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Chronology of embryonic and gonadal development in the Reeves’ turtle, Mauremys reevesii
Temperature-dependent sex determination (TSD) is a mechanism in which environmental temperature, rather than innate zygotic genotype, determines the fate of sexual differentiation during embryonic development. Reeves’ turtle (also known as the Chinese three-keeled pond turtle, Mauremys reevesii) exh...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270433/ https://www.ncbi.nlm.nih.gov/pubmed/35804180 http://dx.doi.org/10.1038/s41598-022-15515-w |
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author | Akashi, Hiroshi Kubota, Manami Yamamoto, Hibiki Miyaoku, Kaori Yamagishi, Genki Miyagawa, Shinichi |
author_facet | Akashi, Hiroshi Kubota, Manami Yamamoto, Hibiki Miyaoku, Kaori Yamagishi, Genki Miyagawa, Shinichi |
author_sort | Akashi, Hiroshi |
collection | PubMed |
description | Temperature-dependent sex determination (TSD) is a mechanism in which environmental temperature, rather than innate zygotic genotype, determines the fate of sexual differentiation during embryonic development. Reeves’ turtle (also known as the Chinese three-keeled pond turtle, Mauremys reevesii) exhibits TSD and is the only species whose genome has been determined in Geoemydidae to date. Thus, M. reevesii occupy phylogenetically important position for the study of TSD and can be compared to other TSD species to elucidate the underlying molecular mechanism of this process. Nevertheless, neither embryogenesis nor gonadogenesis has been described in this species. Therefore, herein, we investigated the chronology of normal embryonic development and gonadal structures in M. reevesii under both female- and male-producing incubation temperatures (FPT 31 °C or MPT 26 °C, respectively). External morphology remains indistinct between the two temperature regimes throughout the studied embryonic stages. However, the gonadal ridges present on the mesonephros at stage 16 develop and sexually differentiate at FPT and MPT. Ovarian and testicular structures begin to develop at stages 18–19 at FPT and stages 20–21 at MPT, respectively, and thus, the sexual differentiation of gonadal structures began earlier in the embryos at FPT than at MPT. Our results suggest that temperature sensitive period, at which the gonadal structures remain sexually undifferentiated, spans from stage 16 (or earlier) to stages 18–19 at FPT and to stages 20–21 at MPT. Understanding the temperature-dependent differentiation in gonadal structures during embryonic development is a prerequisite for investigating molecular basis underlying TSD. Thus, the result of the present study will facilitate further developmental studies on TSD in M. reevesii. |
format | Online Article Text |
id | pubmed-9270433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92704332022-07-10 Chronology of embryonic and gonadal development in the Reeves’ turtle, Mauremys reevesii Akashi, Hiroshi Kubota, Manami Yamamoto, Hibiki Miyaoku, Kaori Yamagishi, Genki Miyagawa, Shinichi Sci Rep Article Temperature-dependent sex determination (TSD) is a mechanism in which environmental temperature, rather than innate zygotic genotype, determines the fate of sexual differentiation during embryonic development. Reeves’ turtle (also known as the Chinese three-keeled pond turtle, Mauremys reevesii) exhibits TSD and is the only species whose genome has been determined in Geoemydidae to date. Thus, M. reevesii occupy phylogenetically important position for the study of TSD and can be compared to other TSD species to elucidate the underlying molecular mechanism of this process. Nevertheless, neither embryogenesis nor gonadogenesis has been described in this species. Therefore, herein, we investigated the chronology of normal embryonic development and gonadal structures in M. reevesii under both female- and male-producing incubation temperatures (FPT 31 °C or MPT 26 °C, respectively). External morphology remains indistinct between the two temperature regimes throughout the studied embryonic stages. However, the gonadal ridges present on the mesonephros at stage 16 develop and sexually differentiate at FPT and MPT. Ovarian and testicular structures begin to develop at stages 18–19 at FPT and stages 20–21 at MPT, respectively, and thus, the sexual differentiation of gonadal structures began earlier in the embryos at FPT than at MPT. Our results suggest that temperature sensitive period, at which the gonadal structures remain sexually undifferentiated, spans from stage 16 (or earlier) to stages 18–19 at FPT and to stages 20–21 at MPT. Understanding the temperature-dependent differentiation in gonadal structures during embryonic development is a prerequisite for investigating molecular basis underlying TSD. Thus, the result of the present study will facilitate further developmental studies on TSD in M. reevesii. Nature Publishing Group UK 2022-07-08 /pmc/articles/PMC9270433/ /pubmed/35804180 http://dx.doi.org/10.1038/s41598-022-15515-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 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/) . |
spellingShingle | Article Akashi, Hiroshi Kubota, Manami Yamamoto, Hibiki Miyaoku, Kaori Yamagishi, Genki Miyagawa, Shinichi Chronology of embryonic and gonadal development in the Reeves’ turtle, Mauremys reevesii |
title | Chronology of embryonic and gonadal development in the Reeves’ turtle, Mauremys reevesii |
title_full | Chronology of embryonic and gonadal development in the Reeves’ turtle, Mauremys reevesii |
title_fullStr | Chronology of embryonic and gonadal development in the Reeves’ turtle, Mauremys reevesii |
title_full_unstemmed | Chronology of embryonic and gonadal development in the Reeves’ turtle, Mauremys reevesii |
title_short | Chronology of embryonic and gonadal development in the Reeves’ turtle, Mauremys reevesii |
title_sort | chronology of embryonic and gonadal development in the reeves’ turtle, mauremys reevesii |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270433/ https://www.ncbi.nlm.nih.gov/pubmed/35804180 http://dx.doi.org/10.1038/s41598-022-15515-w |
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