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Ecdysone promotes growth of imaginal discs through the regulation of Thor in D. melanogaster
Animals have a determined species-specific body size that results from the combined action of hormones and signaling pathways regulating growth rate and duration. In Drosophila, the steroid hormone ecdysone controls developmental transitions, thereby regulating the duration of the growth period. Her...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510524/ https://www.ncbi.nlm.nih.gov/pubmed/26198204 http://dx.doi.org/10.1038/srep12383 |
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author | Herboso, Leire Oliveira, Marisa M. Talamillo, Ana Pérez, Coralia González, Monika Martín, David Sutherland, James D. Shingleton, Alexander W. Mirth, Christen K. Barrio, Rosa |
author_facet | Herboso, Leire Oliveira, Marisa M. Talamillo, Ana Pérez, Coralia González, Monika Martín, David Sutherland, James D. Shingleton, Alexander W. Mirth, Christen K. Barrio, Rosa |
author_sort | Herboso, Leire |
collection | PubMed |
description | Animals have a determined species-specific body size that results from the combined action of hormones and signaling pathways regulating growth rate and duration. In Drosophila, the steroid hormone ecdysone controls developmental transitions, thereby regulating the duration of the growth period. Here we show that ecdysone promotes the growth of imaginal discs in mid-third instar larvae, since imaginal discs from larvae with reduced or no ecdysone synthesis are smaller than wild type due to smaller and fewer cells. We show that insulin-like peptides are produced and secreted normally in larvae with reduced ecdysone synthesis, and upstream components of insulin/insulin-like signaling are activated in their discs. Instead, ecdysone appears to regulate the growth of imaginal discs via Thor/4E-BP, a negative growth regulator downstream of the insulin/insulin-like growth factor/Tor pathways. Discs from larvae with reduced ecdysone synthesis have elevated levels of Thor, while mutations in Thor partially rescue their growth. The regulation of organ growth by ecdysone is evolutionarily conserved in hemimetabolous insects, as shown by our results obtained using Blattella germanica. In summary, our data provide new insights into the relationship between components of the insulin/insulin-like/Tor and ecdysone pathways in the control of organ growth. |
format | Online Article Text |
id | pubmed-4510524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45105242015-07-28 Ecdysone promotes growth of imaginal discs through the regulation of Thor in D. melanogaster Herboso, Leire Oliveira, Marisa M. Talamillo, Ana Pérez, Coralia González, Monika Martín, David Sutherland, James D. Shingleton, Alexander W. Mirth, Christen K. Barrio, Rosa Sci Rep Article Animals have a determined species-specific body size that results from the combined action of hormones and signaling pathways regulating growth rate and duration. In Drosophila, the steroid hormone ecdysone controls developmental transitions, thereby regulating the duration of the growth period. Here we show that ecdysone promotes the growth of imaginal discs in mid-third instar larvae, since imaginal discs from larvae with reduced or no ecdysone synthesis are smaller than wild type due to smaller and fewer cells. We show that insulin-like peptides are produced and secreted normally in larvae with reduced ecdysone synthesis, and upstream components of insulin/insulin-like signaling are activated in their discs. Instead, ecdysone appears to regulate the growth of imaginal discs via Thor/4E-BP, a negative growth regulator downstream of the insulin/insulin-like growth factor/Tor pathways. Discs from larvae with reduced ecdysone synthesis have elevated levels of Thor, while mutations in Thor partially rescue their growth. The regulation of organ growth by ecdysone is evolutionarily conserved in hemimetabolous insects, as shown by our results obtained using Blattella germanica. In summary, our data provide new insights into the relationship between components of the insulin/insulin-like/Tor and ecdysone pathways in the control of organ growth. Nature Publishing Group 2015-07-22 /pmc/articles/PMC4510524/ /pubmed/26198204 http://dx.doi.org/10.1038/srep12383 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Herboso, Leire Oliveira, Marisa M. Talamillo, Ana Pérez, Coralia González, Monika Martín, David Sutherland, James D. Shingleton, Alexander W. Mirth, Christen K. Barrio, Rosa Ecdysone promotes growth of imaginal discs through the regulation of Thor in D. melanogaster |
title | Ecdysone promotes growth of imaginal discs through the regulation of Thor in D. melanogaster |
title_full | Ecdysone promotes growth of imaginal discs through the regulation of Thor in D. melanogaster |
title_fullStr | Ecdysone promotes growth of imaginal discs through the regulation of Thor in D. melanogaster |
title_full_unstemmed | Ecdysone promotes growth of imaginal discs through the regulation of Thor in D. melanogaster |
title_short | Ecdysone promotes growth of imaginal discs through the regulation of Thor in D. melanogaster |
title_sort | ecdysone promotes growth of imaginal discs through the regulation of thor in d. melanogaster |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510524/ https://www.ncbi.nlm.nih.gov/pubmed/26198204 http://dx.doi.org/10.1038/srep12383 |
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