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Metabolic novelty originating from horizontal gene transfer is essential for leaf beetle survival

Horizontal gene transfer (HGT) provides an evolutionary shortcut for recipient organisms to gain novel functions. Although reports of HGT in higher eukaryotes are rapidly accumulating, in most cases the evolutionary trajectory, metabolic integration, and ecological relevance of acquired genes remain...

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Autores principales: Kirsch, Roy, Okamura, Yu, Haeger, Wiebke, Vogel, Heiko, Kunert, Grit, Pauchet, Yannick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546569/
https://www.ncbi.nlm.nih.gov/pubmed/36161953
http://dx.doi.org/10.1073/pnas.2205857119
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author Kirsch, Roy
Okamura, Yu
Haeger, Wiebke
Vogel, Heiko
Kunert, Grit
Pauchet, Yannick
author_facet Kirsch, Roy
Okamura, Yu
Haeger, Wiebke
Vogel, Heiko
Kunert, Grit
Pauchet, Yannick
author_sort Kirsch, Roy
collection PubMed
description Horizontal gene transfer (HGT) provides an evolutionary shortcut for recipient organisms to gain novel functions. Although reports of HGT in higher eukaryotes are rapidly accumulating, in most cases the evolutionary trajectory, metabolic integration, and ecological relevance of acquired genes remain unclear. Plant cell wall degradation by HGT-derived enzymes is widespread in herbivorous insect lineages. Pectin is an abundant polysaccharide in the walls of growing parts of plants. We investigated the significance of horizontally acquired pectin-digesting polygalacturonases (PGs) of the leaf beetle Phaedon cochleariae. Using a CRISPR/Cas9-guided gene knockout approach, we generated a triple knockout and a quadruple PG-null mutant in order to investigate the enzymatic, biological, and ecological effects. We found that pectin-digestion 1) is exclusively linked to the horizontally acquired PGs from fungi, 2) became fixed in the host genome by gene duplication leading to functional redundancy, 3) compensates for nutrient-poor diet by making the nutritious cell contents more accessible, and 4) facilitates the beetles development and survival. Our analysis highlights the selective advantage PGs provide to herbivorous insects and demonstrate the impact of HGT on the evolutionary success of leaf-feeding beetles, major contributors to species diversity.
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spelling pubmed-95465692022-10-08 Metabolic novelty originating from horizontal gene transfer is essential for leaf beetle survival Kirsch, Roy Okamura, Yu Haeger, Wiebke Vogel, Heiko Kunert, Grit Pauchet, Yannick Proc Natl Acad Sci U S A Biological Sciences Horizontal gene transfer (HGT) provides an evolutionary shortcut for recipient organisms to gain novel functions. Although reports of HGT in higher eukaryotes are rapidly accumulating, in most cases the evolutionary trajectory, metabolic integration, and ecological relevance of acquired genes remain unclear. Plant cell wall degradation by HGT-derived enzymes is widespread in herbivorous insect lineages. Pectin is an abundant polysaccharide in the walls of growing parts of plants. We investigated the significance of horizontally acquired pectin-digesting polygalacturonases (PGs) of the leaf beetle Phaedon cochleariae. Using a CRISPR/Cas9-guided gene knockout approach, we generated a triple knockout and a quadruple PG-null mutant in order to investigate the enzymatic, biological, and ecological effects. We found that pectin-digestion 1) is exclusively linked to the horizontally acquired PGs from fungi, 2) became fixed in the host genome by gene duplication leading to functional redundancy, 3) compensates for nutrient-poor diet by making the nutritious cell contents more accessible, and 4) facilitates the beetles development and survival. Our analysis highlights the selective advantage PGs provide to herbivorous insects and demonstrate the impact of HGT on the evolutionary success of leaf-feeding beetles, major contributors to species diversity. National Academy of Sciences 2022-09-26 2022-10-04 /pmc/articles/PMC9546569/ /pubmed/36161953 http://dx.doi.org/10.1073/pnas.2205857119 Text en Copyright © 2022 the Author(s). Published by PNAS https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Kirsch, Roy
Okamura, Yu
Haeger, Wiebke
Vogel, Heiko
Kunert, Grit
Pauchet, Yannick
Metabolic novelty originating from horizontal gene transfer is essential for leaf beetle survival
title Metabolic novelty originating from horizontal gene transfer is essential for leaf beetle survival
title_full Metabolic novelty originating from horizontal gene transfer is essential for leaf beetle survival
title_fullStr Metabolic novelty originating from horizontal gene transfer is essential for leaf beetle survival
title_full_unstemmed Metabolic novelty originating from horizontal gene transfer is essential for leaf beetle survival
title_short Metabolic novelty originating from horizontal gene transfer is essential for leaf beetle survival
title_sort metabolic novelty originating from horizontal gene transfer is essential for leaf beetle survival
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546569/
https://www.ncbi.nlm.nih.gov/pubmed/36161953
http://dx.doi.org/10.1073/pnas.2205857119
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