Shandong Provincial Key Laboratory of Plant Stress, College of Life Sciences, Shandong Normal University, Jinan, 250014, China.
Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Plant Mol Biol. 2020 Apr;102(6):603-614. doi: 10.1007/s11103-020-00966-4. Epub 2020 Feb 12.
The WRKY transcription factor family is involved in responding to biotic and abiotic stresses. Its members contain a typical WRKY domain and can regulate plant physiological responses by binding to W-boxes in the promoter regions of downstream target genes. We identified the sweet sorghum SbWRKY50 (Sb09g005700) gene, which encodes a typical class II of the WRKY family protein that localizes to the nucleus and has transcriptional activation activity. The expression of SbWRKY50 in sweet sorghum was reduced by salt stress, and its ectopic expression reduced the salt tolerance of Arabidopsis thaliana plants. Compared with the wild type, the germination rate, root length, biomass and potassium ion content of SbWRKY50 over-expression plants decreased significantly under salt-stress conditions, while the hydrogen peroxide, superoxide anion and sodium ion contents increased. Real-time PCR results showed that the expression levels of AtSOS1, AtHKT1 and genes related to osmotic and oxidative stresses in over-expression strains decreased under salt-stress conditions. Luciferase complementation imaging and yeast one-hybrid assays confirmed that SbWRKY50 could directly bind to the upstream promoter of the SOS1 gene in A. thaliana. However, in sweet sorghum, SbWRKY50 could directly bind to the upstream promoters of SOS1 and HKT1. These results suggest that the new WRKY transcription factor SbWRKY50 participates in plant salt response by controlling ion homeostasis. However, the regulatory mechanisms are different in sweet sorghum and Arabidopsis, which may explain their different salt tolerance levels. The data provide information that can be applied to genetically modifying salt tolerance in different crop varieties.
WRKY 转录因子家族参与生物和非生物胁迫的响应。其成员包含一个典型的 WRKY 结构域,并可以通过结合下游靶基因启动子区域中的 W-框来调节植物的生理反应。我们鉴定了甜高粱 SbWRKY50(Sb09g005700)基因,该基因编码一个典型的 II 类 WRKY 家族蛋白,定位于细胞核中,具有转录激活活性。盐胁迫下甜高粱 SbWRKY50 的表达减少,其异位表达降低了拟南芥植物的耐盐性。与野生型相比,SbWRKY50 过表达植株在盐胁迫条件下的发芽率、根长、生物量和钾离子含量显著降低,而过氧化物酶、超氧阴离子和钠离子含量增加。实时 PCR 结果表明,盐胁迫条件下过表达株系中与 SOS1、AtHKT1 和渗透及氧化胁迫相关的基因表达水平降低。荧光素酶互补成像和酵母单杂交试验证实 SbWRKY50 可直接结合拟南芥 SOS1 基因的上游启动子。然而,在甜高粱中,SbWRKY50 可以直接结合 SOS1 和 HKT1 的上游启动子。这些结果表明,新的 WRKY 转录因子 SbWRKY50 通过控制离子稳态参与植物的盐响应。然而,在甜高粱和拟南芥中的调控机制不同,这可能解释了它们不同的耐盐水平。这些数据为不同作物品种遗传改良耐盐性提供了信息。