Evolution and Diversity of Mycotoxin Gene Clusters

A special issue of Toxins (ISSN 2072-6651). This special issue belongs to the section "Mycotoxins".

Deadline for manuscript submissions: closed (31 October 2022) | Viewed by 4669

Special Issue Editor


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Guest Editor
Department of Botany & Nature Protection, University of Warmia & Mazury in Olsztyn, Plac Lodzki 1, Olsztyn 10-957, Poland
Interests: fungi of the genus Fusarium
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Special Issue Information

Dear Colleagues,

Fungal genomes contain a number of highly organized gene clusters that are involved in the production of secondary metabolites. A large proportion of these metabolites can be toxic, mutagenic, and carcinogenic to animals and humans. These harmful metabolites are designated as mycotoxins. The gene clusters involved in mycotoxin production usually contain a backbone gene that encodes the key enzyme that catalyzes mycotoxin synthesis. Among the most frequently found are polyketide synthase (PKS), nonribosomal peptides synthetase (NRPS), terpenes cyclase, or dimethylallyl tryptophan synthetase. Other genes such as those that encode acetyltransferases, methyltransferases, and oxidoreductases modify backbone compounds. Mycotoxin gene clusters can also contain precursor biosynthesis enzymes, transcription factors, and resistance genes responsible for detoxifying enzymes. The increase in complete fungal genome sequencing has given rise to the discovery and investigation of mycotoxin gene clusters from a broad range of fungal taxa. These clusters are recognized as highly dynamic components of fungal genomes, which mostly emerged from rearrangements and/or duplications of native genes. Fungi can also adapt these clusters through lateral gene transfer to evolve increased adaptation to a host environment. Previous phylogenetic studies have proven their divergent distribution in the fungal kingdom, with frequent rearrangements and remarkable nucleotide variation often observed at the strain level. Despite the recent explosion of information in the field of genomics, mycotoxin gene clusters are still poorly sampled, and the evolutionary processes that have shaped their diversity are largely unknown.

This Special Issue will form a collection of articles, including research and review articles, that will contribute to the better knowledge of the evolution and diversity of mycotoxin gene clusters. To reach this highly worthy aim, high-quality original research and review papers are welcome. These papers should cover comparative and evolutionary studies of mycotoxin gene clusters and/or novel bioinformatic methods in their analysis to study the patterns of diversification and neofunctionalization of mycotoxin gene clusters.

Dr. Tomasz Kulik
Guest Editor

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Keywords

  • Mycotoxin gene cluster
  • Horizontal gene transfer
  • Secondary metabolism
  • Evolution
  • Phylogeny

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Published Papers (1 paper)

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Research

13 pages, 1406 KiB  
Article
Evidence of the Involvement of a Cyclase Gene in the Biosynthesis of Ochratoxin A in Aspergillus carbonarius
by Massimo Ferrara, Antonia Gallo, Carla Cervini, Lucia Gambacorta, Michele Solfrizzo, Scott E. Baker and Giancarlo Perrone
Toxins 2021, 13(12), 892; https://doi.org/10.3390/toxins13120892 - 13 Dec 2021
Cited by 15 | Viewed by 3849
Abstract
Ochratoxin A (OTA) is a well-known mycotoxin with wide distribution in food and feed. Fungal genome sequencing has great utility for identifying secondary metabolites gene clusters for known and novel compounds. A comparative analysis of the OTA-biosynthetic cluster in A. steynii, A. westerdijkiae, [...] Read more.
Ochratoxin A (OTA) is a well-known mycotoxin with wide distribution in food and feed. Fungal genome sequencing has great utility for identifying secondary metabolites gene clusters for known and novel compounds. A comparative analysis of the OTA-biosynthetic cluster in A. steynii, A. westerdijkiae, A. niger, A. carbonarius, and P. nordicum has revealed a high synteny in OTA cluster organization in five structural genes (otaA, otaB, ota, otaR1, and otaD). Moreover, a recent detailed comparative genome analysis of Aspergilli OTA producers led to the identification of a cyclase gene, otaY, located in the OTA cluster between the otaA and otaB genes, encoding for a predicted protein with high similarity to SnoaLs domain. These proteins have been shown to catalyze ring closure steps in the biosynthesis of polyketide antibiotics produced in Streptomyces. In the present study, we demonstrated an upregulation of the cyclase gene in A. carbonarius under OTA permissive conditions, consistent with the expression trends of the other OTA cluster genes and their role in OTA biosynthesis by complete gene deletion. Our results pointed out the involvement of a cyclase gene in OTA biosynthetic pathway for the first time. They represent a step forward in the understanding of the molecular basis of OTA biosynthesis in A. carbonarius. Full article
(This article belongs to the Special Issue Evolution and Diversity of Mycotoxin Gene Clusters)
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