Li Kuiyin, Liu Xiaojuan, He Fang, Chen Songshu, Zhou Guangyi, Wang Yuhai, Li Luhua, Zhang Suqin, Ren Mingjian, Yuan Yuanyuan
Guizhou Subcenter of National Wheat Improvement Center, College of Agronomy, Guizhou University, Guiyang, China.
Anshun University, Anshun, China.
Front Plant Sci. 2022 Dec 14;13:1042078. doi: 10.3389/fpls.2022.1042078. eCollection 2022.
The transcription factor WRKY is widespread in the plant kingdom and plays a crucial role in diverse abiotic stress responses in plant species. Tritipyrum, an octoploid derived from an intergeneric cross between Triticum aestivum (AABBDD) and Thinopyrum elongatum (EE), is a valuable germplasm resource for introducing superior traits of Th. elongatum into T. aestivum. The recent release of the complete genome sequences of T. aestivum and Th. elongatum enabled us to investigate the organization and expression profiling of Tritipyrum WRKY genes across the entire genome.
In this study, 346 WRKY genes, from TtWRKY1 to TtWRKY346, were identified in Tritipyrum. The phylogenetic analysis grouped these genes into three subfamilies (I-III), and members of the same subfamilies shared a conserved motif composition. The 346 TtWRKY genes were dispersed unevenly across 28 chromosomes, with 218 duplicates. Analysis of synteny suggests that the WRKY gene family may have a common ancestor. Expression profiles derived from transcriptome data and qPCR demonstrated that 54 TtWRKY genes exhibited relatively high levels of expression across various salt stresses and recovery treatments. Tel1E01T143800 (TtWRKY256) is extremely sensitive to salt stress and is on the same evolutionary branch as the salt-tolerant A. thaliana genes AtWRKY25 and AtWRKY33. From 'Y1805', the novel AtWRKY25 was cloned. The Pearson correlation analysis identified 181 genes that were positively correlated (R>0.9) with the expression of TtWRKY256, and these genes were mainly enriched in metabolic processes, cellular processes, response to stimulus, biological regulation, and regulation of biological. Subcellular localization and qRT-PCR analysis revealed that TtWRKY256 was located in the nucleus and was highly expressed in roots, stems, and leaves under salt stress.
The above results suggest that TtWRKY256 may be associated with salt stress tolerance in plants and may be a valuable alien gene for improving salt tolerance in wheat.
转录因子WRKY在植物界广泛存在,在植物物种对多种非生物胁迫的响应中发挥关键作用。八倍体小偃麦(Tritipyrum)由普通小麦(Triticum aestivum,AABBDD)和长穗偃麦草(Thinopyrum elongatum,EE)属间杂交产生,是将长穗偃麦草优良性状导入普通小麦的宝贵种质资源。普通小麦和长穗偃麦草完整基因组序列的近期公布,使我们能够研究小偃麦WRKY基因在全基因组中的组织和表达谱。
在本研究中,从小偃麦中鉴定出346个WRKY基因,命名为TtWRKY1至TtWRKY346。系统发育分析将这些基因分为三个亚家族(I - III),同一亚家族的成员具有保守的基序组成。346个TtWRKY基因不均匀地分布在28条染色体上,其中有218个重复基因。共线性分析表明WRKY基因家族可能有一个共同祖先。转录组数据和qPCR的表达谱显示,54个TtWRKY基因在各种盐胁迫和恢复处理中表现出相对较高的表达水平。Tel1E01T143800(TtWRKY256)对盐胁迫极为敏感,与耐盐拟南芥基因AtWRKY25和AtWRKY33处于同一进化分支。从‘Y1805’中克隆了新的AtWRKY25。Pearson相关性分析确定了181个与TtWRKY256表达呈正相关(R>0.9)的基因,这些基因主要富集在代谢过程、细胞过程、对刺激的反应、生物调控和生物学调节方面。亚细胞定位和qRT - PCR分析表明,TtWRKY256位于细胞核中,在盐胁迫下根、茎和叶中高表达。
上述结果表明,TtWRKY256可能与植物耐盐性相关,可能是提高小麦耐盐性的有价值的外源基因。