» Articles » PMID: 22904054

Deletion of the Aspergillus Flavus Orthologue of A. Nidulans FluG Reduces Conidiation and Promotes Production of Sclerotia but Does Not Abolish Aflatoxin Biosynthesis

Overview
Date 2012 Aug 21
PMID 22904054
Citations 42
Authors
Affiliations
Soon will be listed here.
Abstract

The fluG gene is a member of a family of genes required for conidiation and sterigmatocystin production in Aspergillus nidulans. We examined the role of the Aspergillus flavus fluG orthologue in asexual development and aflatoxin biosynthesis. Deletion of fluG in A. flavus yielded strains with an approximately 3-fold reduction in conidiation but a 30-fold increase in sclerotial formation when grown on potato dextrose agar in the dark. The concurrent developmental changes suggest that A. flavus FluG exerts opposite effects on a mutual signaling pathway for both processes. The altered conidial development was in part attributable to delayed expression of brlA, a gene controlling conidiophore formation. Unlike the loss of sterigmatocystin production by A. nidulans fluG deletion strains, aflatoxin biosynthesis was not affected by the fluG deletion in A. flavus. In A. nidulans, FluG was recently found to be involved in the formation of dehydroaustinol, a component of a diffusible signal of conidiation. Coculturing experiments did not show a similar diffusible meroterpenoid secondary metabolite produced by A. flavus. These results suggest that the function of fluG and the signaling pathways related to conidiation are different in the two related aspergilli.

Citing Articles

The putative forkhead transcription factor FhpA is necessary for development, aflatoxin production, and stress response in Aspergillus flavus.

Lohmar J, Gross S, Carter-Wientjes C, Mack B, Wei Q, Lebar M PLoS One. 2025; 20(3):e0315766.

PMID: 40029854 PMC: 11875336. DOI: 10.1371/journal.pone.0315766.


Comprehensive Insights into the Remarkable Function and Regulatory Mechanism of FluG during Asexual Development in .

Li F, Zhang J, Zhong H, Yu K, Chen J Int J Mol Sci. 2024; 25(11).

PMID: 38892450 PMC: 11173134. DOI: 10.3390/ijms25116261.


The KdmB-EcoA-RpdA-SntB (KERS) chromatin regulatory complex controls development, secondary metabolism and pathogenicity in Aspergillus flavus.

Karahoda B, Pfannenstiel B, Sarikaya-Bayram O, Dong Z, Wong K, Fleming A Fungal Genet Biol. 2023; 169:103836.

PMID: 37666447 PMC: 10841535. DOI: 10.1016/j.fgb.2023.103836.


Trace copper-mediated asexual development a superoxide dismutase and induction of in .

Katayama T, Maruyama J Front Microbiol. 2023; 14:1135012.

PMID: 36970664 PMC: 10030727. DOI: 10.3389/fmicb.2023.1135012.


Kojic Acid Gene Clusters and the Transcriptional Activation Mechanism of KojR on Expression of Clustered Genes.

Chang P, Scharfenstein L, Mahoney N, Kong Q J Fungi (Basel). 2023; 9(2).

PMID: 36836373 PMC: 9961346. DOI: 10.3390/jof9020259.


References
1.
Galagan J, Calvo S, Cuomo C, Ma L, Wortman J, Batzoglou S . Sequencing of Aspergillus nidulans and comparative analysis with A. fumigatus and A. oryzae. Nature. 2005; 438(7071):1105-15. DOI: 10.1038/nature04341. View

2.
Lee B, Adams T . The Aspergillus nidulans fluG gene is required for production of an extracellular developmental signal and is related to prokaryotic glutamine synthetase I. Genes Dev. 1994; 8(6):641-51. DOI: 10.1101/gad.8.6.641. View

3.
DSouza C, Lee B, Adams T . Characterization of the role of the FluG protein in asexual development of Aspergillus nidulans. Genetics. 2001; 158(3):1027-36. PMC: 1461723. DOI: 10.1093/genetics/158.3.1027. View

4.
Doskocilova A, Plihal O, Volc J, Chumova J, Kourova H, Halada P . A nodulin/glutamine synthetase-like fusion protein is implicated in the regulation of root morphogenesis and in signalling triggered by flagellin. Planta. 2011; 234(3):459-76. DOI: 10.1007/s00425-011-1419-7. View

5.
Kim H, Han K, Kim K, Han D, Jahng K, Chae K . The veA gene activates sexual development in Aspergillus nidulans. Fungal Genet Biol. 2002; 37(1):72-80. DOI: 10.1016/s1087-1845(02)00029-4. View