Abstract

Fungal secondary metabolite biosynthesis genes are of major interest due to the pharmacological properties of their products (like mycotoxins and antibiotics). The genome of the plant pathogenic fungus Fusarium graminearum codes for a large number of candidate enzymes involved in secondary metabolite biosynthesis. However, the chemical nature of most enzymatic products of proteins encoded by putative secondary metabolism biosynthetic genes is largely unknown. Based on our analysis we present 67 gene clusters with significant enrichment of predicted secondary metabolism related enzymatic functions. 20 gene clusters with unknown metabolites exhibit strong gene expression correlation in planta and presumably play a role in virulence. Furthermore, the identification of conserved and over-represented putative transcription factor binding sites serves as additional evidence for cluster co-regulation. Orthologous cluster search provided insight into the evolution of secondary metabolism clusters. Some clusters are characteristic for the Fusarium phylum while others show evidence of horizontal gene transfer as orthologs can be found in representatives of the Botrytis or Cochliobolus lineage. The presented candidate clusters provide valuable targets for experimental examination.

Highlights

  • In fungal genomes, genes involved in specific as well as common metabolic pathways have been observed to form tightly linked clusters on the chromosomes [1,2,3,4,5]

  • Screening neighboring genes for functional gene clusters Based on the compositions of experimentally elucidated clusters we scanned for local accumulations of secondary metabolites (SM) signature genes (TPS, polyketide synthetases (PKS), nonribosomal peptide synthetases (NPS), DMATS) and tailoring enzyme genes and performed a functional enrichment analysis of secondary metabolism related functions to determine the significance of the gene clusters

  • A total number of 67 statistically significant (P-value, 0.05, Fisher’s exact test [35]) potential gene clusters presumably involved in secondary metabolite biosynthesis were identified in this way (Figure 1, Table S2)

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Summary

Introduction

Genes involved in specific as well as common metabolic pathways have been observed to form tightly linked clusters on the chromosomes [1,2,3,4,5]. Some of these clustered genes are of major interest and are intensively studied due to the pharmacological properties of the secondary metabolites (SM) resulting from the activities of the gene products. Despite the potential importance concerning human health or economic impact, it is difficult to identify the chemical products associated with fungal gene clusters because many clustered genes are not expressed under laboratory conditions [6,7]. The comparative analysis of SM gene clusters in diverse genomes should give insight into their evolution and origin

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