The resulting framework prioritises reproducible candidates while reserving chemical identity, expression and ecological function for direct validation in basidiomycetes to obscure pathway-centred conservation in basidiomycetes.
Abstract
Fungal biosynthetic gene clusters (BGCs) offer a genomic entry point for natural-product discovery, but predicted regions alone neither establish pathway activity nor identify metabolites. Armillaria is a useful model because chemically rich, forest-associated species span pathogenic and saprotrophic lifestyles. We analysed nine assemblies in a role-aware design: seven independent taxa with high completeness assessed using Benchmarking Universal Single-Copy Orthologs (BUSCO), an A. mellea BUSCO duplication-sensitivity sample and an A. solidipes intraspecific strain control for A. ostoyae. The analysis resolved a terpene-rich repertoire containing a shared but edge-robust gene cluster family (GCF) component alongside unevenly distributed candidate families. Targeted neighbourhood analysis recovered protoilludene synthase (PRO1) orthologs in all assemblies (92.2–100.0% amino-acid identity); the core neighbourhood was retained across the seven primary taxa, whereas flanking tailoring-associated genes varied. Notably, the A. gallica PRO1 ortholog lay 23,614 bp outside the nearest antiSMASH region. Thus, whole-region prediction can obscure pathway-centred conservation in basidiomycetes. The resulting framework prioritises reproducible candidates while reserving chemical identity, expression and ecological function for direct validation.
Comparative genomic and biosynthetic analyses of 24 Talaromyces species reveal extensive diversification alongside selective conservation of secondary-metabolite pathways across Talaromyces and provide a genomic framework for prioritizing species and BGCs for antifungal natural-product discovery and biocontrol-oriented...
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The isolation of a novel Jiangella strain reported from a marine, animal-associated plastisphere is described and its biosynthetic repertoire is placed in the context of the whole genus, providing a genome-based prioritization of candidate biosynthetic targets.
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The new release of BGC Atlas v2 provides taxonomic assignments for nearly all BGCs, harmonized environmental metadata, nested searches across biosynthetic, taxonomic, environmental and geographic properties, and protein-sequence searches against BGC-encoded genes.
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