Lab of Modern Biotechnology, School of Forestry and Landscape Architecture, Anhui Agricultural University, Hefei 230036, China.
Plant Cell Rep. 2012 Jul;31(7):1199-217. doi: 10.1007/s00299-012-1241-0. Epub 2012 Feb 28.
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, Cys₂His₂ or Cys₂HisCys. 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.
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.
WRKY 转录因子参与植物的多种生理和发育过程。它们的 N 端具有高度保守的 WRKYGQK 氨基酸序列,其后是新型锌指样基序 Cys₂His₂或 Cys₂HisCys。迄今为止,在许多草本物种中已经鉴定和表征了许多 WRKY 基因。在木本物种中调查和表征 WRKY 基因将有助于更好地理解该基因家族的进化过程和功能。在这项研究中,在最新的杨树木基因组序列中鉴定了 104 个杨树 WRKY 基因(PtWRKY)。根据它们的结构特征,预测成员被分为以前在水稻中定义的 I-III 组。此外,基因的染色体定位表明,在染色体 14 上的 2.3 Mb 区域可能存在 WRKY 基因热点。此外,大约 83%(104 个中的 86 个)WRKY 基因参与基因复制事件,包括 69%(29 个中的 29 个)基因对表现出片段复制。使用半定量 RT-PCR,研究了不同胁迫[冷、干旱、盐和水杨酸(SA)]下亚组 III 基因的表达模式。数据显示,这些基因对各种胁迫条件表现出不同的表达水平。表达分析表明,PtWRKY76 基因在 0.1 mM SA 或 25% PEG-6000 处理下显著诱导。本研究为进一步克隆特定功能基因提供了基础线索,并可应用于研究和应用。
本研究鉴定了 104 个杨树 WRKY 基因,并证实了染色体 14 上的 WRKY 基因热点。此外,半定量 RT-PCR 显示亚组 III 对各种胁迫有不同的反应。