Genome-wide survey and characterization of the WRKY gene family in Populus trichocarpa

被引:231
|
作者
He, Hongsheng [1 ,2 ]
Dong, Qing [1 ]
Shao, Yuanhua [2 ]
Jiang, Haiyang [1 ]
Zhu, Suwen [1 ]
Cheng, Beijiu [1 ]
Xiang, Yan [1 ,2 ]
机构
[1] Anhui Agr Univ, Key Lab Biomass Improvement & Convers, Hefei 230036, Peoples R China
[2] Anhui Agr Univ, Lab Modern Biotechnol, Sch Forestry & Landscape Architecture, Hefei 230036, Peoples R China
关键词
WRKY; Poplar; Phylogenetic analysis; Duplication; Expression patterns; DNA-BINDING PROTEINS; TRANSCRIPTION FACTOR FAMILY; CDNA MICROARRAY; LEUCINE ZIPPER; ARABIDOPSIS; EXPRESSION; RICE; SUPERFAMILY; PATHOGEN; TOBACCO;
D O I
10.1007/s00299-012-1241-0
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
WRKY transcription factors participate in diverse physiological and developmental processes in plants. They have highly conserved WRKYGQK amino acid sequences in their N-termini, followed by the novel zinc-finger-like motifs, Cys(2)His(2) or Cys(2)HisCys. To date, numerous WRKY genes have been identified and characterized in a number of herbaceous species. Survey and characterization of WRKY genes in a ligneous species would facilitate a better understanding of the evolutionary processes and functions of this gene family. In this study, 104 poplar WRKY genes (PtWRKY) were identified in the latest poplar genome sequence. According to their structural features, the predicted members were divided into the previously defined groups I-III, as described in rice. In addition, chromosomal localization of the genes demonstrated that there might be WRKY gene hot spots in 2.3 Mb regions on chromosome 14. Furthermore, approximately 83% (86 out of 104) WRKY genes participated in gene duplication events, including 69% (29 out of 42) gene pairs which exhibited segmental duplication. Using semi-quantitative RT-PCR, the expression patterns of subgroup III genes were investigated under different stresses [cold, drought, salinity and salicylic acid (SA)]. The data revealed that these genes presented different expression levels in response to various stress conditions. Expression analysis exhibited PtWRKY76 gene induced markedly in 0.1 mM SA or 25% PEG-6000 treatment. The results presented here provide a fundamental clue for cloning specific function genes in further studies and applications. Key message This study identified 104 poplar WRKY genes and demonstrated WRKY gene hot spots on chromosome 14. Furthermore, semi-quantitative RT-PCR showed variable stress responses in subgroup III.
引用
收藏
页码:1199 / 1217
页数:19
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