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拟南芥促分裂原活化蛋白激酶激酶MKK3位于C组促分裂原活化蛋白激酶上游,并参与病原体信号传导。

The Arabidopsis mitogen-activated protein kinase kinase MKK3 is upstream of group C mitogen-activated protein kinases and participates in pathogen signaling.

作者信息

Dóczi Róbert, Brader Günter, Pettkó-Szandtner Aladár, Rajh Iva, Djamei Armin, Pitzschke Andrea, Teige Markus, Hirt Heribert

机构信息

Department of Plant Molecular Biology, Max F. Perutz Laboratories, University of Viena, A-1030 Viena, Austria.

出版信息

Plant Cell. 2007 Oct;19(10):3266-79. doi: 10.1105/tpc.106.050039. Epub 2007 Oct 12.

Abstract

Although the Arabidopsis thaliana genome contains genes encoding 20 mitogen-activated protein kinases (MAPKs) and 10 MAPK kinases (MAPKKs), most of them are still functionally uncharacterized. In this work, we analyzed the function of the group B MAPK kinase, MKK3. Transgenic ProMKK3:GUS lines showed basal expression in vascular tissues that was strongly induced by Pseudomonas syringae pv tomato strain DC3000 (Pst DC3000) infection but not by abiotic stresses. The growth of virulent Pst DC3000 was increased in mkk3 knockout plants and decreased in MKK3-overexpressing plants. Moreover, MKK3 overexpression lines showed increased expression of several PR genes. By yeast two-hybrid analysis, coimmunoprecipitation, and protein kinase assays, MKK3 was revealed to be an upstream activator of the group C MAPKs MPK1, MPK2, MPK7, and MPK14. Flagellin-derived flg22 peptide strongly activated MPK6 but resulted in poor activation of MPK7. By contrast, MPK6 and MPK7 were both activated by H(2)O(2), but only MPK7 activation was enhanced by MKK3. In agreement with the notion that MKK3 regulates the expression of PR genes, ProPR1:GUS expression was strongly enhanced by coexpression of MKK3-MPK7. Our results reveal that the MKK3 pathway plays a role in pathogen defense and further underscore the importance and complexity of MAPK signaling in plant stress responses.

摘要

尽管拟南芥基因组包含编码20种丝裂原活化蛋白激酶(MAPK)和10种MAPK激酶(MAPKK)的基因,但其中大多数的功能仍未得到表征。在这项研究中,我们分析了B组MAPK激酶MKK3的功能。转基因ProMKK3:GUS株系在维管组织中呈现基础表达,这种表达在丁香假单胞菌番茄致病变种DC3000(Pst DC3000)感染后被强烈诱导,但在非生物胁迫下未被诱导。在mkk3基因敲除植物中,毒性Pst DC3000的生长增加,而在MKK3过表达植物中则减少。此外,MKK3过表达株系中几个病程相关(PR)基因的表达增加。通过酵母双杂交分析、免疫共沉淀和蛋白激酶分析,发现MKK3是C组MAPK MPK1、MPK2、MPK7和MPK14的上游激活剂。鞭毛蛋白衍生的flg22肽强烈激活MPK6,但对MPK7的激活效果较差。相比之下,MPK6和MPK7都能被H₂O₂激活,但只有MPK7的激活能被MKK3增强。与MKK3调节PR基因表达的观点一致,ProPR1:GUS的表达通过共表达MKK3 - MPK7而强烈增强。我们的结果表明,MKK3途径在病原体防御中发挥作用,并进一步强调了MAPK信号传导在植物应激反应中的重要性和复杂性。

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