Clarke J D, Liu Y, Klessig D F, Dong X
Developmental, Cell, and Molecular Biology Group, Department of Botany, Box 91000, Duke University, Durham, North Carolina 27708-1000, USA.
Plant Cell. 1998 Apr;10(4):557-69. doi: 10.1105/tpc.10.4.557.
In Arabidopsis, NPR1 mediates the salicylic acid (SA)-induced expression of pathogenesis-related (PR) genes and systemic acquired resistance (SAR). Here, we report the identification of another component, CPR 6, that may function with NPR1 in regulating PR gene expression. The dominant CPR 6-1 mutant expresses the SA/NPR1-regulated PR genes (PR-1, BGL 2, and PR-5) and displays enhanced resistance to Pseudomonas syringae pv maculicola ES4326 and Peronospora parasitica Noco2 in the absence of SAR induction. cpr 6-1-induced PR gene expression is not suppressed in the cpr 6-1 npr1-1 double mutant but is suppressed when SA is removed by salicylate hydroxylase. Thus, constitutive PR gene expression in cpr 6-1 requires SA but not NPR1. In addition, resistance to P. s. maculicola ES4326 is suppressed in the cpr 6-1 npr1-1 double mutant, despite expression of PR-1, BGL 2, and PR-5. Resistance to P. s. maculicola ES4326 must therefore be accomplished through unidentified antibacterial gene products that are regulated through NPR1. These results show that CPR 6 is an important regulator of multiple signal transduction pathways involved in plant defense.
在拟南芥中,NPR1介导水杨酸(SA)诱导的病程相关(PR)基因的表达以及系统获得性抗性(SAR)。在此,我们报告了另一个组分CPR 6的鉴定,它可能与NPR1共同作用来调节PR基因的表达。显性CPR 6 - 1突变体表达SA/NPR1调节的PR基因(PR - 1、BGL 2和PR - 5),并且在没有SAR诱导的情况下,对丁香假单胞菌番茄致病变种ES4326和寄生霜霉Noco2表现出增强的抗性。在cpr 6 - 1 npr1 - 1双突变体中,cpr 6 - 1诱导的PR基因表达未被抑制,但当水杨酸被水杨酸羟化酶去除时则被抑制。因此,cpr 6 - 1中PR基因的组成型表达需要SA而不是NPR1。此外,尽管PR - 1、BGL 2和PR - 5表达,但在cpr 6 - 1 npr1 - 1双突变体中对丁香假单胞菌番茄致病变种ES4326的抗性被抑制。因此,对丁香假单胞菌番茄致病变种ES4326的抗性必须通过由NPR1调节的未知抗菌基因产物来实现。这些结果表明,CPR 6是植物防御中涉及的多个信号转导途径的重要调节因子。