» Articles » PMID: 23874628

Functional Roles of FgLaeA in Controlling Secondary Metabolism, Sexual Development, and Virulence in Fusarium Graminearum

Overview
Journal PLoS One
Date 2013 Jul 23
PMID 23874628
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

Fusarium graminearum, the causal agent of Fusarium head blight in cereal crops, produces mycotoxins such as trichothecenes and zearalenone in infected plants. Here, we focused on the function of FgLaeA in F. graminearum, a homolog of Aspergillus nidulans LaeA encoding the global regulator for both secondary metabolism and sexual development. Prior to gene analysis, we constructed a novel luciferase reporter system consisting of a transgenic F. graminearum strain expressing a firefly luciferase gene under control of the promoter for either TRI6 or ZEB2 controlling the biosynthesis of these mycotoxins. Targeted deletion of FgLaeA led to a dramatic reduction of luminescence in reporter strains, indicating that FgLaeA controls the expression of these transcription factors in F. graminearum; reduced toxin accumulation was further confirmed by GC-MS analysis. Overexpression of FgLaeA caused the increased production of trichothecenes and additional metabolites. RNA seq-analysis revealed that gene member(s) belonging to ~70% of total tentative gene clusters, which were previously proposed, were differentially expressed in the ΔFgLaeA strain. In addition, ΔFgLaeA strains exhibited an earlier induction of sexual fruiting body (perithecia) formation and drastically reduced disease symptoms in wheat, indicating that FgLaeA seems to negatively control perithecial induction, but positively control virulence toward the host plant. FgLaeA was constitutively expressed under both mycotoxin production and sexual development conditions. Overexpression of a GFP-FgLaeA fusion construct in the ΔFgLaeA strain restored all phenotypic changes to wild-type levels and led to constitutive expression of GFP in both nuclei and cytoplasm at different developmental stages. A split luciferase assay demonstrated that FgLaeA was able to interact with FgVeA, a homolog of A. nidulans veA. Taken together, these results demonstrate that FgLaeA, a member of putative FgVeA complex, controls secondary metabolism, sexual development, and virulence in F. graminearum, although the specific regulation pattern differs from that of LaeA in A. nidulans.

Citing Articles

Beyond morphogenesis and secondary metabolism: function of Velvet proteins and LaeA in fungal pathogenesis.

Calvo A, Dabholkar A, Wyman E, Lohmar J, Cary J Appl Environ Microbiol. 2024; 90(10):e0081924.

PMID: 39230285 PMC: 11497805. DOI: 10.1128/aem.00819-24.


Involvement of LaeA and Velvet Proteins in Regulating the Production of Mycotoxins and Other Fungal Secondary Metabolites.

Hou X, Liu L, Xu D, Lai D, Zhou L J Fungi (Basel). 2024; 10(8).

PMID: 39194887 PMC: 11355368. DOI: 10.3390/jof10080561.


Histone H2B lysine 122 and lysine 130, as the putative targets of Penicillium oxalicum LaeA, play important roles in asexual development, expression of secondary metabolite gene clusters, and extracellular glycoside hydrolase synthesis.

Zhang X, Yang Y, Wang L, Qin Y World J Microbiol Biotechnol. 2024; 40(6):179.

PMID: 38668807 DOI: 10.1007/s11274-024-03978-0.


DNA Methylation Is Responsive to the Environment and Regulates the Expression of Biosynthetic Gene Clusters, Metabolite Production, and Virulence in .

Bonner C, Sproule A, Rowland O, Overy D, Subramaniam R Front Fungal Biol. 2023; 1:614633.

PMID: 37743878 PMC: 10512235. DOI: 10.3389/ffunb.2020.614633.


LaeA-Regulated Fungal Traits Mediate Bacterial Community Assembly.

Tannous J, Cosetta C, Drott M, Rush T, Abraham P, Giannone R mBio. 2023; 14(3):e0076923.

PMID: 37162223 PMC: 10294623. DOI: 10.1128/mbio.00769-23.


References
1.
Karimi-Aghcheh R, Bok J, Phatale P, Smith K, Baker S, Lichius A . Functional analyses of Trichoderma reesei LAE1 reveal conserved and contrasting roles of this regulator. G3 (Bethesda). 2013; 3(2):369-78. PMC: 3564997. DOI: 10.1534/g3.112.005140. View

2.
Flaherty J, Pirttila A, Bluhm B, Woloshuk C . PAC1, a pH-regulatory gene from Fusarium verticillioides. Appl Environ Microbiol. 2003; 69(9):5222-7. PMC: 194909. DOI: 10.1128/AEM.69.9.5222-5227.2003. View

3.
ODonnell K, Ward T, Geiser D, Kistler H, Aoki T . Genealogical concordance between the mating type locus and seven other nuclear genes supports formal recognition of nine phylogenetically distinct species within the Fusarium graminearum clade. Fungal Genet Biol. 2004; 41(6):600-23. DOI: 10.1016/j.fgb.2004.03.003. View

4.
Shwab E, Bok J, Tribus M, Galehr J, Graessle S, Keller N . Histone deacetylase activity regulates chemical diversity in Aspergillus. Eukaryot Cell. 2007; 6(9):1656-64. PMC: 2043372. DOI: 10.1128/EC.00186-07. View

5.
Namiki F, Matsunaga M, Okuda M, Inoue I, Nishi K, Fujita Y . Mutation of an arginine biosynthesis gene causes reduced pathogenicity in Fusarium oxysporum f. sp. melonis. Mol Plant Microbe Interact. 2001; 14(4):580-4. DOI: 10.1094/MPMI.2001.14.4.580. View