Cargando…
Fertilization mode differentially impacts the evolution of vertebrate sperm components
Environmental change frequently drives morphological diversification, including at the cellular level. Transitions in the environment where fertilization occurs (i.e., fertilization mode) are hypothesized to be a driver of the extreme diversity in sperm morphology observed in animals. Yet how fertil...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649735/ https://www.ncbi.nlm.nih.gov/pubmed/36357384 http://dx.doi.org/10.1038/s41467-022-34609-7 |
_version_ | 1784827861957345280 |
---|---|
author | Kahrl, Ariel F. Snook, Rhonda R. Fitzpatrick, John L. |
author_facet | Kahrl, Ariel F. Snook, Rhonda R. Fitzpatrick, John L. |
author_sort | Kahrl, Ariel F. |
collection | PubMed |
description | Environmental change frequently drives morphological diversification, including at the cellular level. Transitions in the environment where fertilization occurs (i.e., fertilization mode) are hypothesized to be a driver of the extreme diversity in sperm morphology observed in animals. Yet how fertilization mode impacts the evolution of sperm components—head, midpiece, and flagellum—each with different functional roles that must act as an integrated unit remains unclear. Here, we test this hypothesis by examining the evolution of sperm component lengths across 1103 species of vertebrates varying in fertilization mode (external vs. internal fertilization). Sperm component length is explained in part by fertilization mode across vertebrates, but how fertilization mode influences sperm evolution varies among sperm components and vertebrate clades. We also identify evolutionary responses not influenced by fertilization mode: midpieces evolve rapidly in both external and internal fertilizers. Fertilization mode thus influences vertebrate sperm evolution through complex component- and clade-specific evolutionary responses. |
format | Online Article Text |
id | pubmed-9649735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96497352022-11-15 Fertilization mode differentially impacts the evolution of vertebrate sperm components Kahrl, Ariel F. Snook, Rhonda R. Fitzpatrick, John L. Nat Commun Article Environmental change frequently drives morphological diversification, including at the cellular level. Transitions in the environment where fertilization occurs (i.e., fertilization mode) are hypothesized to be a driver of the extreme diversity in sperm morphology observed in animals. Yet how fertilization mode impacts the evolution of sperm components—head, midpiece, and flagellum—each with different functional roles that must act as an integrated unit remains unclear. Here, we test this hypothesis by examining the evolution of sperm component lengths across 1103 species of vertebrates varying in fertilization mode (external vs. internal fertilization). Sperm component length is explained in part by fertilization mode across vertebrates, but how fertilization mode influences sperm evolution varies among sperm components and vertebrate clades. We also identify evolutionary responses not influenced by fertilization mode: midpieces evolve rapidly in both external and internal fertilizers. Fertilization mode thus influences vertebrate sperm evolution through complex component- and clade-specific evolutionary responses. Nature Publishing Group UK 2022-11-10 /pmc/articles/PMC9649735/ /pubmed/36357384 http://dx.doi.org/10.1038/s41467-022-34609-7 Text en © The Author(s) 2022 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 Kahrl, Ariel F. Snook, Rhonda R. Fitzpatrick, John L. Fertilization mode differentially impacts the evolution of vertebrate sperm components |
title | Fertilization mode differentially impacts the evolution of vertebrate sperm components |
title_full | Fertilization mode differentially impacts the evolution of vertebrate sperm components |
title_fullStr | Fertilization mode differentially impacts the evolution of vertebrate sperm components |
title_full_unstemmed | Fertilization mode differentially impacts the evolution of vertebrate sperm components |
title_short | Fertilization mode differentially impacts the evolution of vertebrate sperm components |
title_sort | fertilization mode differentially impacts the evolution of vertebrate sperm components |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649735/ https://www.ncbi.nlm.nih.gov/pubmed/36357384 http://dx.doi.org/10.1038/s41467-022-34609-7 |
work_keys_str_mv | AT kahrlarielf fertilizationmodedifferentiallyimpactstheevolutionofvertebratespermcomponents AT snookrhondar fertilizationmodedifferentiallyimpactstheevolutionofvertebratespermcomponents AT fitzpatrickjohnl fertilizationmodedifferentiallyimpactstheevolutionofvertebratespermcomponents |