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The insect somatostatin pathway gates vitellogenesis progression during reproductive maturation and the post-mating response
Vitellogenesis (yolk accumulation) begins upon eclosion and continues through the process of sexual maturation. Upon reaching sexual maturity, vitellogenesis is placed on hold until it is induced again by mating. However, the mechanisms that gate vitellogenesis in response to developmental and repro...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857180/ https://www.ncbi.nlm.nih.gov/pubmed/35181671 http://dx.doi.org/10.1038/s41467-022-28592-2 |
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author | Zhang, Chen Kim, Anmo J. Rivera-Perez, Crisalesandra Noriega, Fernando G. Kim, Young-Joon |
author_facet | Zhang, Chen Kim, Anmo J. Rivera-Perez, Crisalesandra Noriega, Fernando G. Kim, Young-Joon |
author_sort | Zhang, Chen |
collection | PubMed |
description | Vitellogenesis (yolk accumulation) begins upon eclosion and continues through the process of sexual maturation. Upon reaching sexual maturity, vitellogenesis is placed on hold until it is induced again by mating. However, the mechanisms that gate vitellogenesis in response to developmental and reproductive signals remain unclear. Here, we have identified the neuropeptide allatostatin-C (AstC)-producing neurons that gate both the initiation of vitellogenesis that occurs post-eclosion and its re-initiation post-mating. During sexual maturation, the AstC neurons receive excitatory inputs from Sex Peptide Abdominal Ganglion (SAG) neurons. In mature virgin females, high sustained activity of SAG neurons shuts off vitellogenesis via continuous activation of the AstC neurons. Upon mating, however, Sex Peptide inhibits SAG neurons, leading to deactivation of the AstC neurons. As a result, this permits both JH biosynthesis and the progression of vitellogenesis in mated females. Our work has uncovered a central neural circuit that gates the progression of oogenesis. |
format | Online Article Text |
id | pubmed-8857180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88571802022-03-04 The insect somatostatin pathway gates vitellogenesis progression during reproductive maturation and the post-mating response Zhang, Chen Kim, Anmo J. Rivera-Perez, Crisalesandra Noriega, Fernando G. Kim, Young-Joon Nat Commun Article Vitellogenesis (yolk accumulation) begins upon eclosion and continues through the process of sexual maturation. Upon reaching sexual maturity, vitellogenesis is placed on hold until it is induced again by mating. However, the mechanisms that gate vitellogenesis in response to developmental and reproductive signals remain unclear. Here, we have identified the neuropeptide allatostatin-C (AstC)-producing neurons that gate both the initiation of vitellogenesis that occurs post-eclosion and its re-initiation post-mating. During sexual maturation, the AstC neurons receive excitatory inputs from Sex Peptide Abdominal Ganglion (SAG) neurons. In mature virgin females, high sustained activity of SAG neurons shuts off vitellogenesis via continuous activation of the AstC neurons. Upon mating, however, Sex Peptide inhibits SAG neurons, leading to deactivation of the AstC neurons. As a result, this permits both JH biosynthesis and the progression of vitellogenesis in mated females. Our work has uncovered a central neural circuit that gates the progression of oogenesis. Nature Publishing Group UK 2022-02-18 /pmc/articles/PMC8857180/ /pubmed/35181671 http://dx.doi.org/10.1038/s41467-022-28592-2 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhang, Chen Kim, Anmo J. Rivera-Perez, Crisalesandra Noriega, Fernando G. Kim, Young-Joon The insect somatostatin pathway gates vitellogenesis progression during reproductive maturation and the post-mating response |
title | The insect somatostatin pathway gates vitellogenesis progression during reproductive maturation and the post-mating response |
title_full | The insect somatostatin pathway gates vitellogenesis progression during reproductive maturation and the post-mating response |
title_fullStr | The insect somatostatin pathway gates vitellogenesis progression during reproductive maturation and the post-mating response |
title_full_unstemmed | The insect somatostatin pathway gates vitellogenesis progression during reproductive maturation and the post-mating response |
title_short | The insect somatostatin pathway gates vitellogenesis progression during reproductive maturation and the post-mating response |
title_sort | insect somatostatin pathway gates vitellogenesis progression during reproductive maturation and the post-mating response |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857180/ https://www.ncbi.nlm.nih.gov/pubmed/35181671 http://dx.doi.org/10.1038/s41467-022-28592-2 |
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