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Embryonic muscle splitting patterns reveal homologies of amniote forelimb muscles

Limb muscles are remarkably complex and evolutionarily labile. Although their anatomy is of great interest for studies of the evolution of form and function, their homologies among major amniote clades have remained obscure. Studies of adult musculature are inconclusive owing to the highly derived m...

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Autores principales: Smith-Paredes, Daniel, Vergara-Cereghino, Miccaella E., Lord, Arianna, Moses, Malcolm M., Behringer, Richard R., Bhullar, Bhart-Anjan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090950/
https://www.ncbi.nlm.nih.gov/pubmed/35314784
http://dx.doi.org/10.1038/s41559-022-01699-x
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author Smith-Paredes, Daniel
Vergara-Cereghino, Miccaella E.
Lord, Arianna
Moses, Malcolm M.
Behringer, Richard R.
Bhullar, Bhart-Anjan S.
author_facet Smith-Paredes, Daniel
Vergara-Cereghino, Miccaella E.
Lord, Arianna
Moses, Malcolm M.
Behringer, Richard R.
Bhullar, Bhart-Anjan S.
author_sort Smith-Paredes, Daniel
collection PubMed
description Limb muscles are remarkably complex and evolutionarily labile. Although their anatomy is of great interest for studies of the evolution of form and function, their homologies among major amniote clades have remained obscure. Studies of adult musculature are inconclusive owing to the highly derived morphology of modern amniote limbs, but correspondences become increasingly evident earlier in ontogeny. We followed the embryonic development of forelimb musculature in representatives of six major amniote clades and found, contrary to current consensus, that these early splitting patterns are highly conserved across Amniota. Muscle mass cleavage patterns and topology are highly conserved in reptiles including birds, irrespective of their skeletal modifications: the avian flight apparatus results from slight early topological modifications that are exaggerated during ontogeny. Therian mammals, while conservative in their cleavage patterns, depart drastically from the ancestral amniote musculoskeletal organization in terms of topology. These topological changes occur through extension, translocation, and displacement of muscle groups later in development. Overall, the simplicity underlying the apparent complexity of forelimb muscle development allows us to resolve conflicting hypotheses about homology and to trace the history of each individual forelimb muscle throughout the amniote radiations.
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spelling pubmed-90909502022-09-21 Embryonic muscle splitting patterns reveal homologies of amniote forelimb muscles Smith-Paredes, Daniel Vergara-Cereghino, Miccaella E. Lord, Arianna Moses, Malcolm M. Behringer, Richard R. Bhullar, Bhart-Anjan S. Nat Ecol Evol Article Limb muscles are remarkably complex and evolutionarily labile. Although their anatomy is of great interest for studies of the evolution of form and function, their homologies among major amniote clades have remained obscure. Studies of adult musculature are inconclusive owing to the highly derived morphology of modern amniote limbs, but correspondences become increasingly evident earlier in ontogeny. We followed the embryonic development of forelimb musculature in representatives of six major amniote clades and found, contrary to current consensus, that these early splitting patterns are highly conserved across Amniota. Muscle mass cleavage patterns and topology are highly conserved in reptiles including birds, irrespective of their skeletal modifications: the avian flight apparatus results from slight early topological modifications that are exaggerated during ontogeny. Therian mammals, while conservative in their cleavage patterns, depart drastically from the ancestral amniote musculoskeletal organization in terms of topology. These topological changes occur through extension, translocation, and displacement of muscle groups later in development. Overall, the simplicity underlying the apparent complexity of forelimb muscle development allows us to resolve conflicting hypotheses about homology and to trace the history of each individual forelimb muscle throughout the amniote radiations. 2022-05 2022-03-21 /pmc/articles/PMC9090950/ /pubmed/35314784 http://dx.doi.org/10.1038/s41559-022-01699-x Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms
spellingShingle Article
Smith-Paredes, Daniel
Vergara-Cereghino, Miccaella E.
Lord, Arianna
Moses, Malcolm M.
Behringer, Richard R.
Bhullar, Bhart-Anjan S.
Embryonic muscle splitting patterns reveal homologies of amniote forelimb muscles
title Embryonic muscle splitting patterns reveal homologies of amniote forelimb muscles
title_full Embryonic muscle splitting patterns reveal homologies of amniote forelimb muscles
title_fullStr Embryonic muscle splitting patterns reveal homologies of amniote forelimb muscles
title_full_unstemmed Embryonic muscle splitting patterns reveal homologies of amniote forelimb muscles
title_short Embryonic muscle splitting patterns reveal homologies of amniote forelimb muscles
title_sort embryonic muscle splitting patterns reveal homologies of amniote forelimb muscles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090950/
https://www.ncbi.nlm.nih.gov/pubmed/35314784
http://dx.doi.org/10.1038/s41559-022-01699-x
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