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Reciprocal genomic evolution in the ant–fungus agricultural symbiosis

The attine ant–fungus agricultural symbiosis evolved over tens of millions of years, producing complex societies with industrial-scale farming analogous to that of humans. Here we document reciprocal shifts in the genomes and transcriptomes of seven fungus-farming ant species and their fungal cultiv...

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Autores principales: Nygaard, Sanne, Hu, Haofu, Li, Cai, Schiøtt, Morten, Chen, Zhensheng, Yang, Zhikai, Xie, Qiaolin, Ma, Chunyu, Deng, Yuan, Dikow, Rebecca B., Rabeling, Christian, Nash, David R., Wcislo, William T., Brady, Seán G., Schultz, Ted R., Zhang, Guojie, Boomsma, Jacobus J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961791/
https://www.ncbi.nlm.nih.gov/pubmed/27436133
http://dx.doi.org/10.1038/ncomms12233
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author Nygaard, Sanne
Hu, Haofu
Li, Cai
Schiøtt, Morten
Chen, Zhensheng
Yang, Zhikai
Xie, Qiaolin
Ma, Chunyu
Deng, Yuan
Dikow, Rebecca B.
Rabeling, Christian
Nash, David R.
Wcislo, William T.
Brady, Seán G.
Schultz, Ted R.
Zhang, Guojie
Boomsma, Jacobus J.
author_facet Nygaard, Sanne
Hu, Haofu
Li, Cai
Schiøtt, Morten
Chen, Zhensheng
Yang, Zhikai
Xie, Qiaolin
Ma, Chunyu
Deng, Yuan
Dikow, Rebecca B.
Rabeling, Christian
Nash, David R.
Wcislo, William T.
Brady, Seán G.
Schultz, Ted R.
Zhang, Guojie
Boomsma, Jacobus J.
author_sort Nygaard, Sanne
collection PubMed
description The attine ant–fungus agricultural symbiosis evolved over tens of millions of years, producing complex societies with industrial-scale farming analogous to that of humans. Here we document reciprocal shifts in the genomes and transcriptomes of seven fungus-farming ant species and their fungal cultivars. We show that ant subsistence farming probably originated in the early Tertiary (55–60 MYA), followed by further transitions to the farming of fully domesticated cultivars and leaf-cutting, both arising earlier than previously estimated. Evolutionary modifications in the ants include unprecedented rates of genome-wide structural rearrangement, early loss of arginine biosynthesis and positive selection on chitinase pathways. Modifications of fungal cultivars include loss of a key ligninase domain, changes in chitin synthesis and a reduction in carbohydrate-degrading enzymes as the ants gradually transitioned to functional herbivory. In contrast to human farming, increasing dependence on a single cultivar lineage appears to have been essential to the origin of industrial-scale ant agriculture.
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spelling pubmed-49617912016-09-06 Reciprocal genomic evolution in the ant–fungus agricultural symbiosis Nygaard, Sanne Hu, Haofu Li, Cai Schiøtt, Morten Chen, Zhensheng Yang, Zhikai Xie, Qiaolin Ma, Chunyu Deng, Yuan Dikow, Rebecca B. Rabeling, Christian Nash, David R. Wcislo, William T. Brady, Seán G. Schultz, Ted R. Zhang, Guojie Boomsma, Jacobus J. Nat Commun Article The attine ant–fungus agricultural symbiosis evolved over tens of millions of years, producing complex societies with industrial-scale farming analogous to that of humans. Here we document reciprocal shifts in the genomes and transcriptomes of seven fungus-farming ant species and their fungal cultivars. We show that ant subsistence farming probably originated in the early Tertiary (55–60 MYA), followed by further transitions to the farming of fully domesticated cultivars and leaf-cutting, both arising earlier than previously estimated. Evolutionary modifications in the ants include unprecedented rates of genome-wide structural rearrangement, early loss of arginine biosynthesis and positive selection on chitinase pathways. Modifications of fungal cultivars include loss of a key ligninase domain, changes in chitin synthesis and a reduction in carbohydrate-degrading enzymes as the ants gradually transitioned to functional herbivory. In contrast to human farming, increasing dependence on a single cultivar lineage appears to have been essential to the origin of industrial-scale ant agriculture. Nature Publishing Group 2016-07-20 /pmc/articles/PMC4961791/ /pubmed/27436133 http://dx.doi.org/10.1038/ncomms12233 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Nygaard, Sanne
Hu, Haofu
Li, Cai
Schiøtt, Morten
Chen, Zhensheng
Yang, Zhikai
Xie, Qiaolin
Ma, Chunyu
Deng, Yuan
Dikow, Rebecca B.
Rabeling, Christian
Nash, David R.
Wcislo, William T.
Brady, Seán G.
Schultz, Ted R.
Zhang, Guojie
Boomsma, Jacobus J.
Reciprocal genomic evolution in the ant–fungus agricultural symbiosis
title Reciprocal genomic evolution in the ant–fungus agricultural symbiosis
title_full Reciprocal genomic evolution in the ant–fungus agricultural symbiosis
title_fullStr Reciprocal genomic evolution in the ant–fungus agricultural symbiosis
title_full_unstemmed Reciprocal genomic evolution in the ant–fungus agricultural symbiosis
title_short Reciprocal genomic evolution in the ant–fungus agricultural symbiosis
title_sort reciprocal genomic evolution in the ant–fungus agricultural symbiosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961791/
https://www.ncbi.nlm.nih.gov/pubmed/27436133
http://dx.doi.org/10.1038/ncomms12233
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