期刊文献+

棉花ERF-B3亚组转录因子基因GhERF5-3的克隆及表达 被引量:3

Cloning and Expression of Subgroup Transcription Factor Gene Gh ERF5-3of Cotton ERF-B3
原文传递
导出
摘要 植物在受到病原菌侵染时,ERF转录因子被诱导调控抗病相关基因的表达。为了研究棉花AP2/ERF-B3类转录因子在棉花抗病调控中的作用,用电子克隆及RT-PCR技术,从陆地棉抗枯萎品种‘中棉所12’根部c DNA克隆得到一个新的ERF转录因子Gh ERF5-3(登录号:MF197875)。利用q RT-PCR检测枯萎病及不同激素处理后该基因的表达。结果表明:其c DNA全长为672 bp,编码223个氨基酸,分子量24.95 k D,等电点为9.04,含有一个典型的保守AP2结构域,通过进化树分析属于B3亚组。枯萎病菌侵染后,随着侵染时间的延长,Gh ERF5-3基因呈现出先增后降的趋势,在24 h时间点,其相对表达量达到峰值;ET和Me JA处理后,Gh ERF5-3基因呈上调表达。SA处理后为下调表达。推断Gh ERF5-3基因响应枯萎病菌。 When plants are infected by pathogens, ERF transcription factors are induced to regulate the expression of disease resistance related genes. To investigate the role of cotton AP2/ERF-B3 transcription factors in cotton disease resistance regulation, a new ERF transcription factor named GhERF5-3 (accession number: MF197875) was cloned from the root cDNA of the "Zhong mian suo 12" by electronic cloning and RT-PCR technology. qRT-PCR was conducted to detect the expression of this gene after treatment of blight and different hormones. Results showed that the gene cDNA was of 672 bp, encoding 223 amino acids, with the molecular weight of 24.95 kD, and the isoelectric point of 9.04. It contained a typical conservative AP2 domain. Phylogenetic tree analysis showed that GhERF5-3 belonged to ERFB3 subgroup. After the infection of blight, with the extension of infection time, the GhERF5-3 gene showed the trend of first increasing and then decreasing, and the relative expression reached its peak at 24 h. After being treated by ET and MeJA, the expression level of GhERF5-3 gene increased. While its expression decreased after the SA treatment. Therefore, we speculated that GhERF5-3 genes might participate in the defense responses to blight.
出处 《分子植物育种》 CAS CSCD 北大核心 2018年第4期1050-1056,共7页 Molecular Plant Breeding
基金 国家自然基金项目(31260358)资助
关键词 棉花 ERF转录因子 枯萎病菌 基因克隆 基因表达 Cotton, ERF transcription factors, Blight, Gene cloning, Gene expression
  • 相关文献

参考文献10

二级参考文献119

  • 1刘建光,王永强,张寒霜,赵俊丽,郭娴,孟宪鹏.ERF转录因子在植物抗逆境胁迫的研究进展[J].华北农学报,2013,28(S1):214-218. 被引量:13
  • 2胡根海,喻树迅.利用改良的CTAB法提取棉花叶片总RNA[J].棉花学报,2007,19(1):69-70. 被引量:96
  • 3Guo H, Ecker JR. The ethylene signaling pathway: new in- sights. Curt Opin Plant Bio12004; 7:40-49. 被引量:1
  • 4Roman G, Lubarsky B, Kieber JJ, Rothenberg M, Ecker JR. Genetic analysis of ethylene signal transduction in Arabidop- sis thaliana: five novel mutant loci integrated into a stress response pathway. Genetics 1995; 139:1393-1409. 被引量:1
  • 5Alonso JM, Hirayama T, Roman G, Nourizadeh S, Ecker JR. EIN2, a bifunctional transducer of ethylene and stress respons- es in Arabidopsis. Science 1999; 284:2148-2152. 被引量:1
  • 6Bisson MM, Bleckmann A, Allekotte S, Groth G. EIN2, the central regulator of ethylene signalling, is localized at the ER membrane where it interacts with the ethylene receptor ETRI. Biochem J 2009; 424:1-6. 被引量:1
  • 7Chao Q, Rothenberg M, Solano R, Roman G, Terzaghi W, Ecker JR. Activation of the ethylene gas response pathway in Arabidopsis by the nuclear protein ETHYLENE-INSENSI- TIVE3 and related proteins. Cell 1997; 89:1133 - 1144. 被引量:1
  • 8An F, Zhao Q, Ji Y, et al. Ethylene-induced stabilization of ETHYLENE INSENSITIVE3 and EIN3-LIKEI is mediated by proteasomal degradation of EIN3 binding F-box 1 and 2 that requires EIN2 in Arabidopsis. Plant Cell 2010; 22:2384- 2401. 被引量:1
  • 9Cokol M, Nair R, Rost B, Finding nuclear localization signals, EMBO Rep 2000; 1:411-415. 被引量:1
  • 10Huang W, Perez-Garcia P, Pokhilko A, et al. Mapping the core of the Arabidopsis circadian clock defines the network struc- ture of the oscillator. Science 2012; 336:75-79. 被引量:1

共引文献82

同被引文献33

引证文献3

二级引证文献14

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部