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Mycena genomes resolve the evolution of fungal bioluminescence

Mushroom-forming fungi in the order Agaricales represent an independent origin of bioluminescence in the tree of life; yet the diversity, evolutionary history, and timing of the origin of fungal luciferases remain elusive. We sequenced the genomes and transcriptomes of five bonnet mushroom species (...

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Autores principales: Ke, Huei-Mien, Lee, Hsin-Han, Lin, Chan-Yi Ivy, Liu, Yu-Ching, Lu, Min R., Hsieh, Jo-Wei Allison, Chang, Chiung-Chih, Wu, Pei-Hsuan, Lu, Meiyeh Jade, Li, Jeng-Yi, Shang, Gaus, Lu, Rita Jui-Hsien, Nagy, László G., Chen, Pao-Yang, Kao, Hsiao-Wei, Tsai, Isheng Jason
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7733832/
https://www.ncbi.nlm.nih.gov/pubmed/33229585
http://dx.doi.org/10.1073/pnas.2010761117
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author Ke, Huei-Mien
Lee, Hsin-Han
Lin, Chan-Yi Ivy
Liu, Yu-Ching
Lu, Min R.
Hsieh, Jo-Wei Allison
Chang, Chiung-Chih
Wu, Pei-Hsuan
Lu, Meiyeh Jade
Li, Jeng-Yi
Shang, Gaus
Lu, Rita Jui-Hsien
Nagy, László G.
Chen, Pao-Yang
Kao, Hsiao-Wei
Tsai, Isheng Jason
author_facet Ke, Huei-Mien
Lee, Hsin-Han
Lin, Chan-Yi Ivy
Liu, Yu-Ching
Lu, Min R.
Hsieh, Jo-Wei Allison
Chang, Chiung-Chih
Wu, Pei-Hsuan
Lu, Meiyeh Jade
Li, Jeng-Yi
Shang, Gaus
Lu, Rita Jui-Hsien
Nagy, László G.
Chen, Pao-Yang
Kao, Hsiao-Wei
Tsai, Isheng Jason
author_sort Ke, Huei-Mien
collection PubMed
description Mushroom-forming fungi in the order Agaricales represent an independent origin of bioluminescence in the tree of life; yet the diversity, evolutionary history, and timing of the origin of fungal luciferases remain elusive. We sequenced the genomes and transcriptomes of five bonnet mushroom species (Mycena spp.), a diverse lineage comprising the majority of bioluminescent fungi. Two species with haploid genome assemblies ∼150 Mb are among the largest in Agaricales, and we found that a variety of repeats between Mycena species were differentially mediated by DNA methylation. We show that bioluminescence evolved in the last common ancestor of mycenoid and the marasmioid clade of Agaricales and was maintained through at least 160 million years of evolution. Analyses of synteny across genomes of bioluminescent species resolved how the luciferase cluster was derived by duplication and translocation, frequently rearranged and lost in most Mycena species, but conserved in the Armillaria lineage. Luciferase cluster members were coexpressed across developmental stages, with the highest expression in fruiting body caps and stipes, suggesting fruiting-related adaptive functions. Our results contribute to understanding a de novo origin of bioluminescence and the corresponding gene cluster in a diverse group of enigmatic fungal species.
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spelling pubmed-77338322020-12-21 Mycena genomes resolve the evolution of fungal bioluminescence Ke, Huei-Mien Lee, Hsin-Han Lin, Chan-Yi Ivy Liu, Yu-Ching Lu, Min R. Hsieh, Jo-Wei Allison Chang, Chiung-Chih Wu, Pei-Hsuan Lu, Meiyeh Jade Li, Jeng-Yi Shang, Gaus Lu, Rita Jui-Hsien Nagy, László G. Chen, Pao-Yang Kao, Hsiao-Wei Tsai, Isheng Jason Proc Natl Acad Sci U S A Biological Sciences Mushroom-forming fungi in the order Agaricales represent an independent origin of bioluminescence in the tree of life; yet the diversity, evolutionary history, and timing of the origin of fungal luciferases remain elusive. We sequenced the genomes and transcriptomes of five bonnet mushroom species (Mycena spp.), a diverse lineage comprising the majority of bioluminescent fungi. Two species with haploid genome assemblies ∼150 Mb are among the largest in Agaricales, and we found that a variety of repeats between Mycena species were differentially mediated by DNA methylation. We show that bioluminescence evolved in the last common ancestor of mycenoid and the marasmioid clade of Agaricales and was maintained through at least 160 million years of evolution. Analyses of synteny across genomes of bioluminescent species resolved how the luciferase cluster was derived by duplication and translocation, frequently rearranged and lost in most Mycena species, but conserved in the Armillaria lineage. Luciferase cluster members were coexpressed across developmental stages, with the highest expression in fruiting body caps and stipes, suggesting fruiting-related adaptive functions. Our results contribute to understanding a de novo origin of bioluminescence and the corresponding gene cluster in a diverse group of enigmatic fungal species. National Academy of Sciences 2020-12-08 2020-11-23 /pmc/articles/PMC7733832/ /pubmed/33229585 http://dx.doi.org/10.1073/pnas.2010761117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Ke, Huei-Mien
Lee, Hsin-Han
Lin, Chan-Yi Ivy
Liu, Yu-Ching
Lu, Min R.
Hsieh, Jo-Wei Allison
Chang, Chiung-Chih
Wu, Pei-Hsuan
Lu, Meiyeh Jade
Li, Jeng-Yi
Shang, Gaus
Lu, Rita Jui-Hsien
Nagy, László G.
Chen, Pao-Yang
Kao, Hsiao-Wei
Tsai, Isheng Jason
Mycena genomes resolve the evolution of fungal bioluminescence
title Mycena genomes resolve the evolution of fungal bioluminescence
title_full Mycena genomes resolve the evolution of fungal bioluminescence
title_fullStr Mycena genomes resolve the evolution of fungal bioluminescence
title_full_unstemmed Mycena genomes resolve the evolution of fungal bioluminescence
title_short Mycena genomes resolve the evolution of fungal bioluminescence
title_sort mycena genomes resolve the evolution of fungal bioluminescence
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7733832/
https://www.ncbi.nlm.nih.gov/pubmed/33229585
http://dx.doi.org/10.1073/pnas.2010761117
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