Wang Rong, Jing Wen, Xiao Longyun, Jin Yakang, Shen Like, Zhang Wenhua
State Key Laboratory of Crop Genetics and Germplasm Enhancement, College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, People's Republic of China.
State Key Laboratory of Crop Genetics and Germplasm Enhancement, College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, People's Republic of China
Plant Physiol. 2015 Jul;168(3):1076-90. doi: 10.1104/pp.15.00298. Epub 2015 May 19.
Sodium transporters play key roles in plant tolerance to salt stress. Here, we report that a member of the High-Affinity K(+) Transporter (HKT) family, OsHKT1;1, in rice (Oryza sativa 'Nipponbare') plays an important role in reducing Na(+) accumulation in shoots to cope with salt stress. The oshkt1;1 mutant plants displayed hypersensitivity to salt stress. They contained less Na(+) in the phloem sap and accumulated more Na(+) in the shoots compared with the wild type. OsHKT1;1 was expressed mainly in the phloem of leaf blades and up-regulated in response to salt stress. Using a yeast one-hybrid approach, a novel MYB coiled-coil type transcription factor, OsMYBc, was found to bind to the OsHKT1;1 promoter. In vivo chromatin immunoprecipitation and in vitro electrophoresis mobility shift assays demonstrated that OsMYBc binds to AAANATNC(C/T) fragments within the OsHKT1;1 promoter. Mutation of the OsMYBc-binding nucleotides resulted in a decrease in promoter activity of OsHKT1;1. Knockout of OsMYBc resulted in a reduction in NaCl-induced expression of OsHKT1;1 and salt sensitivity. Taken together, these results suggest that OsHKT1;1 has a role in controlling Na(+) concentration and preventing sodium toxicity in leaf blades and is regulated by the OsMYBc transcription factor.
钠转运蛋白在植物耐盐胁迫中发挥关键作用。在此,我们报道水稻(Oryza sativa 'Nipponbare')中高亲和性钾转运蛋白(HKT)家族的一个成员OsHKT1;1在减少地上部钠积累以应对盐胁迫方面发挥重要作用。oshkt1;1突变体植株对盐胁迫表现出超敏反应。与野生型相比,它们韧皮部汁液中的钠含量更低,而地上部积累的钠更多。OsHKT1;1主要在叶片韧皮部表达,并在盐胁迫下上调。通过酵母单杂交方法,发现一个新的MYB卷曲螺旋型转录因子OsMYBc可与OsHKT1;1启动子结合。体内染色质免疫沉淀和体外电泳迁移率变动分析表明,OsMYBc与OsHKT1;1启动子内的AAANATNC(C/T)片段结合。OsMYBc结合核苷酸的突变导致OsHKT1;1启动子活性降低。敲除OsMYBc导致NaCl诱导的OsHKT1;1表达降低和盐敏感性增加。综上所述,这些结果表明OsHKT1;1在控制叶片中钠浓度和防止钠毒害方面发挥作用,并受OsMYBc转录因子调控。