2021
DOI: 10.1111/mpp.13059
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CcPmk1 is a regulator of pathogenicity in Cytospora chrysosperma and can be used as a potential target for disease control

Abstract: This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Cited by 13 publications
(16 citation statements)
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“…Functional annotation of these 12 proteins (except CcPmk1) revealed that 8 out of the 12 were annotated as hypothetical proteins ( Table 1 ). Remarkably, GME3434_g and GME3439_g, annotated as oxidereductase and 1-aminocyclopropane-1-carboxylate oxidase, respectively, were predicted to be translated from genes related to secondary metabolism in our previous study, and these genes are also transcriptionally regulated by CcPmk1 ( 26 ).…”
Section: Resultsmentioning
confidence: 82%
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“…Functional annotation of these 12 proteins (except CcPmk1) revealed that 8 out of the 12 were annotated as hypothetical proteins ( Table 1 ). Remarkably, GME3434_g and GME3439_g, annotated as oxidereductase and 1-aminocyclopropane-1-carboxylate oxidase, respectively, were predicted to be translated from genes related to secondary metabolism in our previous study, and these genes are also transcriptionally regulated by CcPmk1 ( 26 ).…”
Section: Resultsmentioning
confidence: 82%
“…For example, deletion of the Pmk1 ortholog in F. graminearum and Fusarium verticillioides significantly reduced the production of deoxynivalenol and fumonisin, which are important for fungal pathogenicity ( 23 , 24 ). In C. chrysosperma , CcPmk1 can also regulate the expression of genes suggested to be involved in secondary metabolism, as shown by transcriptional analysis ( 26 ). Here, we were surprised to find that CcPmk1 could affect the phosphorylation of GME3434_g and GME3439_g, which are related to secondary metabolism.…”
Section: Discussionmentioning
confidence: 99%
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“…Currently, studies about C. chrysosperma are focused on the taxonomy, genetic diversity, histopathology, and gene function survey [3,4,6,7], while the molecular mechanism studies were few reported. For example, the mitogen-activated protein kinase (CcPmk1) and oxalic acid metabolism were required for the growth and virulence of C. chrysosperma [5,8,9]. The virulence effector CcCAP1, a member of the CAP superfamily (cysteine-rich secretory protein, antigen 5, and pathogenesis-related 1), from C. chrysosperma mainly localized to plant nucleus to suppress plants immune responses [2].…”
Section: Introductionmentioning
confidence: 99%