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Deep time perspective on turtle neck evolution: chasing the Hox code by vertebral morphology
The unparalleled ability of turtle neck retraction is possible in three different modes, which characterize stem turtles, living side-necked (Pleurodira), and hidden-necked (Cryptodira) turtles, respectively. Despite the conservatism in vertebral count among turtles, there is significant functional...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566328/ https://www.ncbi.nlm.nih.gov/pubmed/28827543 http://dx.doi.org/10.1038/s41598-017-09133-0 |
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author | Böhmer, Christine Werneburg, Ingmar |
author_facet | Böhmer, Christine Werneburg, Ingmar |
author_sort | Böhmer, Christine |
collection | PubMed |
description | The unparalleled ability of turtle neck retraction is possible in three different modes, which characterize stem turtles, living side-necked (Pleurodira), and hidden-necked (Cryptodira) turtles, respectively. Despite the conservatism in vertebral count among turtles, there is significant functional and morphological regionalization in the cervical vertebral column. Since Hox genes play a fundamental role in determining the differentiation in vertebra morphology and based on our reconstruction of evolutionary genetics in deep time, we hypothesize genetic differences among the turtle groups and between turtles and other land vertebrates. We correlated anterior Hox gene expression and the quantifiable shape of the vertebrae to investigate the morphological modularity in the neck across living and extinct turtles. This permitted the reconstruction of the hypothetical ancestral Hox code pattern of the whole turtle clade. The scenario of the evolution of axial patterning in turtles indicates shifts in the spatial expression of HoxA-5 in relation to the reduction of cervical ribs in modern turtles and of HoxB-5 linked with a lower morphological differentiation between the anterior cervical vertebrae observed in cryptodirans. By comparison with the mammalian pattern, we illustrate how the fixed count of eight cervical vertebrae in turtles resulted from the emergence of the unique turtle shell. |
format | Online Article Text |
id | pubmed-5566328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55663282017-08-23 Deep time perspective on turtle neck evolution: chasing the Hox code by vertebral morphology Böhmer, Christine Werneburg, Ingmar Sci Rep Article The unparalleled ability of turtle neck retraction is possible in three different modes, which characterize stem turtles, living side-necked (Pleurodira), and hidden-necked (Cryptodira) turtles, respectively. Despite the conservatism in vertebral count among turtles, there is significant functional and morphological regionalization in the cervical vertebral column. Since Hox genes play a fundamental role in determining the differentiation in vertebra morphology and based on our reconstruction of evolutionary genetics in deep time, we hypothesize genetic differences among the turtle groups and between turtles and other land vertebrates. We correlated anterior Hox gene expression and the quantifiable shape of the vertebrae to investigate the morphological modularity in the neck across living and extinct turtles. This permitted the reconstruction of the hypothetical ancestral Hox code pattern of the whole turtle clade. The scenario of the evolution of axial patterning in turtles indicates shifts in the spatial expression of HoxA-5 in relation to the reduction of cervical ribs in modern turtles and of HoxB-5 linked with a lower morphological differentiation between the anterior cervical vertebrae observed in cryptodirans. By comparison with the mammalian pattern, we illustrate how the fixed count of eight cervical vertebrae in turtles resulted from the emergence of the unique turtle shell. Nature Publishing Group UK 2017-08-21 /pmc/articles/PMC5566328/ /pubmed/28827543 http://dx.doi.org/10.1038/s41598-017-09133-0 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Böhmer, Christine Werneburg, Ingmar Deep time perspective on turtle neck evolution: chasing the Hox code by vertebral morphology |
title | Deep time perspective on turtle neck evolution: chasing the Hox code by vertebral morphology |
title_full | Deep time perspective on turtle neck evolution: chasing the Hox code by vertebral morphology |
title_fullStr | Deep time perspective on turtle neck evolution: chasing the Hox code by vertebral morphology |
title_full_unstemmed | Deep time perspective on turtle neck evolution: chasing the Hox code by vertebral morphology |
title_short | Deep time perspective on turtle neck evolution: chasing the Hox code by vertebral morphology |
title_sort | deep time perspective on turtle neck evolution: chasing the hox code by vertebral morphology |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566328/ https://www.ncbi.nlm.nih.gov/pubmed/28827543 http://dx.doi.org/10.1038/s41598-017-09133-0 |
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