State Key Laboratory of Agrobiotechnology and National Center for Plant Gene Research (Beijing), China Agricultural University, Beijing 100193, China.
Plant J. 2009 Dec;60(5):757-70. doi: 10.1111/j.1365-313X.2009.03995.x. Epub 2009 Aug 13.
Arabidopsis gain-of-resistance mutants, which show HR-like lesion formation and SAR-like constitutive defense responses, were used well as tools to unravel the plant defense mechanisms. We have identified a novel mutant, designated constitutive expresser of PR genes 30 (cpr30), that exhibited dwarf morphology, constitutive resistance to the bacterial pathogen Pseudomonas syringae and the dramatic induction of defense-response gene expression. The cpr30-conferred growth defect morphology and defense responses are dependent on ENHANCED DISEASE SUSCEPTIBILITY 1 (EDS1), PHYTOALEXIN DEFICIENT 4 (PAD4), and NONRACE-SPECIFIC DISEASE RESISTANCE 1 (NDR1). Further studies demonstrated that salicylic acid (SA) could partially account for the cpr30-conferred constitutive PR1 gene expression, but not for the growth defect, and that the cpr30-conferred defense responses were NPR1 independent. We observed a widespread expression of CPR30 throughout the plant, and a localization of CPR30-GFP fusion protein in the cytoplasm and nucleus. As an F-box protein, CPR30 could interact with multiple Arabidopsis-SKP1-like (ASK) proteins in vivo. Co-localization of CPR30 and ASK1 or ASK2 was observed in Arabidopsis protoplasts. Based on these results, we conclude that CPR30, a novel negative regulator, regulates both SA-dependent and SA-independent defense signaling, most likely through the ubiquitin-proteasome pathway in Arabidopsis.
拟南芥抗病突变体,表现出类似过敏性坏死反应(HR)的病斑形成和系统获得性抗性(SAR)的组成型防御反应,被广泛用作揭示植物防御机制的工具。我们鉴定了一个新的突变体,命名为组成型 PR 基因表达 30 号(cpr30),其表现为矮化表型、对细菌病原体丁香假单胞菌具有组成型抗性,以及防御反应基因表达的显著诱导。cpr30 赋予的生长缺陷表型和防御反应依赖于增强型疾病易感性 1(EDS1)、植物抗毒素缺失 4(PAD4)和非专化性疾病抗性 1(NDR1)。进一步的研究表明,水杨酸(SA)可以部分解释 cpr30 赋予的组成型 PR1 基因表达,但不能解释生长缺陷,并且 cpr30 赋予的防御反应不依赖于 NPR1。我们观察到 CPR30 在整个植物中广泛表达,并观察到 CPR30-GFP 融合蛋白在细胞质和细胞核中的定位。作为一种 F-box 蛋白,CPR30 可以在体内与多个拟南芥-SKP1 样(ASK)蛋白相互作用。在拟南芥原生质体中观察到 CPR30 与 ASK1 或 ASK2 的共定位。基于这些结果,我们得出结论,CPR30 作为一个新的负调控因子,调节依赖于 SA 和不依赖于 SA 的防御信号转导,可能是通过拟南芥中的泛素-蛋白酶体途径。