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Peer-reviewedCC BY 4.0G3: Genes | Genomes | Genetics

Genomic characterization of the endangered medicinal polypore agarikon (Laricifomes officinalis syn. Fomitopsis officinalis)

Abstract

Agarikon (Laricifomes officinalis syn. Fomitopsis officinalis) is an endangered fungus belonging to a unique lineage in the Polyporales (Basidiomycota) with a growing body of evidence supporting its medicinal value. In this study, we report the hybrid de novo assembly and annotation of the nuclear and mitochondrial genomes of L. officinalis, with a nuclear genome size of 28.76 Mb assembled across 66 contigs (51.96% GC content; BUSCO completeness of 99.4%) and a complete core mitochondrial genome size of 197.67 kb. Structural and functional annotation of the nuclear genome yielded 8,717 predicted genes including 8,604 protein-coding genes, with 287 genes in 27 candidate biosynthetic gene clusters. We characterized the mating type loci matA and matB, consistent with a tetrapolar mating system, and identified genes encoding key enzymes involved in triterpenoid and polyketide biosynthetic pathways that lead to the production of a diverse array of secondary metabolites. Additionally, we conducted maximum likelihood phylogenomic analysis to confirm the taxonomic position of L. officinalis among other species in the Polyporales using protein sequences for 730 shared BUSCO genes. This high-quality annotated genome of L. officinalis will serve as a foundation for further investigations into its evolutionary history, provide a reference for future population genomic analyses, and elucidate mechanisms underlying the synthesis of the bioactive compounds responsible for agarikon's wide-ranging medicinal benefits.

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BibTeX
@article{bennett2026genomic,
  title = {{Genomic characterization of the endangered medicinal polypore agarikon (Laricifomes officinalis syn. Fomitopsis officinalis)}},
  author = {Patrick I Bennett and Zolton J Bair and Alexander J Bradshaw and Paul Stamets},
  journal = {G3: Genes | Genomes | Genetics},
  year = {2026},
  month = aug,
  doi = {10.1093/g3journal/jkag237},
  url = {https://doi.org/10.1093/g3journal/jkag237},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Genomic characterization of the endangered medicinal polypore agarikon (Laricifomes officinalis syn. Fomitopsis officinalis)
AU  - Patrick I Bennett
AU  - Zolton J Bair
AU  - Alexander J Bradshaw
AU  - Paul Stamets
PY  - 2026
DA  - 2026/08/25
JO  - G3: Genes | Genomes | Genetics
DO  - 10.1093/g3journal/jkag237
UR  - https://doi.org/10.1093/g3journal/jkag237
AB  - Agarikon (Laricifomes officinalis syn. Fomitopsis officinalis) is an endangered fungus belonging to a unique lineage in the Polyporales (Basidiomycota) with a growing body of evidence supporting its medicinal value. In this study, we report the hybrid de novo assembly and annotation of the nuclear and mitochondrial genomes of L. officinalis, with a nuclear genome size of 28.76 Mb assembled across 66 contigs (51.96% GC content; BUSCO completeness of 99.4%) and a complete core mitochondrial genome size of 197.67 kb. Structural and functional annotation of the nuclear genome yielded 8,717 predicted genes including 8,604 protein-coding genes, with 287 genes in 27 candidate biosynthetic gene clusters. We characterized the mating type loci matA and matB, consistent with a tetrapolar mating system, and identified genes encoding key enzymes involved in triterpenoid and polyketide biosynthetic pathways that lead to the production of a diverse array of secondary metabolites. Additionally, we conducted maximum likelihood phylogenomic analysis to confirm the taxonomic position of L. officinalis among other species in the Polyporales using protein sequences for 730 shared BUSCO genes. This high-quality annotated genome of L. officinalis will serve as a foundation for further investigations into its evolutionary history, provide a reference for future population genomic analyses, and elucidate mechanisms underlying the synthesis of the bioactive compounds responsible for agarikon's wide-ranging medicinal benefits.
SN  - 2160-1836
ER  -