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Structural conservation of insulin/IGF signalling axis at the insulin receptors level in Drosophila and humans
The insulin-related hormones regulate key life processes in Metazoa, from metabolism to growth, lifespan and aging, through an evolutionarily conserved insulin signalling axis (IIS). In humans the IIS axis is controlled by insulin, two insulin-like growth factors, two isoforms of the insulin recepto...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560217/ https://www.ncbi.nlm.nih.gov/pubmed/37805602 http://dx.doi.org/10.1038/s41467-023-41862-x |
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author | Viola, Cristina M. Frittmann, Orsolya Jenkins, Huw T. Shafi, Talha De Meyts, Pierre Brzozowski, Andrzej M. |
author_facet | Viola, Cristina M. Frittmann, Orsolya Jenkins, Huw T. Shafi, Talha De Meyts, Pierre Brzozowski, Andrzej M. |
author_sort | Viola, Cristina M. |
collection | PubMed |
description | The insulin-related hormones regulate key life processes in Metazoa, from metabolism to growth, lifespan and aging, through an evolutionarily conserved insulin signalling axis (IIS). In humans the IIS axis is controlled by insulin, two insulin-like growth factors, two isoforms of the insulin receptor (hIR-A and -B), and its homologous IGF-1R. In Drosophila, this signalling engages seven insulin-like hormones (DILP1-7) and a single receptor (dmIR). This report describes the cryoEM structure of the dmIR ectodomain:DILP5 complex, revealing high structural homology between dmIR and hIR. The excess of DILP5 yields dmIR complex in an asymmetric ‘T’ conformation, similar to that observed in some complexes of human IRs. However, dmIR binds three DILP5 molecules in a distinct arrangement, showing also dmIR-specific features. This work adds structural support to evolutionary conservation of the IIS axis at the IR level, and also underpins a better understanding of an important model organism. |
format | Online Article Text |
id | pubmed-10560217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105602172023-10-09 Structural conservation of insulin/IGF signalling axis at the insulin receptors level in Drosophila and humans Viola, Cristina M. Frittmann, Orsolya Jenkins, Huw T. Shafi, Talha De Meyts, Pierre Brzozowski, Andrzej M. Nat Commun Article The insulin-related hormones regulate key life processes in Metazoa, from metabolism to growth, lifespan and aging, through an evolutionarily conserved insulin signalling axis (IIS). In humans the IIS axis is controlled by insulin, two insulin-like growth factors, two isoforms of the insulin receptor (hIR-A and -B), and its homologous IGF-1R. In Drosophila, this signalling engages seven insulin-like hormones (DILP1-7) and a single receptor (dmIR). This report describes the cryoEM structure of the dmIR ectodomain:DILP5 complex, revealing high structural homology between dmIR and hIR. The excess of DILP5 yields dmIR complex in an asymmetric ‘T’ conformation, similar to that observed in some complexes of human IRs. However, dmIR binds three DILP5 molecules in a distinct arrangement, showing also dmIR-specific features. This work adds structural support to evolutionary conservation of the IIS axis at the IR level, and also underpins a better understanding of an important model organism. Nature Publishing Group UK 2023-10-07 /pmc/articles/PMC10560217/ /pubmed/37805602 http://dx.doi.org/10.1038/s41467-023-41862-x Text en © The Author(s) 2023 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 Viola, Cristina M. Frittmann, Orsolya Jenkins, Huw T. Shafi, Talha De Meyts, Pierre Brzozowski, Andrzej M. Structural conservation of insulin/IGF signalling axis at the insulin receptors level in Drosophila and humans |
title | Structural conservation of insulin/IGF signalling axis at the insulin receptors level in Drosophila and humans |
title_full | Structural conservation of insulin/IGF signalling axis at the insulin receptors level in Drosophila and humans |
title_fullStr | Structural conservation of insulin/IGF signalling axis at the insulin receptors level in Drosophila and humans |
title_full_unstemmed | Structural conservation of insulin/IGF signalling axis at the insulin receptors level in Drosophila and humans |
title_short | Structural conservation of insulin/IGF signalling axis at the insulin receptors level in Drosophila and humans |
title_sort | structural conservation of insulin/igf signalling axis at the insulin receptors level in drosophila and humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560217/ https://www.ncbi.nlm.nih.gov/pubmed/37805602 http://dx.doi.org/10.1038/s41467-023-41862-x |
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