Zhang Liyuan, Gu Lingkun, Ringler Patricia, Smith Stanley, Rushton Paul J, Shen Qingxi J
School of Life Sciences, University of Nevada, Las Vegas, NV 89154, USA.
Texas A&M AgriLife Research and Extension Center, Dallas, TX 75252, USA.
Plant Sci. 2015 Jul;236:214-22. doi: 10.1016/j.plantsci.2015.04.014. Epub 2015 Apr 24.
Members of the WRKY transcription factor superfamily are essential for the regulation of many plant pathways. Functional redundancy due to duplications of WRKY transcription factors, however, complicates genetic analysis by allowing single-mutant plants to maintain wild-type phenotypes. Our analyses indicate that three group I WRKY genes, OsWRKY24, -53, and -70, act in a partially redundant manner. All three showed characteristics of typical WRKY transcription factors: each localized to nuclei and yeast one-hybrid assays indicated that they all bind to W-boxes, including those present in their own promoters. Quantitative real time-PCR (qRT-PCR) analyses indicated that the expression levels of the three WRKY genes varied in the different tissues tested. Particle bombardment-mediated transient expression analyses indicated that all three genes repress the GA and ABA signaling in a dosage-dependent manner. Combination of all three WRKY genes showed additive antagonism of ABA and GA signaling. These results suggest that these WRKY proteins function as negative transcriptional regulators of GA and ABA signaling. However, different combinations of these WRKY genes can lead to varied strengths in suppression of their targets.
WRKY转录因子超家族成员对于调控许多植物通路至关重要。然而,由于WRKY转录因子的重复导致功能冗余,使得单突变体植物能够维持野生型表型,从而使遗传分析变得复杂。我们的分析表明,三个I组WRKY基因,即OsWRKY24、-53和-70,以部分冗余的方式发挥作用。这三个基因均表现出典型WRKY转录因子的特征:每个基因都定位于细胞核,酵母单杂交试验表明它们都能与W盒结合,包括存在于其自身启动子中的W盒。定量实时PCR(qRT-PCR)分析表明,这三个WRKY基因的表达水平在不同测试组织中有所不同。粒子轰击介导的瞬时表达分析表明,这三个基因均以剂量依赖的方式抑制GA和ABA信号传导。这三个WRKY基因的组合显示出对ABA和GA信号传导的累加拮抗作用。这些结果表明,这些WRKY蛋白作为GA和ABA信号传导的负转录调节因子发挥作用。然而,这些WRKY基因的不同组合可导致对其靶标的抑制强度不同。