Foley Rhonda C, Sappl Pia G, Perl-Treves Rafael, Millar A Harvey, Singh Karam B
Commonwealth Scientific and Industrial Research Organization Plant Industry, Centre for Environmental and Life Sciences, Wembley, Western Australia 6913, Australia.
Plant Physiol. 2006 Sep;142(1):245-53. doi: 10.1104/pp.106.079509. Epub 2006 Jul 7.
The Arabidopsis (Arabidopsis thaliana) GSTF8 gene is a member of the glutathione S-transferase (GST) family whose expression is induced by defense signals, certain chemical stresses, and some pathogens. Here, we have used transgenic plants and an in vivo imaging system to demonstrate that GSTF8 expression is subject to a distinct desensitization phenomenon because prior chemical treatment significantly reduces reactivation of the GSTF8 promoter by hydrogen peroxide, auxin, and salicylic acid. A GSTF8 null line had similar desensitization properties to wild type, demonstrating that GSTF8 protein levels are not responsible for desensitization. The resulting refractory period is unusually long lasting, with full recovery taking 4 d. Expression of the GSTF8 promoter following a second treatment occurred predominantly in newly formed tissue at the root tip, suggesting that desensitization is lost upon cell division. Expression of the endogenous GSTF8 gene and another GST gene, GSTF6, is also desensitized following treatment with hydrogen peroxide. The desensitization phenomenon can be activated by a very low concentration of inducer that is not sufficient to activate the GSTF8 promoter. These results demonstrate that activation of the GSTF8 promoter is not essential for eliciting desensitization. A key promoter sequence within the GSTF8 gene, the ocs element, is also affected by desensitization. Treatment with a phosphatase inhibitor prevents desensitization of GSTF8 expression and ocs element activity, suggesting that dephosphorylation of one or more proteins is required for desensitization to occur.
拟南芥(Arabidopsis thaliana)的GSTF8基因是谷胱甘肽S-转移酶(GST)家族的成员,其表达受防御信号、某些化学胁迫和一些病原体的诱导。在这里,我们使用转基因植物和体内成像系统来证明GSTF8的表达存在一种独特的脱敏现象,因为先前的化学处理显著降低了过氧化氢、生长素和水杨酸对GSTF8启动子的再激活作用。一个GSTF8缺失系具有与野生型相似的脱敏特性,这表明GSTF8蛋白水平与脱敏无关。由此产生的不应期异常持久,完全恢复需要4天。第二次处理后GSTF8启动子的表达主要发生在根尖新形成的组织中,这表明脱敏在细胞分裂时消失。用过氧化氢处理后,内源性GSTF8基因和另一个GST基因GSTF6的表达也会脱敏。极低浓度的诱导剂就能激活脱敏现象,而该浓度不足以激活GSTF8启动子。这些结果表明,GSTF8启动子的激活对于引发脱敏并非必不可少。GSTF8基因内的一个关键启动子序列ocs元件也受到脱敏的影响。用磷酸酶抑制剂处理可防止GSTF8表达和ocs元件活性的脱敏,这表明脱敏发生需要一种或多种蛋白质的去磷酸化。