barbadense). The plants were stressed by exposure to a defoliating strain of Verticillium dahliae. The capacity of primary cDNA library was 1.28 × 106 PFU and the titer of the amplified cDNA library was 1010 PFU mL–1. The recombination rate of the library was 94% and average insert size was about 1.1 kb. This novel gene, named GbWRKY1 was 1971 bp long and encodes a protein of 489 amino acids. It contains two characteristic WRKY domains and two zinc finger motifs. The sub-cellular assay indicated that GbWRKY1–GFP fusion protein was localized in the nucleus. Furthermore, Northern blot analysis showed that expression pattern of GbWRKY1 was similar among tissue types (roots, stems and leaves), but differed between pathogen-infiltrated and Czapek medium-infiltrated (untreated control) plants. Quantitative real-time PCR showed that GbWRKY1 could also be induced by salicylic acid (SA), methyl jasmonate (MeJA) and 1-aminocyclopropane-1-carboxylic acid (ACC). These findings clearly suggest that as a pathogen-inducible transcription factor GbWRKY1 plays an important role in plant defense responses.
机译:WRKY转录因子蛋白在多种应激反应中起重要作用。在这项研究中,我们首先从我们构建的棉花噬菌体全长cDNA文库中克隆了一种新型WRKY(棉花棒)。通过暴露于黄萎病菌的去叶菌株对植物施加压力。初级cDNA文库的容量为1.28×106 PFU,扩增的cDNA文库的滴度为> 1010 PFU mL-1。文库的重组率为94%,平均插入片段大小为1.1 kb。这个名为GbWRKY1的新基因长1971 bp,编码489个氨基酸。它包含两个特征性的WRKY域和两个锌指基序。亚细胞分析表明,GbWRKY1-GFP融合蛋白位于细胞核中。此外,Northern印迹分析表明,GbWRKY1的表达模式在组织类型(根,茎和叶)之间相似,但在病原体浸润和Czapek培养基浸润(未经处理的对照)植物之间却有所不同。实时定量PCR表明,水杨酸(SA),茉莉酸甲酯(MeJA)和1-氨基环丙烷-1-羧酸(ACC)也可以诱导GbWRKY1。这些发现清楚地表明,作为病原体诱导的转录因子,GbWRKY1在植物防御反应中起着重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号