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Mitogenomic evolutionary rates in bilateria are influenced by parasitic lifestyle and locomotory capacity

The evidence that parasitic animals exhibit elevated mitogenomic evolutionary rates is inconsistent and limited to Arthropoda. Similarly, the evidence that mitogenomic evolution is faster in species with low locomotory capacity is limited to a handful of animal lineages. We hypothesised that these t...

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Autores principales: Jakovlić, Ivan, Zou, Hong, Ye, Tong, Zhang, Hong, Liu, Xiang, Xiang, Chuan-Yu, Wang, Gui-Tang, Zhang, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562372/
https://www.ncbi.nlm.nih.gov/pubmed/37813879
http://dx.doi.org/10.1038/s41467-023-42095-8
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author Jakovlić, Ivan
Zou, Hong
Ye, Tong
Zhang, Hong
Liu, Xiang
Xiang, Chuan-Yu
Wang, Gui-Tang
Zhang, Dong
author_facet Jakovlić, Ivan
Zou, Hong
Ye, Tong
Zhang, Hong
Liu, Xiang
Xiang, Chuan-Yu
Wang, Gui-Tang
Zhang, Dong
author_sort Jakovlić, Ivan
collection PubMed
description The evidence that parasitic animals exhibit elevated mitogenomic evolutionary rates is inconsistent and limited to Arthropoda. Similarly, the evidence that mitogenomic evolution is faster in species with low locomotory capacity is limited to a handful of animal lineages. We hypothesised that these two variables are associated and that locomotory capacity is a major underlying factor driving the elevated rates in parasites. Here, we study the evolutionary rates of mitogenomes of 10,906 bilaterian species classified according to their locomotory capacity and parasitic/free-living life history. In Bilateria, evolutionary rates were by far the highest in endoparasites, much lower in ectoparasites with reduced locomotory capacity and free-living lineages with low locomotory capacity, followed by parasitoids, ectoparasites with high locomotory capacity, and finally micropredatory and free-living lineages. The life history categorisation (parasitism) explained ≈45%, locomotory capacity categorisation explained ≈39%, and together they explained ≈56% of the total variability in evolutionary rates of mitochondrial protein-coding genes in Bilateria. Our findings suggest that these two variables play major roles in calibrating the mitogenomic molecular clock in bilaterian animals.
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spelling pubmed-105623722023-10-11 Mitogenomic evolutionary rates in bilateria are influenced by parasitic lifestyle and locomotory capacity Jakovlić, Ivan Zou, Hong Ye, Tong Zhang, Hong Liu, Xiang Xiang, Chuan-Yu Wang, Gui-Tang Zhang, Dong Nat Commun Article The evidence that parasitic animals exhibit elevated mitogenomic evolutionary rates is inconsistent and limited to Arthropoda. Similarly, the evidence that mitogenomic evolution is faster in species with low locomotory capacity is limited to a handful of animal lineages. We hypothesised that these two variables are associated and that locomotory capacity is a major underlying factor driving the elevated rates in parasites. Here, we study the evolutionary rates of mitogenomes of 10,906 bilaterian species classified according to their locomotory capacity and parasitic/free-living life history. In Bilateria, evolutionary rates were by far the highest in endoparasites, much lower in ectoparasites with reduced locomotory capacity and free-living lineages with low locomotory capacity, followed by parasitoids, ectoparasites with high locomotory capacity, and finally micropredatory and free-living lineages. The life history categorisation (parasitism) explained ≈45%, locomotory capacity categorisation explained ≈39%, and together they explained ≈56% of the total variability in evolutionary rates of mitochondrial protein-coding genes in Bilateria. Our findings suggest that these two variables play major roles in calibrating the mitogenomic molecular clock in bilaterian animals. Nature Publishing Group UK 2023-10-09 /pmc/articles/PMC10562372/ /pubmed/37813879 http://dx.doi.org/10.1038/s41467-023-42095-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jakovlić, Ivan
Zou, Hong
Ye, Tong
Zhang, Hong
Liu, Xiang
Xiang, Chuan-Yu
Wang, Gui-Tang
Zhang, Dong
Mitogenomic evolutionary rates in bilateria are influenced by parasitic lifestyle and locomotory capacity
title Mitogenomic evolutionary rates in bilateria are influenced by parasitic lifestyle and locomotory capacity
title_full Mitogenomic evolutionary rates in bilateria are influenced by parasitic lifestyle and locomotory capacity
title_fullStr Mitogenomic evolutionary rates in bilateria are influenced by parasitic lifestyle and locomotory capacity
title_full_unstemmed Mitogenomic evolutionary rates in bilateria are influenced by parasitic lifestyle and locomotory capacity
title_short Mitogenomic evolutionary rates in bilateria are influenced by parasitic lifestyle and locomotory capacity
title_sort mitogenomic evolutionary rates in bilateria are influenced by parasitic lifestyle and locomotory capacity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562372/
https://www.ncbi.nlm.nih.gov/pubmed/37813879
http://dx.doi.org/10.1038/s41467-023-42095-8
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