Umezawa Taishi, Yoshida Riichiro, Maruyama Kyonoshin, Yamaguchi-Shinozaki Kazuko, Shinozaki Kazuo
Laboratory of Plant Molecular Biology, RIKEN Tsukuba Institute, 3-1-1 Kouyadai, Tsukuba 305-0074, Japan.
Proc Natl Acad Sci U S A. 2004 Dec 7;101(49):17306-11. doi: 10.1073/pnas.0407758101. Epub 2004 Nov 23.
Protein phosphorylation/dephosphorylation are major signaling events induced by osmotic stress in higher plants. Here, we showed that a SNF1-related protein kinase 2 (SnRK2), SRK2C, is an osmotic-stress-activated protein kinase in Arabidopsis thaliana that can significantly impact drought tolerance of Arabidopsis plants. Knockout mutants of SRK2C exhibited drought hypersensitivity in their roots, suggesting that SRK2C is a positive regulator of drought tolerance in Arabidopsis roots. Additionally, transgenic plants with CaMV35S promoter::SRK2C-GFP displayed higher overall drought tolerance than control plants. Whereas stomatal regulation in 35S::SRK2C-GFP plants was not altered, microarray analysis revealed that their drought tolerance coincided with up-regulation of many stress-responsive genes, for example, RD29A, COR15A, and DREB1A/CBF3. From these results, we concluded that SRK2C is capable of mediating signals initiated during drought stress, resulting in appropriate gene expression. Our present study reveals new insights around signal output from osmotic-stress-activated SnRK2 protein kinase as well as supporting feasibility of manipulating SnRK2 toward improving plant osmotic-stress tolerance.
蛋白质磷酸化/去磷酸化是高等植物中由渗透胁迫诱导的主要信号事件。在此,我们表明一种与SNF1相关的蛋白激酶2(SnRK2),即SRK2C,是拟南芥中一种渗透胁迫激活的蛋白激酶,它能显著影响拟南芥植株的耐旱性。SRK2C的敲除突变体在根部表现出干旱超敏性,这表明SRK2C是拟南芥根部耐旱性的正调控因子。此外,带有CaMV35S启动子::SRK2C - GFP的转基因植株比对照植株表现出更高的整体耐旱性。虽然35S::SRK2C - GFP植株的气孔调节没有改变,但微阵列分析显示它们的耐旱性与许多胁迫响应基因的上调相一致,例如RD29A、COR15A和DREB1A/CBF3。基于这些结果,我们得出结论,SRK2C能够介导干旱胁迫期间启动的信号,从而导致适当的基因表达。我们目前的研究揭示了关于渗透胁迫激活的SnRK2蛋白激酶信号输出的新见解,同时也支持了通过操纵SnRK2来提高植物渗透胁迫耐受性的可行性。