Lee Hyo-Jun, Park Young-Joon, Seo Pil Joon, Kim Ju-Heon, Sim Hee-Jung, Kim Sang-Gyu, Park Chung-Mo
Department of Chemistry, Seoul National University, Seoul 151-742, Korea.
Department of Chemistry, Chonbuk National University, Jeonju 561-756, Korea.
Plant Cell. 2015 Dec;27(12):3425-38. doi: 10.1105/tpc.15.00371. Epub 2015 Dec 15.
In plants, necrotic lesions occur at the site of pathogen infection through the hypersensitive response, which is followed by induction of systemic acquired resistance (SAR) in distal tissues. Salicylic acid (SA) induces SAR by activating NONEXPRESSER OF PATHOGENESIS-RELATED GENES1 (NPR1) through an oligomer-to-monomer reaction. However, SA biosynthesis is elevated only slightly in distal tissues during SAR, implying that SA-mediated induction of SAR requires additional factors. Here, we demonstrated that SA-independent systemic signals induce a gene encoding SNF1-RELATED PROTEIN KINASE 2.8 (SnRK2.8), which phosphorylates NPR1 during SAR. The SnRK2.8-mediated phosphorylation of NPR1 is necessary for its nuclear import. Notably, although SnRK2.8 transcription and SnRK2.8 activation are independent of SA signaling, the SnRK2.8-mediated induction of SAR requires SA. Together with the SA-mediated monomerization of NPR1, these observations indicate that SA signals and SnRK2.8-mediated phosphorylation coordinately function to activate NPR1 via a dual-step process in developing systemic immunity in Arabidopsis thaliana.
在植物中,坏死性病变通过超敏反应在病原体感染部位发生,随后在远端组织中诱导系统性获得性抗性(SAR)。水杨酸(SA)通过寡聚体到单体的反应激活病程相关基因非表达子1(NPR1)来诱导SAR。然而,在SAR过程中,远端组织中的SA生物合成仅略有升高,这意味着SA介导的SAR诱导需要其他因素。在这里,我们证明了不依赖SA的系统性信号诱导一个编码SNF1相关蛋白激酶2.8(SnRK2.8)的基因,该基因在SAR过程中使NPR1磷酸化。SnRK2.8介导的NPR1磷酸化是其核输入所必需的。值得注意的是,尽管SnRK2.8的转录和激活独立于SA信号传导,但SnRK2.8介导的SAR诱导需要SA。这些观察结果与SA介导的NPR1单体化一起表明,SA信号和SnRK2.8介导的磷酸化在拟南芥系统性免疫发育过程中通过两步过程协同作用以激活NPR1。