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The tanning hormone, bursicon, does not act directly on the epidermis to tan the Drosophila exoskeleton

BACKGROUND: In insects, continuous growth requires the periodic replacement of the exoskeleton. Once the remains of the exoskeleton from the previous stage have been shed during ecdysis, the new one is rapidly sclerotized (hardened) and melanized (pigmented), a process collectively known as tanning....

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Autores principales: Flaven-Pouchon, Justin, Alvarez, Javier V., Rojas, Candy, Ewer, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029472/
https://www.ncbi.nlm.nih.gov/pubmed/32075655
http://dx.doi.org/10.1186/s12915-020-0742-5
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author Flaven-Pouchon, Justin
Alvarez, Javier V.
Rojas, Candy
Ewer, John
author_facet Flaven-Pouchon, Justin
Alvarez, Javier V.
Rojas, Candy
Ewer, John
author_sort Flaven-Pouchon, Justin
collection PubMed
description BACKGROUND: In insects, continuous growth requires the periodic replacement of the exoskeleton. Once the remains of the exoskeleton from the previous stage have been shed during ecdysis, the new one is rapidly sclerotized (hardened) and melanized (pigmented), a process collectively known as tanning. The rapid tanning that occurs after ecdysis is critical for insect survival, as it reduces desiccation, and gives the exoskeleton the rigidity needed to support the internal organs and to provide a solid anchor for the muscles. This rapid postecdysial tanning is triggered by the “tanning hormone”, bursicon. Since bursicon is released into the hemolymph, it has naturally been assumed that it would act on the epidermal cells to cause the tanning of the overlying exoskeleton. RESULTS: Here we investigated the site of bursicon action in Drosophila by examining the consequences on tanning of disabling the bursicon receptor (encoded by the rickets gene) in different tissues. To our surprise, we found that rapid tanning does not require rickets function in the epidermis but requires it instead in peptidergic neurons of the ventral nervous system (VNS). Although we were unable to identify the signal that is transmitted from the VNS to the epidermis, we show that neurons that express the Drosophila insulin-like peptide ILP7, but not the ILP7 peptide itself, are involved. In addition, we found that some of the bursicon targets involved in melanization are different from those that cause sclerotization. CONCLUSIONS: Our findings show that bursicon does not act directly on the epidermis to cause the tanning of the overlying exoskeleton but instead requires an intermediary messenger produced by peptidergic neurons within the central nervous system. Thus, this work has uncovered an unexpected layer of control in a process that is critical for insect survival, which will significantly alter the direction of future research aimed at understanding how rapid postecdysial tanning occurs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-020-0742-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-70294722020-02-25 The tanning hormone, bursicon, does not act directly on the epidermis to tan the Drosophila exoskeleton Flaven-Pouchon, Justin Alvarez, Javier V. Rojas, Candy Ewer, John BMC Biol Research Article BACKGROUND: In insects, continuous growth requires the periodic replacement of the exoskeleton. Once the remains of the exoskeleton from the previous stage have been shed during ecdysis, the new one is rapidly sclerotized (hardened) and melanized (pigmented), a process collectively known as tanning. The rapid tanning that occurs after ecdysis is critical for insect survival, as it reduces desiccation, and gives the exoskeleton the rigidity needed to support the internal organs and to provide a solid anchor for the muscles. This rapid postecdysial tanning is triggered by the “tanning hormone”, bursicon. Since bursicon is released into the hemolymph, it has naturally been assumed that it would act on the epidermal cells to cause the tanning of the overlying exoskeleton. RESULTS: Here we investigated the site of bursicon action in Drosophila by examining the consequences on tanning of disabling the bursicon receptor (encoded by the rickets gene) in different tissues. To our surprise, we found that rapid tanning does not require rickets function in the epidermis but requires it instead in peptidergic neurons of the ventral nervous system (VNS). Although we were unable to identify the signal that is transmitted from the VNS to the epidermis, we show that neurons that express the Drosophila insulin-like peptide ILP7, but not the ILP7 peptide itself, are involved. In addition, we found that some of the bursicon targets involved in melanization are different from those that cause sclerotization. CONCLUSIONS: Our findings show that bursicon does not act directly on the epidermis to cause the tanning of the overlying exoskeleton but instead requires an intermediary messenger produced by peptidergic neurons within the central nervous system. Thus, this work has uncovered an unexpected layer of control in a process that is critical for insect survival, which will significantly alter the direction of future research aimed at understanding how rapid postecdysial tanning occurs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-020-0742-5) contains supplementary material, which is available to authorized users. BioMed Central 2020-02-19 /pmc/articles/PMC7029472/ /pubmed/32075655 http://dx.doi.org/10.1186/s12915-020-0742-5 Text en © The Author(s). 2020 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 Article
Flaven-Pouchon, Justin
Alvarez, Javier V.
Rojas, Candy
Ewer, John
The tanning hormone, bursicon, does not act directly on the epidermis to tan the Drosophila exoskeleton
title The tanning hormone, bursicon, does not act directly on the epidermis to tan the Drosophila exoskeleton
title_full The tanning hormone, bursicon, does not act directly on the epidermis to tan the Drosophila exoskeleton
title_fullStr The tanning hormone, bursicon, does not act directly on the epidermis to tan the Drosophila exoskeleton
title_full_unstemmed The tanning hormone, bursicon, does not act directly on the epidermis to tan the Drosophila exoskeleton
title_short The tanning hormone, bursicon, does not act directly on the epidermis to tan the Drosophila exoskeleton
title_sort tanning hormone, bursicon, does not act directly on the epidermis to tan the drosophila exoskeleton
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029472/
https://www.ncbi.nlm.nih.gov/pubmed/32075655
http://dx.doi.org/10.1186/s12915-020-0742-5
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