Department of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana, United States of America.
PLoS Pathog. 2012 Sep;8(9):e1002911. doi: 10.1371/journal.ppat.1002911. Epub 2012 Sep 6.
Surface recognition and penetration are critical steps in the infection cycle of many plant pathogenic fungi. In Magnaporthe oryzae, cAMP signaling is involved in surface recognition and pathogenesis. Deletion of the MAC1 adenylate cyclase gene affected appressorium formation and plant infection. In this study, we used the affinity purification approach to identify proteins that are associated with Mac1 in vivo. One of the Mac1-interacting proteins is the adenylate cyclase-associated protein named Cap1. CAP genes are well-conserved in phytopathogenic fungi but none of them have been functionally characterized. Deletion of CAP1 blocked the effects of a dominant RAS2 allele and resulted in defects in invasive growth and a reduced intracellular cAMP level. The Δcap1 mutant was defective in germ tube growth, appressorium formation, and formation of typical blast lesions. Cap1-GFP had an actin-like localization pattern, localizing to the apical regions in vegetative hyphae, at the periphery of developing appressoria, and in circular structures at the base of mature appressoria. Interestingly, Cap1, similar to LifeAct, did not localize to the apical regions in invasive hyphae, suggesting that the apical actin cytoskeleton differs between vegetative and invasive hyphae. Domain deletion analysis indicated that the proline-rich region P2 but not the actin-binding domain (AB) of Cap1 was responsible for its subcellular localization. Nevertheless, the AB domain of Cap1 must be important for its function because CAP1(ΔAB) only partially rescued the Δcap1 mutant. Furthermore, exogenous cAMP induced the formation of appressorium-like structures in non-germinated conidia in CAP1(ΔAB) transformants. This novel observation suggested that AB domain deletion may result in overstimulation of appressorium formation by cAMP treatment. Overall, our results indicated that CAP1 is important for the activation of adenylate cyclase, appressorium morphogenesis, and plant infection in M. oryzae. CAP1 may also play a role in feedback inhibition of Ras2 signaling when Pmk1 is activated.
表面识别和穿透是许多植物病原真菌感染周期的关键步骤。在稻瘟病菌中,cAMP 信号参与了表面识别和发病机制。MAC1 腺苷酸环化酶基因的缺失影响了附着胞的形成和植物的侵染。在这项研究中,我们使用亲和纯化的方法来鉴定体内与 Mac1 相互作用的蛋白质。Mac1 相互作用蛋白之一是一种称为 Cap1 的腺苷酸环化酶相关蛋白。CAP 基因在植物病原真菌中高度保守,但它们的功能尚未得到证实。CAP1 的缺失阻断了显性 RAS2 等位基因的作用,并导致了侵袭性生长和细胞内 cAMP 水平降低的缺陷。Δcap1 突变体在芽管生长、附着胞形成和典型的膨泡损伤形成方面存在缺陷。Cap1-GFP 具有与肌动蛋白相似的定位模式,在营养菌丝的顶端区域、发育中的附着胞的外围以及成熟附着胞的基部的环状结构中定位。有趣的是,Cap1 与 LifeAct 相似,不在侵入性菌丝的顶端区域定位,这表明营养菌丝和侵入性菌丝的顶端肌动蛋白细胞骨架不同。结构域缺失分析表明,Cap1 的富含脯氨酸的区域 P2 而不是肌动蛋白结合结构域(AB)负责其亚细胞定位。然而,Cap1 的 AB 结构域对其功能很重要,因为 CAP1(ΔAB)仅部分挽救了 Δcap1 突变体。此外,外源性 cAMP 诱导 CAP1(ΔAB)转化体中非发芽孢子形成类似附着胞的结构。这一新颖的观察结果表明,AB 结构域缺失可能导致 cAMP 处理过度刺激附着胞的形成。总之,我们的结果表明,CAP1 对稻瘟病菌中腺苷酸环化酶的激活、附着胞形态发生和植物侵染很重要。当 Pmk1 被激活时,CAP1 也可能在 Ras2 信号的反馈抑制中发挥作用。