Cargando…
Cartilage diversification and modularity drove the evolution of the ancestral vertebrate head skeleton
The vertebrate head skeleton has evolved a myriad of forms since their divergence from invertebrate chordates. The connection between novel gene expression and cell types is therefore of importance in this process. The transformation of the jawed vertebrate (gnathostome) head skeleton from oral cirr...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161429/ https://www.ncbi.nlm.nih.gov/pubmed/37147719 http://dx.doi.org/10.1186/s13227-023-00211-1 |
_version_ | 1785037491655409664 |
---|---|
author | Root, Zachary D. Jandzik, David Gould, Claire Allen, Cara Brewer, Margaux Medeiros, Daniel M. |
author_facet | Root, Zachary D. Jandzik, David Gould, Claire Allen, Cara Brewer, Margaux Medeiros, Daniel M. |
author_sort | Root, Zachary D. |
collection | PubMed |
description | The vertebrate head skeleton has evolved a myriad of forms since their divergence from invertebrate chordates. The connection between novel gene expression and cell types is therefore of importance in this process. The transformation of the jawed vertebrate (gnathostome) head skeleton from oral cirri to jointed jaw elements required a diversity of cartilages as well as changes in the patterning of these tissues. Although lampreys are a sister clade to gnathostomes, they display skeletal diversity with distinct gene expression and histologies, a useful model for addressing joint evolution. Specifically, the lamprey tissue known as mucocartilage has noted similarities with the jointed elements of the mandibular arch in jawed vertebrates. We thus asked whether the cells in lamprey mucocartilage and gnathostome joint tissue could be considered homologous. To do this, we characterized new genes that are involved in gnathostome joint formation and characterized the histochemical properties of lamprey skeletal types. We find that most of these genes are minimally found in mucocartilage and are likely later innovations, but we do identify new activity for gdf5/6/7b in both hyaline and mucocartilage, supporting its role as a chondrogenic regulator. Contrary to previous works, our histological assays do not find any perichondrial fibroblasts surrounding mucocartilage, suggesting that mucocartilage is non-skeletogenic tissue that is partially chondrified. Interestingly, we also identify new histochemical features of the lamprey otic capsule that diverge from normal hyaline. Paired with our new insights into lamprey mucocartilage, we propose a broader framework for skeletal evolution in which an ancestral soxD/E and gdf5/6/7 network directs mesenchyme along a spectrum of cartilage-like features. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13227-023-00211-1. |
format | Online Article Text |
id | pubmed-10161429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101614292023-05-06 Cartilage diversification and modularity drove the evolution of the ancestral vertebrate head skeleton Root, Zachary D. Jandzik, David Gould, Claire Allen, Cara Brewer, Margaux Medeiros, Daniel M. EvoDevo Research The vertebrate head skeleton has evolved a myriad of forms since their divergence from invertebrate chordates. The connection between novel gene expression and cell types is therefore of importance in this process. The transformation of the jawed vertebrate (gnathostome) head skeleton from oral cirri to jointed jaw elements required a diversity of cartilages as well as changes in the patterning of these tissues. Although lampreys are a sister clade to gnathostomes, they display skeletal diversity with distinct gene expression and histologies, a useful model for addressing joint evolution. Specifically, the lamprey tissue known as mucocartilage has noted similarities with the jointed elements of the mandibular arch in jawed vertebrates. We thus asked whether the cells in lamprey mucocartilage and gnathostome joint tissue could be considered homologous. To do this, we characterized new genes that are involved in gnathostome joint formation and characterized the histochemical properties of lamprey skeletal types. We find that most of these genes are minimally found in mucocartilage and are likely later innovations, but we do identify new activity for gdf5/6/7b in both hyaline and mucocartilage, supporting its role as a chondrogenic regulator. Contrary to previous works, our histological assays do not find any perichondrial fibroblasts surrounding mucocartilage, suggesting that mucocartilage is non-skeletogenic tissue that is partially chondrified. Interestingly, we also identify new histochemical features of the lamprey otic capsule that diverge from normal hyaline. Paired with our new insights into lamprey mucocartilage, we propose a broader framework for skeletal evolution in which an ancestral soxD/E and gdf5/6/7 network directs mesenchyme along a spectrum of cartilage-like features. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13227-023-00211-1. BioMed Central 2023-05-05 /pmc/articles/PMC10161429/ /pubmed/37147719 http://dx.doi.org/10.1186/s13227-023-00211-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Root, Zachary D. Jandzik, David Gould, Claire Allen, Cara Brewer, Margaux Medeiros, Daniel M. Cartilage diversification and modularity drove the evolution of the ancestral vertebrate head skeleton |
title | Cartilage diversification and modularity drove the evolution of the ancestral vertebrate head skeleton |
title_full | Cartilage diversification and modularity drove the evolution of the ancestral vertebrate head skeleton |
title_fullStr | Cartilage diversification and modularity drove the evolution of the ancestral vertebrate head skeleton |
title_full_unstemmed | Cartilage diversification and modularity drove the evolution of the ancestral vertebrate head skeleton |
title_short | Cartilage diversification and modularity drove the evolution of the ancestral vertebrate head skeleton |
title_sort | cartilage diversification and modularity drove the evolution of the ancestral vertebrate head skeleton |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161429/ https://www.ncbi.nlm.nih.gov/pubmed/37147719 http://dx.doi.org/10.1186/s13227-023-00211-1 |
work_keys_str_mv | AT rootzacharyd cartilagediversificationandmodularitydrovetheevolutionoftheancestralvertebrateheadskeleton AT jandzikdavid cartilagediversificationandmodularitydrovetheevolutionoftheancestralvertebrateheadskeleton AT gouldclaire cartilagediversificationandmodularitydrovetheevolutionoftheancestralvertebrateheadskeleton AT allencara cartilagediversificationandmodularitydrovetheevolutionoftheancestralvertebrateheadskeleton AT brewermargaux cartilagediversificationandmodularitydrovetheevolutionoftheancestralvertebrateheadskeleton AT medeirosdanielm cartilagediversificationandmodularitydrovetheevolutionoftheancestralvertebrateheadskeleton |