Sakaguchi Ayumu, Miyaji Toshihiko, Tsuji Gento, Kubo Yasuyuki
Laboratory of Plant Pathology, Graduate School of Agriculture, Kyoto Prefectural University, Kyoto 606-8522, Japan.
Eukaryot Cell. 2008 Jan;7(1):102-11. doi: 10.1128/EC.00227-07. Epub 2007 Nov 26.
Kelch repeat proteins are important mediators of fundamental cellular functions and are found in diverse organisms. However, the roles of these proteins in filamentous fungi have not been characterized. We isolated a kelch repeat-encoding gene of Colletotrichum lagenarium ClaKEL2, a Schizosaccharomyces pombe tea1 homologue. Analysis of the clakel2 mutant indicated that ClaKEL2 was required for the establishment of cellular polarity essential for proper morphogenesis of appressoria and that there is a plant signal-specific bypass pathway for appressorium development which circumvents ClaKEL2 function. Clakel2p was localized in the polarized region of growing hyphae and germ tubes, and the localization was disturbed by a microtubule assembly blocker. The clakel2 mutants formed abnormal appressoria, and those appressoria were defective in penetration hypha development into cellulose membranes, an artificial model substrate for fungal infection. Surprisingly, the clakel2 mutants formed normal appressoria on the host plant and retained penetration ability. Normal appressorium formation on the artificial substrate by the clakel2 mutants was restored when cells were incubated in the presence of CaCl(2) or exudates from cucumber cotyledon. Furthermore, calcium channel modulators inhibited restoration of normal appressorium formation. These results suggest that there could be a bypass pathway that transduces a plant-derived signal for appressorium development independent of ClaKEL2 and that a calcium signal is involved in this transduction pathway.
kelch重复蛋白是基本细胞功能的重要调节因子,存在于多种生物中。然而,这些蛋白在丝状真菌中的作用尚未得到表征。我们分离出了瓜类炭疽菌ClaKEL2的一个kelch重复编码基因,它是粟酒裂殖酵母tea1的同源物。对clakel2突变体的分析表明,ClaKEL2是附着胞正常形态发生所必需的细胞极性建立所必需的,并且存在一条植物信号特异性的附着胞发育旁路途径,该途径绕过ClaKEL2的功能。Clakel2p定位于生长菌丝和芽管的极化区域,并且该定位受到微管组装阻断剂的干扰。clakel2突变体形成异常附着胞,并且那些附着胞在穿透菌丝发育进入纤维素膜(一种真菌感染的人工模型底物)方面存在缺陷。令人惊讶的是,clakel2突变体在宿主植物上形成正常附着胞并保留穿透能力。当细胞在氯化钙或黄瓜子叶渗出物存在下培养时,clakel2突变体在人工底物上的正常附着胞形成得以恢复。此外,钙通道调节剂抑制正常附着胞形成的恢复。这些结果表明,可能存在一条旁路途径,该途径转导来自植物的附着胞发育信号而不依赖于ClaKEL2,并且钙信号参与了该转导途径。