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Comparative genomics reveals the origin of fungal hyphae and multicellularity
Hyphae represent a hallmark structure of multicellular fungi. The evolutionary origins of hyphae and of the underlying genes are, however, hardly known. By systematically analyzing 72 complete genomes, we here show that hyphae evolved early in fungal evolution probably via diverse genetic changes, i...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733946/ https://www.ncbi.nlm.nih.gov/pubmed/31501435 http://dx.doi.org/10.1038/s41467-019-12085-w |
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author | Kiss, Enikő Hegedüs, Botond Virágh, Máté Varga, Torda Merényi, Zsolt Kószó, Tamás Bálint, Balázs Prasanna, Arun N. Krizsán, Krisztina Kocsubé, Sándor Riquelme, Meritxell Takeshita, Norio Nagy, László G. |
author_facet | Kiss, Enikő Hegedüs, Botond Virágh, Máté Varga, Torda Merényi, Zsolt Kószó, Tamás Bálint, Balázs Prasanna, Arun N. Krizsán, Krisztina Kocsubé, Sándor Riquelme, Meritxell Takeshita, Norio Nagy, László G. |
author_sort | Kiss, Enikő |
collection | PubMed |
description | Hyphae represent a hallmark structure of multicellular fungi. The evolutionary origins of hyphae and of the underlying genes are, however, hardly known. By systematically analyzing 72 complete genomes, we here show that hyphae evolved early in fungal evolution probably via diverse genetic changes, including co-option and exaptation of ancient eukaryotic (e.g. phagocytosis-related) genes, the origin of new gene families, gene duplications and alterations of gene structure, among others. Contrary to most multicellular lineages, the origin of filamentous fungi did not correlate with expansions of kinases, receptors or adhesive proteins. Co-option was probably the dominant mechanism for recruiting genes for hypha morphogenesis, while gene duplication was apparently less prevalent, except in transcriptional regulators and cell wall - related genes. We identified 414 novel gene families that show correlated evolution with hyphae and that may have contributed to its evolution. Our results suggest that hyphae represent a unique multicellular organization that evolved by limited fungal-specific innovations and gene duplication but pervasive co-option and modification of ancient eukaryotic functions. |
format | Online Article Text |
id | pubmed-6733946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67339462019-09-11 Comparative genomics reveals the origin of fungal hyphae and multicellularity Kiss, Enikő Hegedüs, Botond Virágh, Máté Varga, Torda Merényi, Zsolt Kószó, Tamás Bálint, Balázs Prasanna, Arun N. Krizsán, Krisztina Kocsubé, Sándor Riquelme, Meritxell Takeshita, Norio Nagy, László G. Nat Commun Article Hyphae represent a hallmark structure of multicellular fungi. The evolutionary origins of hyphae and of the underlying genes are, however, hardly known. By systematically analyzing 72 complete genomes, we here show that hyphae evolved early in fungal evolution probably via diverse genetic changes, including co-option and exaptation of ancient eukaryotic (e.g. phagocytosis-related) genes, the origin of new gene families, gene duplications and alterations of gene structure, among others. Contrary to most multicellular lineages, the origin of filamentous fungi did not correlate with expansions of kinases, receptors or adhesive proteins. Co-option was probably the dominant mechanism for recruiting genes for hypha morphogenesis, while gene duplication was apparently less prevalent, except in transcriptional regulators and cell wall - related genes. We identified 414 novel gene families that show correlated evolution with hyphae and that may have contributed to its evolution. Our results suggest that hyphae represent a unique multicellular organization that evolved by limited fungal-specific innovations and gene duplication but pervasive co-option and modification of ancient eukaryotic functions. Nature Publishing Group UK 2019-09-09 /pmc/articles/PMC6733946/ /pubmed/31501435 http://dx.doi.org/10.1038/s41467-019-12085-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kiss, Enikő Hegedüs, Botond Virágh, Máté Varga, Torda Merényi, Zsolt Kószó, Tamás Bálint, Balázs Prasanna, Arun N. Krizsán, Krisztina Kocsubé, Sándor Riquelme, Meritxell Takeshita, Norio Nagy, László G. Comparative genomics reveals the origin of fungal hyphae and multicellularity |
title | Comparative genomics reveals the origin of fungal hyphae and multicellularity |
title_full | Comparative genomics reveals the origin of fungal hyphae and multicellularity |
title_fullStr | Comparative genomics reveals the origin of fungal hyphae and multicellularity |
title_full_unstemmed | Comparative genomics reveals the origin of fungal hyphae and multicellularity |
title_short | Comparative genomics reveals the origin of fungal hyphae and multicellularity |
title_sort | comparative genomics reveals the origin of fungal hyphae and multicellularity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733946/ https://www.ncbi.nlm.nih.gov/pubmed/31501435 http://dx.doi.org/10.1038/s41467-019-12085-w |
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