Urao T, Yakubov B, Satoh R, Yamaguchi-Shinozaki K, Seki M, Hirayama T, Shinozaki K
Biological Resources Division, Japan International Research Center for Agricultural Science (JIRCAS), Ministry of Agriculture, Forestry and Fisheries, 1-2 Oowashi, Tsukuba, Ibaraki 305, Japan.
Plant Cell. 1999 Sep;11(9):1743-54. doi: 10.1105/tpc.11.9.1743.
Water deficit and the resulting osmotic stress affect plant growth. To understand how plant cells monitor and respond to osmotic change from water stress, we isolated a cDNA from dehydrated Arabidopsis plants. This cDNA encodes a novel hybrid-type histidine kinase, ATHK1. Restriction fragment length polymorphism mapping showed that the ATHK1 gene is on chromosome 2. The predicted ATHK1 protein has two putative transmembrane regions in the N-terminal half and has structural similarity to the yeast osmosensor synthetic lethal of N-end rule 1 (SLN1). The ATHK1 transcript was more abundant in roots than other tissues under normal growth conditions and accumulated under conditions of high or low osmolarity. Histochemical analysis of beta-glucuronidase activities driven by the ATHK1 promoter further indicates that the ATHK1 gene is transcriptionally upregulated in response to changes in external osmolarity. Overexpression of the ATHK1 cDNA suppressed the lethality of the temperature-sensitive osmosensing-defective yeast mutant sln1-ts. By contrast, ATHK1 cDNAs in which conserved His or Asp residues had been substituted failed to complement the sln1-ts mutant, indicating that ATHK1 functions as a histidine kinase. Introduction of the ATHK1 cDNA into the yeast double mutant sln1Delta sho1Delta, which lacks two osmosensors, suppressed lethality in high-salinity media and activated the high-osmolarity glycerol response 1 (HOG1) mitogen-activated protein kinase (MAPK). These results imply that ATHK1 functions as an osmosensor and transmits the stress signal to a downstream MAPK cascade.
水分亏缺及由此产生的渗透胁迫会影响植物生长。为了解植物细胞如何监测并响应水分胁迫引起的渗透变化,我们从脱水的拟南芥植株中分离出一个cDNA。该cDNA编码一种新型杂合型组氨酸激酶,即ATHK1。限制性片段长度多态性图谱分析表明ATHK1基因位于第2号染色体上。预测的ATHK1蛋白在N端的一半区域有两个假定的跨膜区,并且在结构上与酵母渗透感受器N端规则1合成致死蛋白(SLN1)相似。在正常生长条件下,ATHK1转录本在根中的丰度高于其他组织,并且在高渗或低渗条件下会积累。对由ATHK1启动子驱动的β-葡萄糖醛酸酶活性进行的组织化学分析进一步表明,ATHK1基因会响应外部渗透压的变化而在转录水平上上调。ATHK1 cDNA的过表达抑制了温度敏感型渗透感应缺陷酵母突变体sln1-ts的致死性。相比之下,保守的组氨酸或天冬氨酸残基被取代的ATHK1 cDNA无法互补sln1-ts突变体,这表明ATHK1作为组氨酸激酶发挥作用。将ATHK1 cDNA导入缺乏两种渗透感受器的酵母双突变体sln1Δsho1Δ中,可抑制高盐培养基中的致死性并激活高渗甘油反应1(HOG1)丝裂原活化蛋白激酶(MAPK)。这些结果表明ATHK1作为一种渗透感受器发挥作用,并将胁迫信号传递至下游的MAPK级联反应。