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Genomic signatures accompanying the dietary shift to phytophagy in polyphagan beetles

BACKGROUND: The diversity and evolutionary success of beetles (Coleoptera) are proposed to be related to the diversity of plants on which they feed. Indeed, the largest beetle suborder, Polyphaga, mostly includes plant eaters among its approximately 315,000 species. In particular, plants defend them...

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Autores principales: Seppey, Mathieu, Ioannidis, Panagiotis, Emerson, Brent C., Pitteloud, Camille, Robinson-Rechavi, Marc, Roux, Julien, Escalona, Hermes E., McKenna, Duane D., Misof, Bernhard, Shin, Seunggwan, Zhou, Xin, Waterhouse, Robert M., Alvarez, Nadir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525341/
https://www.ncbi.nlm.nih.gov/pubmed/31101123
http://dx.doi.org/10.1186/s13059-019-1704-5
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author Seppey, Mathieu
Ioannidis, Panagiotis
Emerson, Brent C.
Pitteloud, Camille
Robinson-Rechavi, Marc
Roux, Julien
Escalona, Hermes E.
McKenna, Duane D.
Misof, Bernhard
Shin, Seunggwan
Zhou, Xin
Waterhouse, Robert M.
Alvarez, Nadir
author_facet Seppey, Mathieu
Ioannidis, Panagiotis
Emerson, Brent C.
Pitteloud, Camille
Robinson-Rechavi, Marc
Roux, Julien
Escalona, Hermes E.
McKenna, Duane D.
Misof, Bernhard
Shin, Seunggwan
Zhou, Xin
Waterhouse, Robert M.
Alvarez, Nadir
author_sort Seppey, Mathieu
collection PubMed
description BACKGROUND: The diversity and evolutionary success of beetles (Coleoptera) are proposed to be related to the diversity of plants on which they feed. Indeed, the largest beetle suborder, Polyphaga, mostly includes plant eaters among its approximately 315,000 species. In particular, plants defend themselves with a diversity of specialized toxic chemicals. These may impose selective pressures that drive genomic diversification and speciation in phytophagous beetles. However, evidence of changes in beetle gene repertoires driven by such interactions remains largely anecdotal and without explicit hypothesis testing. RESULTS: We explore the genomic consequences of beetle-plant trophic interactions by performing comparative gene family analyses across 18 species representative of the two most species-rich beetle suborders. We contrast the gene contents of species from the mostly plant-eating suborder Polyphaga with those of the mainly predatory Adephaga. We find gene repertoire evolution to be more dynamic, with significantly more adaptive lineage-specific expansions, in the more speciose Polyphaga. Testing the specific hypothesis of adaptation to plant feeding, we identify families of enzymes putatively involved in beetle-plant interactions that underwent adaptive expansions in Polyphaga. There is notable support for the selection hypothesis on large gene families for glutathione S-transferase and carboxylesterase detoxification enzymes. CONCLUSIONS: Our explicit modeling of the evolution of gene repertoires across 18 species identifies putative adaptive lineage-specific gene family expansions that accompany the dietary shift towards plants in beetles. These genomic signatures support the popular hypothesis of a key role for interactions with plant chemical defenses, and for plant feeding in general, in driving beetle diversification. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-019-1704-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-65253412019-05-24 Genomic signatures accompanying the dietary shift to phytophagy in polyphagan beetles Seppey, Mathieu Ioannidis, Panagiotis Emerson, Brent C. Pitteloud, Camille Robinson-Rechavi, Marc Roux, Julien Escalona, Hermes E. McKenna, Duane D. Misof, Bernhard Shin, Seunggwan Zhou, Xin Waterhouse, Robert M. Alvarez, Nadir Genome Biol Research BACKGROUND: The diversity and evolutionary success of beetles (Coleoptera) are proposed to be related to the diversity of plants on which they feed. Indeed, the largest beetle suborder, Polyphaga, mostly includes plant eaters among its approximately 315,000 species. In particular, plants defend themselves with a diversity of specialized toxic chemicals. These may impose selective pressures that drive genomic diversification and speciation in phytophagous beetles. However, evidence of changes in beetle gene repertoires driven by such interactions remains largely anecdotal and without explicit hypothesis testing. RESULTS: We explore the genomic consequences of beetle-plant trophic interactions by performing comparative gene family analyses across 18 species representative of the two most species-rich beetle suborders. We contrast the gene contents of species from the mostly plant-eating suborder Polyphaga with those of the mainly predatory Adephaga. We find gene repertoire evolution to be more dynamic, with significantly more adaptive lineage-specific expansions, in the more speciose Polyphaga. Testing the specific hypothesis of adaptation to plant feeding, we identify families of enzymes putatively involved in beetle-plant interactions that underwent adaptive expansions in Polyphaga. There is notable support for the selection hypothesis on large gene families for glutathione S-transferase and carboxylesterase detoxification enzymes. CONCLUSIONS: Our explicit modeling of the evolution of gene repertoires across 18 species identifies putative adaptive lineage-specific gene family expansions that accompany the dietary shift towards plants in beetles. These genomic signatures support the popular hypothesis of a key role for interactions with plant chemical defenses, and for plant feeding in general, in driving beetle diversification. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-019-1704-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-17 /pmc/articles/PMC6525341/ /pubmed/31101123 http://dx.doi.org/10.1186/s13059-019-1704-5 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Seppey, Mathieu
Ioannidis, Panagiotis
Emerson, Brent C.
Pitteloud, Camille
Robinson-Rechavi, Marc
Roux, Julien
Escalona, Hermes E.
McKenna, Duane D.
Misof, Bernhard
Shin, Seunggwan
Zhou, Xin
Waterhouse, Robert M.
Alvarez, Nadir
Genomic signatures accompanying the dietary shift to phytophagy in polyphagan beetles
title Genomic signatures accompanying the dietary shift to phytophagy in polyphagan beetles
title_full Genomic signatures accompanying the dietary shift to phytophagy in polyphagan beetles
title_fullStr Genomic signatures accompanying the dietary shift to phytophagy in polyphagan beetles
title_full_unstemmed Genomic signatures accompanying the dietary shift to phytophagy in polyphagan beetles
title_short Genomic signatures accompanying the dietary shift to phytophagy in polyphagan beetles
title_sort genomic signatures accompanying the dietary shift to phytophagy in polyphagan beetles
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525341/
https://www.ncbi.nlm.nih.gov/pubmed/31101123
http://dx.doi.org/10.1186/s13059-019-1704-5
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