Clarke J D, Volko S M, Ledford H, Ausubel F M, Dong X
Developmental, Cell, and Molecular Biology Group, Department of Biology, Duke University, Durham, North Carolina 27708-1000, USA.
Plant Cell. 2000 Nov;12(11):2175-90. doi: 10.1105/tpc.12.11.2175.
Disease resistance in Arabidopsis is regulated by multiple signal transduction pathways in which salicylic acid (SA), jasmonic acid (JA), and ethylene (ET) function as key signaling molecules. Epistasis analyses were performed between mutants that disrupt these pathways (npr1, eds5, ein2, and jar1) and mutants that constitutively activate these pathways (cpr1, cpr5, and cpr6), allowing exploration of the relationship between the SA- and JA/ET-mediated resistance responses. Two important findings were made. First, the constitutive disease resistance exhibited by cpr1, cpr5, and cpr6 is completely suppressed by the SA-deficient eds5 mutant but is only partially affected by the SA-insensitive npr1 mutant. Moreover, eds5 suppresses the SA-accumulating phenotype of the cpr mutants, whereas npr1 enhances it. These data indicate the existence of an SA-mediated, NPR1-independent resistance response. Second, the ET-insensitive mutation ein2 and the JA-insensitive mutation jar1 suppress the NPR1-independent resistance response exhibited by cpr5 and cpr6. Furthermore, ein2 potentiates SA accumulation in cpr5 and cpr5 npr1 while dampening SA accumulation in cpr6 and cpr6 npr1. These latter results indicate that cpr5 and cpr6 regulate resistance through distinct pathways and that SA-mediated, NPR1-independent resistance works in combination with components of the JA/ET-mediated response pathways.
拟南芥中的抗病性由多种信号转导途径调控,其中水杨酸(SA)、茉莉酸(JA)和乙烯(ET)作为关键信号分子发挥作用。对破坏这些途径的突变体(npr1、eds5、ein2和jar1)与组成型激活这些途径的突变体(cpr1、cpr5和cpr6)进行了上位性分析,从而探究SA介导的抗性反应与JA/ET介导的抗性反应之间的关系。得出了两个重要发现。首先,cpr1、cpr5和cpr6所表现出的组成型抗病性被SA缺陷型eds5突变体完全抑制,但仅受到SA不敏感型npr1突变体的部分影响。此外,eds5抑制了cpr突变体的SA积累表型,而npr1则增强了该表型。这些数据表明存在一种SA介导的、不依赖NPR1的抗性反应。其次,ET不敏感突变体ein2和JA不敏感突变体jar1抑制了cpr5和cpr6所表现出的不依赖NPR1的抗性反应。此外,ein2增强了cpr5和cpr5 npr1中的SA积累,同时减弱了cpr6和cpr6 npr1中的SA积累。后一组结果表明,cpr5和cpr6通过不同途径调节抗性,并且SA介导的、不依赖NPR1的抗性与JA/ET介导的反应途径的组分协同作用。