MAPKK FgMkk1 of Fusarium graminearum regulates vegetative differentiation, multiple stress response, and virulence via the cell wall integrity and high‐osmolarity glycerol signaling pathways
Mitogen‐activated protein (MAP) kinases play crucial roles in regulating fungal development, growth and pathogenicity, and in responses to the environment. In this study, we characterized a MAP kinase kinase FgMkk1 in Fusarium graminearum, the causal agent of wheat head blight. Phenotypic analyses o...
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Published in | Environmental microbiology Vol. 16; no. 7; pp. 2023 - 2037 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Blackwell Science
01.07.2014
Blackwell Publishing Ltd Blackwell Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Mitogen‐activated protein (MAP) kinases play crucial roles in regulating fungal development, growth and pathogenicity, and in responses to the environment. In this study, we characterized a MAP kinase kinase FgMkk1 in Fusarium graminearum, the causal agent of wheat head blight. Phenotypic analyses of the FgMKK1 mutant (ΔFgMKK1) showed that FgMkk1 is involved in the regulation of hyphal growth, pigmentation, conidiation, deoxynivalenol biosynthesis and virulence of F. graminearum. ΔFgMKK1 also showed increased sensitivity to cell wall‐damaging agents, and to osmotic and oxidative stresses, but exhibited decreased sensitivity to the fungicides iprodione and fludioxonil. In addition, the mutant revealed increased sensitivity to a biocontrol agent, Trichoderma atroviride. Western blot assays revealed that FgMkk1 positively regulates phosphorylation of the MAP kinases Mgv1 and FgOs‐2, the key component in the cell wall integrity (CWI) and high‐osmolarity glycerol (HOG) signalling pathway respectively. Yeast two‐hybrid assay indicated that Mgv1 interacts with a transcription factor FgRlm1. The FgRLM1 mutant (ΔFgRLM1) showed increased sensitivity to cell wall‐damaging agents and exhibited decreased virulence. Taken together, our data indicated that FgMkk1 is an upstream component of Mgv1, and regulates vegetative differentiation, multiple stress response and virulence via the CWI and HOG signalling pathways. FgRlm1 may be a downstream component of Mgv1 in the CWI pathway in F. graminearum. |
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Bibliography: | http://dx.doi.org/10.1111/1462-2920.12334 National Science Foundation - No. 31171881 ArticleID:EMI12334 National Key Basic Research and Development Program - No. 2013CB127802 Fig. S1. Schematic representation of the FgMKK1 and FgRLM1 deletion strategy. (A) FgMKK1 and (B) FgRLM1 are denoted by large gray arrows respectively. Hygromycin resistance cassette (HPH) is denoted by large black arrow. Annealing sites of PCR primers are indicated with arrows (see Supporting Information Table S1 for primer sequences). (C) The 885 bp FgMKK1 and (D) the 925 bp FgRLM1 upstream fragment was used as a probe in the Southern blot hybridization analyses of the respective mutants. Genomic DNA preparations from the wild-type PH-1, ΔFgMKK1, ΔFgMKK1-C, ΔFgRLM1 and ΔFgRLM1-C were digested with NruI or SphI.Fig. S2. Sensitivity of the wild-type PH-1, ΔFgMKK1, ΔFgMKK1-C, ΔFgRLM1 and ΔFgRLM1-C to various stress conditions. Serial dilutions of conidial suspension of each strain were spotted on MM plates amended with each compound at the concentrations described in the figure. ΔFgMKK1and ΔFgRLM1 did not show recognizable changes in sensitivity to these compounds (indicated in the figure) compared to the wild type and the complemented strains. Images were taken after 2 days of incubation at 25°C.Fig. S3. Morphological comparisons of the wild-type PH-1, FgMKK1 deletion mutant (ΔFgMKK1), FgRLM1 deletion mutant (ΔFgRLM1) and their complemented strains (ΔFgMKK1-C and ΔFgRLM1-C) on wheat head medium.Table S1. PCR primers used in this study. Special Fund for Agro-scientific Research in the Public Interest - No. 201303023 istex:D5E402CB77F87FC18EABAAF2BC384795AA1B32B8 China Agriculture Research System - No. CARS-3-1-15 ark:/67375/WNG-JM5SLDQ8-R ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1462-2912 1462-2920 1462-2920 |
DOI: | 10.1111/1462-2920.12334 |