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Interlocking of co-opted developmental gene networks in Drosophila and the evolution of pre-adaptive novelty
The re-use of genes in new organs forms the base of many evolutionary novelties. A well-characterised case is the recruitment of the posterior spiracle gene network to the Drosophila male genitalia. Here we find that this network has also been co-opted to the testis mesoderm where is required for sp...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504328/ https://www.ncbi.nlm.nih.gov/pubmed/37714829 http://dx.doi.org/10.1038/s41467-023-41414-3 |
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author | Molina-Gil, Sara Sotillos, Sol Espinosa-Vázquez, José Manuel Almudi, Isabel Hombría, James C.-G. |
author_facet | Molina-Gil, Sara Sotillos, Sol Espinosa-Vázquez, José Manuel Almudi, Isabel Hombría, James C.-G. |
author_sort | Molina-Gil, Sara |
collection | PubMed |
description | The re-use of genes in new organs forms the base of many evolutionary novelties. A well-characterised case is the recruitment of the posterior spiracle gene network to the Drosophila male genitalia. Here we find that this network has also been co-opted to the testis mesoderm where is required for sperm liberation, providing an example of sequentially repeated developmental co-options. Associated to this co-option event, an evolutionary expression novelty appeared, the activation of the posterior segment determinant Engrailed to the anterior A8 segment controlled by common testis and spiracle regulatory elements. Enhancer deletion shows that A8 anterior Engrailed activation is not required for spiracle development but only necessary in the testis. Our study presents an example of pre-adaptive developmental novelty: the activation of the Engrailed transcription factor in the anterior compartment of the A8 segment where, despite having no specific function, opens the possibility of this developmental factor acquiring one. We propose that recently co-opted networks become interlocked, so that any change to the network because of its function in one organ, will be mirrored by other organs even if it provides no selective advantage to them. |
format | Online Article Text |
id | pubmed-10504328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105043282023-09-17 Interlocking of co-opted developmental gene networks in Drosophila and the evolution of pre-adaptive novelty Molina-Gil, Sara Sotillos, Sol Espinosa-Vázquez, José Manuel Almudi, Isabel Hombría, James C.-G. Nat Commun Article The re-use of genes in new organs forms the base of many evolutionary novelties. A well-characterised case is the recruitment of the posterior spiracle gene network to the Drosophila male genitalia. Here we find that this network has also been co-opted to the testis mesoderm where is required for sperm liberation, providing an example of sequentially repeated developmental co-options. Associated to this co-option event, an evolutionary expression novelty appeared, the activation of the posterior segment determinant Engrailed to the anterior A8 segment controlled by common testis and spiracle regulatory elements. Enhancer deletion shows that A8 anterior Engrailed activation is not required for spiracle development but only necessary in the testis. Our study presents an example of pre-adaptive developmental novelty: the activation of the Engrailed transcription factor in the anterior compartment of the A8 segment where, despite having no specific function, opens the possibility of this developmental factor acquiring one. We propose that recently co-opted networks become interlocked, so that any change to the network because of its function in one organ, will be mirrored by other organs even if it provides no selective advantage to them. Nature Publishing Group UK 2023-09-15 /pmc/articles/PMC10504328/ /pubmed/37714829 http://dx.doi.org/10.1038/s41467-023-41414-3 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 Molina-Gil, Sara Sotillos, Sol Espinosa-Vázquez, José Manuel Almudi, Isabel Hombría, James C.-G. Interlocking of co-opted developmental gene networks in Drosophila and the evolution of pre-adaptive novelty |
title | Interlocking of co-opted developmental gene networks in Drosophila and the evolution of pre-adaptive novelty |
title_full | Interlocking of co-opted developmental gene networks in Drosophila and the evolution of pre-adaptive novelty |
title_fullStr | Interlocking of co-opted developmental gene networks in Drosophila and the evolution of pre-adaptive novelty |
title_full_unstemmed | Interlocking of co-opted developmental gene networks in Drosophila and the evolution of pre-adaptive novelty |
title_short | Interlocking of co-opted developmental gene networks in Drosophila and the evolution of pre-adaptive novelty |
title_sort | interlocking of co-opted developmental gene networks in drosophila and the evolution of pre-adaptive novelty |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504328/ https://www.ncbi.nlm.nih.gov/pubmed/37714829 http://dx.doi.org/10.1038/s41467-023-41414-3 |
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