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一种假定的丝裂原活化蛋白激酶激酶激酶MCK1,是稻瘟病菌细胞壁完整性和致病性所必需的。

A putative MAP kinase kinase kinase, MCK1, is required for cell wall integrity and pathogenicity of the rice blast fungus, Magnaporthe oryzae.

作者信息

Jeon Junhyun, Goh Jaeduk, Yoo Sungyong, Chi Myoung-Hwan, Choi Jaehyuk, Rho Hee-Sool, Park Jongsun, Han Seong-Sook, Kim Byeong Ryun, Park Sook-Young, Kim Soonok, Lee Yong-Hwan

机构信息

Department of Agricultural Biotechnology, Center for Fungal Genetic Resources, Seoul National University, Seoul 151-921, Korea.

出版信息

Mol Plant Microbe Interact. 2008 May;21(5):525-34. doi: 10.1094/MPMI-21-5-0525.

Abstract

Insertional mutagenesis of Magnaporthe oryzae led to the identification of MCK1, a pathogenicity gene predicted to encode mitogen-activated protein kinase kinase kinase (MAPKKK) homologous to BCK1 in Saccharomyces cerevisiae. Targeted disruption of MCK1 resulted in the fungus undergoing autolysis and showing hypersensitivity to cell-wall-degrading enzyme. The mck1 produced significantly reduced numbers of conidia and developed appressoria in a slightly retarded manner compared with the wild type. Appressorium of the mck1 mutant was unable to penetrate into plant tissues, thereby rendering the mutant nonpathogenic. Cytorrhysis assay and monitoring of lipid mobilization suggested that the appressorial wall was altered, presumably affecting the level of turgor pressure within appressorium. Furthermore, the mck1 mutant failed to grow inside plant tissue. Complementation of the mutated gene restored its ability to cause disease symptoms, demonstrating that MCK1 is required for fungal pathogenicity. Taken together, our results suggest that MCK1 is an MAPKKK involved in maintaining cell wall integrity of M. oryzae, and that remodeling of the cell wall in response to host environments is essential for fungal pathogenesis.

摘要

稻瘟病菌的插入诱变导致了MCK1的鉴定,MCK1是一个致病基因,预计编码与酿酒酵母中的BCK1同源的丝裂原活化蛋白激酶激酶激酶(MAPKKK)。对MCK1进行靶向破坏导致真菌自溶,并对细胞壁降解酶表现出超敏反应。与野生型相比,mck1产生的分生孢子数量显著减少,附着胞的形成也稍有延迟。mck1突变体的附着胞无法穿透植物组织,从而使该突变体无致病性。细胞解体试验和脂质动员监测表明,附着胞壁发生了改变,可能影响了附着胞内的膨压水平。此外,mck1突变体无法在植物组织内生长。突变基因的互补恢复了其引起疾病症状的能力,表明MCK1是真菌致病性所必需的。综上所述,我们的结果表明,MCK1是一种参与维持稻瘟病菌细胞壁完整性的MAPKKK,并且响应宿主环境的细胞壁重塑对于真菌致病至关重要。

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