Department of Plant Biotechnology , Chonnam National University, Buk-Gu, Gwangju 500-757, Korea.
Plant Physiol. 2013 Jan;161(1):408-24. doi: 10.1104/pp.112.207621. Epub 2012 Nov 2.
The Arabidopsis (Arabidopsis thaliana) two-component signaling system, which is composed of sensor histidine kinases, histidine phosphotransfer proteins, and response regulators, mediates the cytokinin response and various other plant responses. We have previously shown that ARABIDOPSIS HISTIDINE KINASE2 (AHK2), AHK3, and cold-inducible type A ARABIDOPSIS RESPONSE REGULATORS (ARRs) play roles in cold signaling. However, the roles of type B ARRs and ARABIDOPSIS HISTIDINE PHOSPHOTRANSFER PROTEINS (AHPs) have not been investigated in cold signaling. Here, we show that ARR1 and AHP2, AHP3, and AHP5 play positive roles in the cold-inducible expression of type A ARRs. arr1 mutants showed greatly reduced cold-responsive expression of type A ARRs compared with the wild type, whereas ARR1-overexpressing Arabidopsis exhibited the hypersensitive cold response of type A ARRs as well as enhanced freezing tolerance with cytokinin, suggesting that ARR1 functions as a positive factor of cold signaling. Transgenic Arabidopsis expressing ARR1ΔDDK:GR lacking the amino-terminal receiver domain showed wild-type expression levels of type A ARRs in response to cold, indicating that the signal receiver domain of ARR1 might be important for cold-responsive expression of type A ARRs. ahp2 ahp3 ahp5 triple mutations greatly reduced type A ARR expression in response to cold, whereas the single or double ahp mutants displayed wild-type levels of ARR expression, suggesting that AHP2, AHP3, and AHP5 are redundantly involved in cold signaling. Taken together, these results suggest that ARR1 mediates cold signal via AHP2, AHP3, or AHP5 from AHK2 and AHK3 to express type A ARRs. We further identified a cold transcriptome affected by ahk2 ahk3 mutations by microarray analysis, revealing a new cold-responsive gene network regulated downstream of AHK2 and AHK3.
拟南芥(Arabidopsis thaliana)的双组分信号系统由感应组氨酸激酶、组氨酸磷酸转移蛋白和应答调节因子组成,介导细胞分裂素反应和各种其他植物反应。我们之前已经表明,ARABIDOPSIS HISTIDINE KINASE2(AHK2)、AHK3 和冷诱导型 A 拟南芥应答调节因子(ARRs)在冷信号转导中发挥作用。然而,B 型 ARRs 和 ARABIDOPSIS HISTIDINE PHOSPHOTRANSFER PROTEINS(AHPs)在冷信号转导中的作用尚未得到研究。在这里,我们表明 ARR1 和 AHP2、AHP3 和 AHP5 在 A 型 ARRs 的冷诱导表达中发挥积极作用。与野生型相比,arr1 突变体中 A 型 ARRs 的冷诱导表达大大降低,而过表达 ARR1 的拟南芥表现出 A 型 ARRs 的超敏冷反应以及细胞分裂素增强的耐冻性,表明 ARR1 作为冷信号的正因子发挥作用。表达 ARR1ΔDDK:GR(缺少氨基末端受体结构域)的转基因拟南芥对冷的反应表现出 A 型 ARRs 的野生型表达水平,表明 ARR1 的信号受体结构域可能对 A 型 ARRs 的冷诱导表达很重要。ahp2 ahp3 ahp5 三重突变体大大降低了 A 型 ARRs 对冷的反应表达,而单个或双 ahp 突变体则表现出 A 型 ARR 表达的野生型水平,表明 AHP2、AHP3 和 AHP5 冗余地参与冷信号转导。综上所述,这些结果表明 ARR1 通过 AHP2、AHP3 或 AHP5 介导 AHK2 和 AHK3 到 A 型 ARRs 的冷信号转导。我们进一步通过微阵列分析鉴定了一个受 ahk2 ahk3 突变影响的冷转录组,揭示了一个由 AHK2 和 AHK3 下游调控的新的冷反应基因网络。