Qiu Jin-Long, Fiil Berthe Katrine, Petersen Klaus, Nielsen Henrik Bjørn, Botanga Christopher J, Thorgrimsen Stephan, Palma Kristoffer, Suarez-Rodriguez Maria Cristina, Sandbech-Clausen Signe, Lichota Jacek, Brodersen Peter, Grasser Klaus D, Mattsson Ole, Glazebrook Jane, Mundy John, Petersen Morten
Department of Biology, University of Copenhagen, Copenhagen, Denmark.
EMBO J. 2008 Aug 20;27(16):2214-21. doi: 10.1038/emboj.2008.147. Epub 2008 Jul 24.
Plant and animal perception of microbes through pathogen surveillance proteins leads to MAP kinase signalling and the expression of defence genes. However, little is known about how plant MAP kinases regulate specific gene expression. We report that, in the absence of pathogens, Arabidopsis MAP kinase 4 (MPK4) exists in nuclear complexes with the WRKY33 transcription factor. This complex depends on the MPK4 substrate MKS1. Challenge with Pseudomonas syringae or flagellin leads to the activation of MPK4 and phosphorylation of MKS1. Subsequently, complexes with MKS1 and WRKY33 are released from MPK4, and WRKY33 targets the promoter of PHYTOALEXIN DEFICIENT3 (PAD3) encoding an enzyme required for the synthesis of antimicrobial camalexin. Hence, wrky33 mutants are impaired in the accumulation of PAD3 mRNA and camalexin production upon infection. That WRKY33 is an effector of MPK4 is further supported by the suppression of PAD3 expression in mpk4-wrky33 double mutant backgrounds. Our data establish direct links between MPK4 and innate immunity and provide an example of how a plant MAP kinase can regulate gene expression by releasing transcription factors in the nucleus upon activation.
植物和动物通过病原体监测蛋白对微生物的感知会导致丝裂原活化蛋白激酶(MAP激酶)信号传导和防御基因的表达。然而,关于植物MAP激酶如何调节特定基因表达却知之甚少。我们报告称,在没有病原体的情况下,拟南芥MAP激酶4(MPK4)与WRKY33转录因子存在于核复合物中。这种复合物依赖于MPK4底物MKS1。用丁香假单胞菌或鞭毛蛋白进行刺激会导致MPK4的激活以及MKS1的磷酸化。随后,与MKS1和WRKY33形成的复合物从MPK4上释放,并且WRKY33靶向PHYTOALEXIN DEFICIENT3(PAD3)的启动子,PAD3编码一种合成抗微生物植保素camalexin所需的酶。因此,wrky33突变体在感染后PAD3 mRNA的积累和camalexin的产生方面存在缺陷。mpk4 - wrky33双突变背景下PAD3表达的抑制进一步支持了WRKY33是MPK4的效应器这一观点。我们的数据建立了MPK4与先天免疫之间的直接联系,并提供了一个植物MAP激酶如何通过在激活后释放细胞核中的转录因子来调节基因表达的例子。