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Horizontal gene cluster transfer increased hallucinogenic mushroom diversity

Secondary metabolites are a heterogeneous class of chemicals that often mediate interactions between species. The tryptophan‐derived secondary metabolite, psilocin, is a serotonin receptor agonist that induces altered states of consciousness. A phylogenetically disjunct group of mushroom‐forming fun...

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Autores principales: Reynolds, Hannah T., Vijayakumar, Vinod, Gluck‐Thaler, Emile, Korotkin, Hailee Brynn, Matheny, Patrick Brandon, Slot, Jason C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121855/
https://www.ncbi.nlm.nih.gov/pubmed/30283667
http://dx.doi.org/10.1002/evl3.42
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author Reynolds, Hannah T.
Vijayakumar, Vinod
Gluck‐Thaler, Emile
Korotkin, Hailee Brynn
Matheny, Patrick Brandon
Slot, Jason C.
author_facet Reynolds, Hannah T.
Vijayakumar, Vinod
Gluck‐Thaler, Emile
Korotkin, Hailee Brynn
Matheny, Patrick Brandon
Slot, Jason C.
author_sort Reynolds, Hannah T.
collection PubMed
description Secondary metabolites are a heterogeneous class of chemicals that often mediate interactions between species. The tryptophan‐derived secondary metabolite, psilocin, is a serotonin receptor agonist that induces altered states of consciousness. A phylogenetically disjunct group of mushroom‐forming fungi in the Agaricales produce the psilocin prodrug, psilocybin. Spotty phylogenetic distributions of fungal compounds are sometimes explained by horizontal transfer of metabolic gene clusters among unrelated fungi with overlapping niches. We report the discovery of a psilocybin gene cluster in three hallucinogenic mushroom genomes, and evidence for its horizontal transfer between fungal lineages. Patterns of gene distribution and transmission suggest that synthesis of psilocybin may have provided a fitness advantage in the dung and late wood‐decay fungal niches, which may serve as reservoirs of fungal indole‐based metabolites that alter behavior of mycophagous and wood‐eating invertebrates. These hallucinogenic mushroom genomes will serve as models in neurochemical ecology, advancing the (bio)prospecting and synthetic biology of novel neuropharmaceuticals.
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spelling pubmed-61218552018-10-03 Horizontal gene cluster transfer increased hallucinogenic mushroom diversity Reynolds, Hannah T. Vijayakumar, Vinod Gluck‐Thaler, Emile Korotkin, Hailee Brynn Matheny, Patrick Brandon Slot, Jason C. Evol Lett Letters Secondary metabolites are a heterogeneous class of chemicals that often mediate interactions between species. The tryptophan‐derived secondary metabolite, psilocin, is a serotonin receptor agonist that induces altered states of consciousness. A phylogenetically disjunct group of mushroom‐forming fungi in the Agaricales produce the psilocin prodrug, psilocybin. Spotty phylogenetic distributions of fungal compounds are sometimes explained by horizontal transfer of metabolic gene clusters among unrelated fungi with overlapping niches. We report the discovery of a psilocybin gene cluster in three hallucinogenic mushroom genomes, and evidence for its horizontal transfer between fungal lineages. Patterns of gene distribution and transmission suggest that synthesis of psilocybin may have provided a fitness advantage in the dung and late wood‐decay fungal niches, which may serve as reservoirs of fungal indole‐based metabolites that alter behavior of mycophagous and wood‐eating invertebrates. These hallucinogenic mushroom genomes will serve as models in neurochemical ecology, advancing the (bio)prospecting and synthetic biology of novel neuropharmaceuticals. John Wiley and Sons Inc. 2018-02-27 /pmc/articles/PMC6121855/ /pubmed/30283667 http://dx.doi.org/10.1002/evl3.42 Text en © 2018 The Author(s). Evolution Letters published by Wiley Periodicals, Inc. on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB). This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters
Reynolds, Hannah T.
Vijayakumar, Vinod
Gluck‐Thaler, Emile
Korotkin, Hailee Brynn
Matheny, Patrick Brandon
Slot, Jason C.
Horizontal gene cluster transfer increased hallucinogenic mushroom diversity
title Horizontal gene cluster transfer increased hallucinogenic mushroom diversity
title_full Horizontal gene cluster transfer increased hallucinogenic mushroom diversity
title_fullStr Horizontal gene cluster transfer increased hallucinogenic mushroom diversity
title_full_unstemmed Horizontal gene cluster transfer increased hallucinogenic mushroom diversity
title_short Horizontal gene cluster transfer increased hallucinogenic mushroom diversity
title_sort horizontal gene cluster transfer increased hallucinogenic mushroom diversity
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121855/
https://www.ncbi.nlm.nih.gov/pubmed/30283667
http://dx.doi.org/10.1002/evl3.42
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