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Genome sequence of the model medicinal mushroom Ganoderma lucidum
Ganoderma lucidum is a widely used medicinal macrofungus in traditional Chinese medicine that creates a diverse set of bioactive compounds. Here we report its 43.3-Mb genome, encoding 16,113 predicted genes, obtained using next-generation sequencing and optical mapping approaches. The sequence analy...
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Published in: | Nature communications 2012-06, Vol.3 (1), p.913-913, Article 913 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Ganoderma lucidum
is a widely used medicinal macrofungus in traditional Chinese medicine that creates a diverse set of bioactive compounds. Here we report its 43.3-Mb genome, encoding 16,113 predicted genes, obtained using next-generation sequencing and optical mapping approaches. The sequence analysis reveals an impressive array of genes encoding cytochrome P450s (CYPs), transporters and regulatory proteins that cooperate in secondary metabolism. The genome also encodes one of the richest sets of wood degradation enzymes among all of the sequenced basidiomycetes. In all, 24 physical CYP gene clusters are identified. Moreover, 78 CYP genes are coexpressed with lanosterol synthase, and 16 of these show high similarity to fungal CYPs that specifically hydroxylate testosterone, suggesting their possible roles in triterpenoid biosynthesis. The elucidation of the
G. lucidum
genome makes this organism a potential model system for the study of secondary metabolic pathways and their regulation in medicinal fungi.
Ganoderma lucidum
is a macrofungus in traditional Chinese medicine known to produce different bioactive compounds. In this study, the genome of
G. lucidum
is sequenced, making this organism a potential model system for future studies of secondary metabolic pathways and their regulation in medicinal fungi. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/ncomms1923 |