Böhnert Heidi U, Fudal Isabelle, Dioh Waly, Tharreau Didier, Notteghem Jean-Loup, Lebrun Marc-Henri
FRE 2579 Centre National de la Recherche Scientifique/Bayer CropScience, F-69263 Lyon Cedex 09, France.
Plant Cell. 2004 Sep;16(9):2499-513. doi: 10.1105/tpc.104.022715. Epub 2004 Aug 19.
Isolates of the rice blast fungus Magnaporthe grisea that carry the gene encoding Avirulence Conferring Enzyme1 (ACE1) are specifically recognized by rice (Oryza sativa) cultivars carrying the resistance gene Pi33. This recognition enables resistant plants to activate a defense response. ACE1 was isolated by map-based cloning and encodes a putative hybrid between a polyketide synthase and a nonribosomal peptide synthetase, enzymes involved in microbial secondary metabolism. ACE1 is expressed exclusively during fungal penetration of host leaves, the time point at which plant defense reactions are triggered. Ace1 appears to be localized in the cytoplasm of the appressorium. Mutation of the putative catalytic site of the beta-ketoacyl synthase domain of Ace1 abolishes recognition of the fungus by resistant rice. This suggests that Ace1 biosynthetic activity is required for avirulence. Our results are consistent with the hypothesis that the fungal signal recognized by resistant rice plants is the secondary metabolite whose synthesis depends on Ace1.
携带编码无毒力赋予酶1(ACE1)基因的稻瘟病菌(Magnaporthe grisea)分离株,会被携带抗性基因Pi33的水稻(Oryza sativa)品种特异性识别。这种识别使抗性植物能够激活防御反应。ACE1通过图位克隆分离得到,编码一种假定的聚酮合酶和非核糖体肽合成酶的杂交体,这两种酶参与微生物次级代谢。ACE1仅在真菌穿透宿主叶片期间表达,这是触发植物防御反应的时间点。Ace1似乎定位于附着胞的细胞质中。Ace1的β-酮酰基合成酶结构域假定催化位点的突变消除了抗性水稻对真菌的识别。这表明Ace1的生物合成活性是无毒力所必需的。我们的结果与以下假设一致,即抗性水稻植株识别的真菌信号是其合成依赖于Ace1的次级代谢产物。