Balhadère P V, Talbot N J
School of Biological Sciences, University of Exeter, Washington Singer Laboratories, Perry Road, Exeter EX4 4QG, United Kingdom.
Plant Cell. 2001 Sep;13(9):1987-2004. doi: 10.1105/tpc.010056.
Plant infection by the rice blast fungus Magnaporthe grisea is brought about by the action of specialized infection cells called appressoria. These infection cells generate enormous turgor pressure, which is translated into an invasive force that allows a narrow penetration hypha to breach the plant cuticle. The Magnaporthe pde1 mutant was identified previously by restriction enzyme-mediated DNA integration mutagenesis and is impaired in its ability to elaborate penetration hyphae. Here we report that the pde1 mutation is the result of an insertion into the promoter of a P-type ATPase-encoding gene. Targeted gene disruption confirmed the role of PDE1 in penetration hypha development and pathogenicity but highlighted potential differences in PDE1 regulation in different Magnaporthe strains. The predicted PDE1 gene product was most similar to members of the aminophospholipid translocase group of P-type ATPases and was shown to be a functional homolog of the yeast ATPase gene ATC8. Spatial expression studies showed that PDE1 is expressed in germinating conidia and developing appressoria. These findings implicate the action of aminophospholipid translocases in the development of penetration hyphae and the proliferation of the fungus beyond colonization of the first epidermal cell.
稻瘟病菌Magnaporthe grisea对植物的感染是由一种称为附着胞的特殊感染细胞的作用引起的。这些感染细胞会产生巨大的膨压,该膨压会转化为一种侵入力,使一条狭窄的穿透菌丝突破植物角质层。Magnaporthe pde1突变体先前是通过限制酶介导的DNA整合诱变鉴定出来的,其形成穿透菌丝的能力受损。在此我们报告,pde1突变是由于插入到一个编码P型ATP酶的基因的启动子中所致。靶向基因破坏证实了PDE1在穿透菌丝发育和致病性中的作用,但也突出了不同Magnaporthe菌株中PDE1调控的潜在差异。预测的PDE1基因产物与P型ATP酶的氨基磷脂转运酶组的成员最为相似,并被证明是酵母ATP酶基因ATC8的功能同源物。空间表达研究表明,PDE1在萌发的分生孢子和发育中的附着胞中表达。这些发现表明氨基磷脂转运酶在穿透菌丝的发育以及真菌在第一个表皮细胞定殖后的增殖过程中发挥作用。