Pitzschke Andrea, Djamei Armin, Teige Markus, Hirt Heribert
Department of Plant Molecular Biology, Max F Perutz Laboratories, University of Vienna, 1030 Vienna, Austria.
Proc Natl Acad Sci U S A. 2009 Oct 27;106(43):18414-9. doi: 10.1073/pnas.0905599106. Epub 2009 Oct 9.
The plant pathogen Agrobacterium tumefaciens transforms plant cells by delivering its T-DNA into the plant cell nucleus where it integrates into the plant genome and causes tumor formation. A key role of VirE2-interacting protein 1 (VIP1) in the nuclear import of T-DNA during Agrobacterium-mediated plant transformation has been unravelled and VIP1 was shown to undergo nuclear localization upon phosphorylation by the mitogen-activated protein kinase MPK3. Here, we provide evidence that VIP1 encodes a functional bZIP transcription factor that stimulates stress-dependent gene expression by binding to VIP1 response elements (VREs), a DNA hexamer motif. VREs are overrepresented in promoters responding to activation of the MPK3 pathway such as Trxh8 and MYB44. Accordingly, plants overexpressing VIP1 accumulate high levels of Trxh8 and MYB44 transcripts, whereas stress-induced expression of these genes is impaired in mpk3 mutants. Trxh8 and MYB44 promoters are activated by VIP1 in a VRE-dependent manner. VIP1 strongly enhances expression from a synthetic promoter harboring multiple VRE copies and directly interacts with VREs in vitro and in vivo. Chromatin immunoprecipitation assays of the MYB44 promoter confirm that VIP1 binding to VREs is enhanced under conditions of MPK3 pathway stimulation. These results provide molecular insight into the cellular mechanism of target gene regulation by the MPK3 pathway.
植物病原菌根癌农杆菌通过将其T-DNA导入植物细胞核来转化植物细胞,T-DNA会整合到植物基因组中并导致肿瘤形成。已揭示了VirE2相互作用蛋白1(VIP1)在农杆菌介导的植物转化过程中T-DNA核输入中的关键作用,并且显示VIP1在被丝裂原活化蛋白激酶MPK3磷酸化后会发生核定位。在此,我们提供证据表明VIP1编码一种功能性bZIP转录因子,该因子通过与VIP1反应元件(VREs,一种DNA六聚体基序)结合来刺激应激依赖性基因表达。VREs在响应MPK3途径激活的启动子(如Trxh8和MYB44)中过度富集。因此,过表达VIP1的植物积累高水平的Trxh8和MYB44转录本,而这些基因在mpk3突变体中的应激诱导表达受损。Trxh8和MYB44启动子以VRE依赖性方式被VIP1激活。VIP1强烈增强含有多个VRE拷贝的合成启动子的表达,并在体外和体内直接与VREs相互作用。对MYB44启动子的染色质免疫沉淀分析证实,在MPK3途径刺激的条件下,VIP1与VREs的结合增强。这些结果为MPK3途径调控靶基因的细胞机制提供了分子见解。