Kim Dae Sung, Kim Nak Hyun, Hwang Byung Kook
Laboratory of Molecular Plant Pathology, College of Life Sciences and Biotechnology, Korea University, Seoul 136-713, Republic of Korea.
Laboratory of Molecular Plant Pathology, College of Life Sciences and Biotechnology, Korea University, Seoul 136-713, Republic of Korea
J Exp Bot. 2015 Apr;66(7):1987-99. doi: 10.1093/jxb/erv001. Epub 2015 Feb 17.
The pepper receptor-like cytoplasmic protein kinase, CaPIK1, which mediates signalling of plant cell death and defence responses was previously identified. Here, the identification of a class IV chitinase, CaChitIV, from pepper plants (Capsicum annuum), which interacts with CaPIK1 and promotes CaPIK1-triggered cell death and defence responses, is reported. CaChitIV contains a signal peptide, chitin-binding domain, and glycol hydrolase domain. CaChitIV expression was up-regulated by Xanthomonas campestris pv. vesicatoria (Xcv) infection. Notably, avirulent Xcv infection rapidly induced CaChitIV expression in pepper leaves. Bimolecular fluorescence complementation and co-immunoprecipitation revealed that CaPIK1 interacts with CaChitIV in planta, and that the CaPIK1-CaChitIV complex is localized mainly in the cytoplasm and plasma membrane. CaChitIV is also localized in the endoplasmic reticulum. Transient co-expression of CaChitIV with CaPIK1 enhanced CaPIK1-triggered cell death response and reactive oxygen species (ROS) and nitric oxide (NO) bursts. Co-silencing of both CaChitIV and CaPIK1 in pepper plants conferred enhanced susceptibility to Xcv infection, which was accompanied by a reduced induction of cell death response, ROS and NO bursts, and defence response genes. Ectopic expression of CaPIK1 in Arabidopsis enhanced basal resistance to Hyaloperonospora arabidopsidis infection. Together, the results suggest that CaChitIV positively regulates CaPIK1-triggered cell death and defence responses through its interaction with CaPIK1.
先前已鉴定出介导植物细胞死亡和防御反应信号传导的辣椒受体样细胞质蛋白激酶CaPIK1。本文报道了从辣椒(Capsicum annuum)中鉴定出一种IV类几丁质酶CaChitIV,它与CaPIK1相互作用,并促进CaPIK1触发的细胞死亡和防御反应。CaChitIV包含一个信号肽、几丁质结合结构域和糖水解酶结构域。CaChitIV的表达受野油菜黄单胞菌疮痂致病变种(Xcv)感染的上调。值得注意的是,无毒的Xcv感染迅速诱导辣椒叶片中CaChitIV的表达。双分子荧光互补和免疫共沉淀显示,CaPIK1在植物体内与CaChitIV相互作用,且CaPIK1-CaChitIV复合物主要定位于细胞质和质膜。CaChitIV也定位于内质网。CaChitIV与CaPIK1的瞬时共表达增强了CaPIK1触发的细胞死亡反应以及活性氧(ROS)和一氧化氮(NO)的爆发。辣椒植株中CaChitIV和CaPIK1的共沉默导致对Xcv感染的易感性增强,同时细胞死亡反应、ROS和NO爆发以及防御反应基因的诱导减少。CaPIK1在拟南芥中的异位表达增强了对阿拉伯假霜霉感染的基础抗性。总之,这些结果表明CaChitIV通过与CaPIK1相互作用正向调节CaPIK1触发的细胞死亡和防御反应。