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Maternal GABAergic and GnRH/corazonin pathway modulates egg diapause phenotype of the silkworm Bombyx mori
Diapause represents a major developmental switch in insects and is a seasonal adaptation that evolved as a specific subtype of dormancy in most insect species to ensure survival under unfavorable environmental conditions and synchronize populations. However, the hierarchical relationship of the mole...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817158/ https://www.ncbi.nlm.nih.gov/pubmed/33443213 http://dx.doi.org/10.1073/pnas.2020028118 |
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author | Tsuchiya, Ryoma Kaneshima, Aino Kobayashi, Masakazu Yamazaki, Maki Takasu, Yoko Sezutsu, Hideki Tanaka, Yoshiaki Mizoguchi, Akira Shiomi, Kunihiro |
author_facet | Tsuchiya, Ryoma Kaneshima, Aino Kobayashi, Masakazu Yamazaki, Maki Takasu, Yoko Sezutsu, Hideki Tanaka, Yoshiaki Mizoguchi, Akira Shiomi, Kunihiro |
author_sort | Tsuchiya, Ryoma |
collection | PubMed |
description | Diapause represents a major developmental switch in insects and is a seasonal adaptation that evolved as a specific subtype of dormancy in most insect species to ensure survival under unfavorable environmental conditions and synchronize populations. However, the hierarchical relationship of the molecular mechanisms involved in the perception of environmental signals to integration in morphological, physiological, behavioral, and reproductive responses remains unclear. In the bivoltine strain of the silkworm Bombyx mori, embryonic diapause is induced transgenerationally as a maternal effect. Progeny diapause is determined by the environmental temperature during embryonic development of the mother. Here, we show that the hierarchical pathway consists of a γ-aminobutyric acid (GABA)ergic and corazonin signaling system modulating progeny diapause induction via diapause hormone release, which may be finely tuned by the temperature-dependent expression of plasma membrane GABA transporter. Furthermore, this signaling pathway possesses similar features to the gonadotropin-releasing hormone (GnRH) signaling system for seasonal reproductive plasticity in vertebrates. |
format | Online Article Text |
id | pubmed-7817158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-78171582021-01-28 Maternal GABAergic and GnRH/corazonin pathway modulates egg diapause phenotype of the silkworm Bombyx mori Tsuchiya, Ryoma Kaneshima, Aino Kobayashi, Masakazu Yamazaki, Maki Takasu, Yoko Sezutsu, Hideki Tanaka, Yoshiaki Mizoguchi, Akira Shiomi, Kunihiro Proc Natl Acad Sci U S A Biological Sciences Diapause represents a major developmental switch in insects and is a seasonal adaptation that evolved as a specific subtype of dormancy in most insect species to ensure survival under unfavorable environmental conditions and synchronize populations. However, the hierarchical relationship of the molecular mechanisms involved in the perception of environmental signals to integration in morphological, physiological, behavioral, and reproductive responses remains unclear. In the bivoltine strain of the silkworm Bombyx mori, embryonic diapause is induced transgenerationally as a maternal effect. Progeny diapause is determined by the environmental temperature during embryonic development of the mother. Here, we show that the hierarchical pathway consists of a γ-aminobutyric acid (GABA)ergic and corazonin signaling system modulating progeny diapause induction via diapause hormone release, which may be finely tuned by the temperature-dependent expression of plasma membrane GABA transporter. Furthermore, this signaling pathway possesses similar features to the gonadotropin-releasing hormone (GnRH) signaling system for seasonal reproductive plasticity in vertebrates. National Academy of Sciences 2021-01-05 2020-12-28 /pmc/articles/PMC7817158/ /pubmed/33443213 http://dx.doi.org/10.1073/pnas.2020028118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Tsuchiya, Ryoma Kaneshima, Aino Kobayashi, Masakazu Yamazaki, Maki Takasu, Yoko Sezutsu, Hideki Tanaka, Yoshiaki Mizoguchi, Akira Shiomi, Kunihiro Maternal GABAergic and GnRH/corazonin pathway modulates egg diapause phenotype of the silkworm Bombyx mori |
title | Maternal GABAergic and GnRH/corazonin pathway modulates egg diapause phenotype of the silkworm Bombyx mori |
title_full | Maternal GABAergic and GnRH/corazonin pathway modulates egg diapause phenotype of the silkworm Bombyx mori |
title_fullStr | Maternal GABAergic and GnRH/corazonin pathway modulates egg diapause phenotype of the silkworm Bombyx mori |
title_full_unstemmed | Maternal GABAergic and GnRH/corazonin pathway modulates egg diapause phenotype of the silkworm Bombyx mori |
title_short | Maternal GABAergic and GnRH/corazonin pathway modulates egg diapause phenotype of the silkworm Bombyx mori |
title_sort | maternal gabaergic and gnrh/corazonin pathway modulates egg diapause phenotype of the silkworm bombyx mori |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817158/ https://www.ncbi.nlm.nih.gov/pubmed/33443213 http://dx.doi.org/10.1073/pnas.2020028118 |
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