Suarez-Rodriguez Maria Cristina, Adams-Phillips Lori, Liu Yidong, Wang Huachun, Su Shih-Heng, Jester Peter J, Zhang Shuqun, Bent Andrew F, Krysan Patrick J
Department of Horticulture and Genome Center of Wisconsin, University of Wisconsin, Madison, Wisconsin 53706, USA.
Plant Physiol. 2007 Feb;143(2):661-9. doi: 10.1104/pp.106.091389. Epub 2006 Dec 1.
The Arabidopsis (Arabidopsis thaliana) gene MEKK1 encodes a mitogen-activated protein kinase kinase kinase that has been implicated in the activation of the map kinases MPK3 and MPK6 in response to the flagellin elicitor peptide flg22. In this study, analysis of plants carrying T-DNA knockout alleles indicated that MEKK1 is required for flg22-induced activation of MPK4 but not MPK3 or MPK6. Experiments performed using a kinase-impaired version of MEKK1 (K361M) showed that the kinase activity of MEKK1 may not be required for flg22-induced MPK4 activation or for other macroscopic FLS2-mediated responses. MEKK1 may play a structural role in signaling, independent of its protein kinase activity. mekk1 knockout mutants display a severe dwarf phenotype, constitutive callose deposition, and constitutive expression of pathogen response genes. This dwarf phenotype was largely rescued by introduction into mekk1 knockout plants of either the MEKK1 (K361M) construct or a nahG transgene that degrades salicylic acid. When treated with pathogenic bacteria, the K361M plants were slightly more susceptible to an avirulent strain of Pseudomonas syringae and showed a delayed hypersensitive response, suggesting a role for MEKK1 kinase activity in this aspect of plant disease resistance. Our results indicate that MEKK1 acts upstream of MPK4 as a negative regulator of pathogen response pathways, a function that may not require MEKK1's full kinase activity.
拟南芥(Arabidopsis thaliana)基因MEKK1编码一种丝裂原活化蛋白激酶激酶激酶,该激酶参与响应鞭毛蛋白激发肽flg22激活促分裂原活化蛋白激酶MPK3和MPK6。在本研究中,对携带T-DNA敲除等位基因的植株分析表明,MEKK1是flg22诱导的MPK4激活所必需的,但不是MPK3或MPK6激活所必需的。使用MEKK1的激酶受损版本(K361M)进行的实验表明,flg22诱导的MPK4激活或其他宏观的FLS2介导的反应可能不需要MEKK1的激酶活性。MEKK1可能在信号传导中发挥结构作用,与其蛋白激酶活性无关。mekk1敲除突变体表现出严重的矮化表型、组成型胼胝质沉积和病原体反应基因的组成型表达。通过将MEKK1(K361M)构建体或降解水杨酸的nahG转基因导入mekk1敲除植株,这种矮化表型在很大程度上得到了挽救。用病原菌处理时,K361M植株对丁香假单胞菌无毒菌株的敏感性略高,且过敏反应延迟,这表明MEKK1激酶活性在植物抗病性的这一方面发挥作用。我们的结果表明,MEKK1作为病原体反应途径的负调节因子在MPK4上游起作用,这一功能可能不需要MEKK1的全部激酶活性。