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Comparative transcriptomics highlights convergent evolution of energy metabolic pathways in group-living spiders
Although widely thought to be aggressive, solitary, and potentially cannibalistic, some spider species have evolved group-living behaviors. The distinct transition provides the framework to uncover group-living evolution. Here, we conducted a comparative transcriptomic study and examined patterns of...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Science Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995277/ https://www.ncbi.nlm.nih.gov/pubmed/33709634 http://dx.doi.org/10.24272/j.issn.2095-8137.2020.281 |
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author | Yang, Han Lyu, Bin Yin, Hai-Qiang Li, Shu-Qiang |
author_facet | Yang, Han Lyu, Bin Yin, Hai-Qiang Li, Shu-Qiang |
author_sort | Yang, Han |
collection | PubMed |
description | Although widely thought to be aggressive, solitary, and potentially cannibalistic, some spider species have evolved group-living behaviors. The distinct transition provides the framework to uncover group-living evolution. Here, we conducted a comparative transcriptomic study and examined patterns of molecular evolution in two independently evolved group-living spiders and twelve solitary species. We report that positively selected genes among group-living spider lineages are significantly enriched in nutrient metabolism and autophagy pathways. We also show that nutrient-related genes of group-living spiders convergently experience amino acid substitutions and accelerated relative evolutionary rates. These results indicate adaptive convergence of nutrient metabolism that may ensure energy supply in group-living spiders. The decelerated evolutionary rate of autophagy-related genes in group-living lineages is consistent with an increased constraint on energy homeostasis as would be required in a group-living environment. Together, the results show that energy metabolic pathways play an important role in the transition to group-living in spiders. |
format | Online Article Text |
id | pubmed-7995277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Science Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79952772021-04-01 Comparative transcriptomics highlights convergent evolution of energy metabolic pathways in group-living spiders Yang, Han Lyu, Bin Yin, Hai-Qiang Li, Shu-Qiang Zool Res Article Although widely thought to be aggressive, solitary, and potentially cannibalistic, some spider species have evolved group-living behaviors. The distinct transition provides the framework to uncover group-living evolution. Here, we conducted a comparative transcriptomic study and examined patterns of molecular evolution in two independently evolved group-living spiders and twelve solitary species. We report that positively selected genes among group-living spider lineages are significantly enriched in nutrient metabolism and autophagy pathways. We also show that nutrient-related genes of group-living spiders convergently experience amino acid substitutions and accelerated relative evolutionary rates. These results indicate adaptive convergence of nutrient metabolism that may ensure energy supply in group-living spiders. The decelerated evolutionary rate of autophagy-related genes in group-living lineages is consistent with an increased constraint on energy homeostasis as would be required in a group-living environment. Together, the results show that energy metabolic pathways play an important role in the transition to group-living in spiders. Science Press 2021-03-18 /pmc/articles/PMC7995277/ /pubmed/33709634 http://dx.doi.org/10.24272/j.issn.2095-8137.2020.281 Text en Editorial Office of Zoological Research, Kunming Institute of Zoology, Chinese Academy of Sciences http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Yang, Han Lyu, Bin Yin, Hai-Qiang Li, Shu-Qiang Comparative transcriptomics highlights convergent evolution of energy metabolic pathways in group-living spiders |
title | Comparative transcriptomics highlights convergent evolution of energy metabolic pathways in group-living spiders |
title_full | Comparative transcriptomics highlights convergent evolution of energy metabolic pathways in group-living spiders |
title_fullStr | Comparative transcriptomics highlights convergent evolution of energy metabolic pathways in group-living spiders |
title_full_unstemmed | Comparative transcriptomics highlights convergent evolution of energy metabolic pathways in group-living spiders |
title_short | Comparative transcriptomics highlights convergent evolution of energy metabolic pathways in group-living spiders |
title_sort | comparative transcriptomics highlights convergent evolution of energy metabolic pathways in group-living spiders |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995277/ https://www.ncbi.nlm.nih.gov/pubmed/33709634 http://dx.doi.org/10.24272/j.issn.2095-8137.2020.281 |
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