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Turtle skull development unveils a molecular basis for amniote cranial diversity
Amniote skulls display diverse architectural patterns including remarkable variations in the number of temporal arches surrounding the upper and lower temporal fenestrae. However, the cellular and molecular basis underlying this diversification remains elusive. Turtles are a useful model to understa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651123/ https://www.ncbi.nlm.nih.gov/pubmed/37967181 http://dx.doi.org/10.1126/sciadv.adi6765 |
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author | Sato, Hiromu Adachi, Noritaka Kondo, Satomi Kitayama, Chiyo Tokita, Masayoshi |
author_facet | Sato, Hiromu Adachi, Noritaka Kondo, Satomi Kitayama, Chiyo Tokita, Masayoshi |
author_sort | Sato, Hiromu |
collection | PubMed |
description | Amniote skulls display diverse architectural patterns including remarkable variations in the number of temporal arches surrounding the upper and lower temporal fenestrae. However, the cellular and molecular basis underlying this diversification remains elusive. Turtles are a useful model to understand skull diversity due to the presence of secondarily closed temporal fenestrae and different extents of temporal emarginations (marginal reduction of dermal bones). Here, we analyzed embryos of three turtle species with varying degrees of temporal emargination and identified shared widespread coexpression of upstream osteogenic genes Msx2 and Runx2 and species-specific expression of more downstream osteogenic genes Sp7 and Sparc in the head. Further analysis of representative amniote embryos revealed differential expression patterns of osteogenic genes in the temporal region, suggesting that the spatiotemporal regulation of Msx2, Runx2, and Sp7 distinguishes the temporal skull morphology among amniotes. Moreover, the presence of Msx2- and/or Runx2-positive temporal mesenchyme with osteogenic potential may have contributed to their extremely diverse cranial morphology in reptiles. |
format | Online Article Text |
id | pubmed-10651123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-106511232023-11-15 Turtle skull development unveils a molecular basis for amniote cranial diversity Sato, Hiromu Adachi, Noritaka Kondo, Satomi Kitayama, Chiyo Tokita, Masayoshi Sci Adv Earth, Environmental, Ecological, and Space Sciences Amniote skulls display diverse architectural patterns including remarkable variations in the number of temporal arches surrounding the upper and lower temporal fenestrae. However, the cellular and molecular basis underlying this diversification remains elusive. Turtles are a useful model to understand skull diversity due to the presence of secondarily closed temporal fenestrae and different extents of temporal emarginations (marginal reduction of dermal bones). Here, we analyzed embryos of three turtle species with varying degrees of temporal emargination and identified shared widespread coexpression of upstream osteogenic genes Msx2 and Runx2 and species-specific expression of more downstream osteogenic genes Sp7 and Sparc in the head. Further analysis of representative amniote embryos revealed differential expression patterns of osteogenic genes in the temporal region, suggesting that the spatiotemporal regulation of Msx2, Runx2, and Sp7 distinguishes the temporal skull morphology among amniotes. Moreover, the presence of Msx2- and/or Runx2-positive temporal mesenchyme with osteogenic potential may have contributed to their extremely diverse cranial morphology in reptiles. American Association for the Advancement of Science 2023-11-15 /pmc/articles/PMC10651123/ /pubmed/37967181 http://dx.doi.org/10.1126/sciadv.adi6765 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Earth, Environmental, Ecological, and Space Sciences Sato, Hiromu Adachi, Noritaka Kondo, Satomi Kitayama, Chiyo Tokita, Masayoshi Turtle skull development unveils a molecular basis for amniote cranial diversity |
title | Turtle skull development unveils a molecular basis for amniote cranial diversity |
title_full | Turtle skull development unveils a molecular basis for amniote cranial diversity |
title_fullStr | Turtle skull development unveils a molecular basis for amniote cranial diversity |
title_full_unstemmed | Turtle skull development unveils a molecular basis for amniote cranial diversity |
title_short | Turtle skull development unveils a molecular basis for amniote cranial diversity |
title_sort | turtle skull development unveils a molecular basis for amniote cranial diversity |
topic | Earth, Environmental, Ecological, and Space Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651123/ https://www.ncbi.nlm.nih.gov/pubmed/37967181 http://dx.doi.org/10.1126/sciadv.adi6765 |
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