Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1783352549282152448 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6121855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT reynoldshannaht horizontalgeneclustertransferincreasedhallucinogenicmushroomdiversity AT vijayakumarvinod horizontalgeneclustertransferincreasedhallucinogenicmushroomdiversity AT gluckthaleremile horizontalgeneclustertransferincreasedhallucinogenicmushroomdiversity AT korotkinhaileebrynn horizontalgeneclustertransferincreasedhallucinogenicmushroomdiversity AT mathenypatrickbrandon horizontalgeneclustertransferincreasedhallucinogenicmushroomdiversity AT slotjasonc horizontalgeneclustertransferincreasedhallucinogenicmushroomdiversity |