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Embryonic lethality is not sufficient to explain hourglass-like conservation of vertebrate embryos

BACKGROUND: Understanding the general trends in developmental changes during animal evolution, which are often associated with morphological diversification, has long been a central issue in evolutionary developmental biology. Recent comparative transcriptomic studies revealed that gene expression p...

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Autores principales: Uchida, Yui, Uesaka, Masahiro, Yamamoto, Takayoshi, Takeda, Hiroyuki, Irie, Naoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855935/
https://www.ncbi.nlm.nih.gov/pubmed/29568479
http://dx.doi.org/10.1186/s13227-018-0095-0
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author Uchida, Yui
Uesaka, Masahiro
Yamamoto, Takayoshi
Takeda, Hiroyuki
Irie, Naoki
author_facet Uchida, Yui
Uesaka, Masahiro
Yamamoto, Takayoshi
Takeda, Hiroyuki
Irie, Naoki
author_sort Uchida, Yui
collection PubMed
description BACKGROUND: Understanding the general trends in developmental changes during animal evolution, which are often associated with morphological diversification, has long been a central issue in evolutionary developmental biology. Recent comparative transcriptomic studies revealed that gene expression profiles of mid-embryonic period tend to be more evolutionarily conserved than those in earlier or later periods. While the hourglass-like divergence of developmental processes has been demonstrated in a variety of animal groups such as vertebrates, arthropods, and nematodes, the exact mechanism leading to this mid-embryonic conservation remains to be clarified. One possibility is that the mid-embryonic period (pharyngula period in vertebrates) is highly prone to embryonic lethality, and the resulting negative selections lead to evolutionary conservation of this phase. Here, we tested this “mid-embryonic lethality hypothesis” by measuring the rate of lethal phenotypes of three different species of vertebrate embryos subjected to two kinds of perturbations: transient perturbations and genetic mutations. RESULTS: By subjecting zebrafish (Danio rerio), African clawed frog (Xenopus laevis), and chicken (Gallus gallus) embryos to transient perturbations, namely heat shock and inhibitor treatments during three developmental periods [early (represented by blastula and gastrula), pharyngula, and late], we found that the early stages showed the highest rate of lethal phenotypes in all three species. This result was corroborated by perturbation with genetic mutations. By tracking the survival rate of wild-type embryos and embryos with genetic mutations induced by UV irradiation in zebrafish and African clawed frogs, we found that the highest decrease in survival rate was at the early stages particularly around gastrulation in both these species. CONCLUSION: In opposition to the “mid-embryonic lethality hypothesis,” our results consistently showed that the stage with the highest lethality was not around the conserved pharyngula period, but rather around the early period in all the vertebrate species tested. These results suggest that negative selection by embryonic lethality could not explain hourglass-like conservation of animal embryos. This highlights the potential contribution of alternative mechanisms such as the diversifying effect of positive selections against earlier and later stages, and developmental constraints which lead to conservation of mid-embryonic stages. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13227-018-0095-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-58559352018-03-22 Embryonic lethality is not sufficient to explain hourglass-like conservation of vertebrate embryos Uchida, Yui Uesaka, Masahiro Yamamoto, Takayoshi Takeda, Hiroyuki Irie, Naoki EvoDevo Research BACKGROUND: Understanding the general trends in developmental changes during animal evolution, which are often associated with morphological diversification, has long been a central issue in evolutionary developmental biology. Recent comparative transcriptomic studies revealed that gene expression profiles of mid-embryonic period tend to be more evolutionarily conserved than those in earlier or later periods. While the hourglass-like divergence of developmental processes has been demonstrated in a variety of animal groups such as vertebrates, arthropods, and nematodes, the exact mechanism leading to this mid-embryonic conservation remains to be clarified. One possibility is that the mid-embryonic period (pharyngula period in vertebrates) is highly prone to embryonic lethality, and the resulting negative selections lead to evolutionary conservation of this phase. Here, we tested this “mid-embryonic lethality hypothesis” by measuring the rate of lethal phenotypes of three different species of vertebrate embryos subjected to two kinds of perturbations: transient perturbations and genetic mutations. RESULTS: By subjecting zebrafish (Danio rerio), African clawed frog (Xenopus laevis), and chicken (Gallus gallus) embryos to transient perturbations, namely heat shock and inhibitor treatments during three developmental periods [early (represented by blastula and gastrula), pharyngula, and late], we found that the early stages showed the highest rate of lethal phenotypes in all three species. This result was corroborated by perturbation with genetic mutations. By tracking the survival rate of wild-type embryos and embryos with genetic mutations induced by UV irradiation in zebrafish and African clawed frogs, we found that the highest decrease in survival rate was at the early stages particularly around gastrulation in both these species. CONCLUSION: In opposition to the “mid-embryonic lethality hypothesis,” our results consistently showed that the stage with the highest lethality was not around the conserved pharyngula period, but rather around the early period in all the vertebrate species tested. These results suggest that negative selection by embryonic lethality could not explain hourglass-like conservation of animal embryos. This highlights the potential contribution of alternative mechanisms such as the diversifying effect of positive selections against earlier and later stages, and developmental constraints which lead to conservation of mid-embryonic stages. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13227-018-0095-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-16 /pmc/articles/PMC5855935/ /pubmed/29568479 http://dx.doi.org/10.1186/s13227-018-0095-0 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Uchida, Yui
Uesaka, Masahiro
Yamamoto, Takayoshi
Takeda, Hiroyuki
Irie, Naoki
Embryonic lethality is not sufficient to explain hourglass-like conservation of vertebrate embryos
title Embryonic lethality is not sufficient to explain hourglass-like conservation of vertebrate embryos
title_full Embryonic lethality is not sufficient to explain hourglass-like conservation of vertebrate embryos
title_fullStr Embryonic lethality is not sufficient to explain hourglass-like conservation of vertebrate embryos
title_full_unstemmed Embryonic lethality is not sufficient to explain hourglass-like conservation of vertebrate embryos
title_short Embryonic lethality is not sufficient to explain hourglass-like conservation of vertebrate embryos
title_sort embryonic lethality is not sufficient to explain hourglass-like conservation of vertebrate embryos
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855935/
https://www.ncbi.nlm.nih.gov/pubmed/29568479
http://dx.doi.org/10.1186/s13227-018-0095-0
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