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Striking parallels between dorsoventral patterning in Drosophila and Gryllus reveal a complex evolutionary history behind a model gene regulatory network
Dorsoventral pattering relies on Toll and BMP signalling in all insects studied so far, with variations in the relative contributions of both pathways. Drosophila and the beetle Tribolium share extensive dependence on Toll, while representatives of more distantly related lineages like the wasp Nason...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051952/ https://www.ncbi.nlm.nih.gov/pubmed/33783353 http://dx.doi.org/10.7554/eLife.68287 |
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author | Pechmann, Matthias Kenny, Nathan James Pott, Laura Heger, Peter Chen, Yen-Ta Buchta, Thomas Özüak, Orhan Lynch, Jeremy Roth, Siegfried |
author_facet | Pechmann, Matthias Kenny, Nathan James Pott, Laura Heger, Peter Chen, Yen-Ta Buchta, Thomas Özüak, Orhan Lynch, Jeremy Roth, Siegfried |
author_sort | Pechmann, Matthias |
collection | PubMed |
description | Dorsoventral pattering relies on Toll and BMP signalling in all insects studied so far, with variations in the relative contributions of both pathways. Drosophila and the beetle Tribolium share extensive dependence on Toll, while representatives of more distantly related lineages like the wasp Nasonia and bug Oncopeltus rely more strongly on BMP signalling. Here, we show that in the cricket Gryllus bimaculatus, an evolutionarily distant outgroup, Toll has, like in Drosophila, a direct patterning role for the ventral half of the embryo. In addition, Toll polarises BMP signalling, although this does not involve the conserved BMP inhibitor Sog/Chordin. Finally, Toll activation relies on ovarian patterning mechanisms with striking similarity to Drosophila. Our data suggest two surprising hypotheses: (1) that Toll's patterning function in Gryllus and Drosophila is the result of convergent evolution or (2) a Drosophila-like system arose early in insect evolution and was extensively altered in multiple independent lineages. |
format | Online Article Text |
id | pubmed-8051952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-80519522021-04-21 Striking parallels between dorsoventral patterning in Drosophila and Gryllus reveal a complex evolutionary history behind a model gene regulatory network Pechmann, Matthias Kenny, Nathan James Pott, Laura Heger, Peter Chen, Yen-Ta Buchta, Thomas Özüak, Orhan Lynch, Jeremy Roth, Siegfried eLife Evolutionary Biology Dorsoventral pattering relies on Toll and BMP signalling in all insects studied so far, with variations in the relative contributions of both pathways. Drosophila and the beetle Tribolium share extensive dependence on Toll, while representatives of more distantly related lineages like the wasp Nasonia and bug Oncopeltus rely more strongly on BMP signalling. Here, we show that in the cricket Gryllus bimaculatus, an evolutionarily distant outgroup, Toll has, like in Drosophila, a direct patterning role for the ventral half of the embryo. In addition, Toll polarises BMP signalling, although this does not involve the conserved BMP inhibitor Sog/Chordin. Finally, Toll activation relies on ovarian patterning mechanisms with striking similarity to Drosophila. Our data suggest two surprising hypotheses: (1) that Toll's patterning function in Gryllus and Drosophila is the result of convergent evolution or (2) a Drosophila-like system arose early in insect evolution and was extensively altered in multiple independent lineages. eLife Sciences Publications, Ltd 2021-03-30 /pmc/articles/PMC8051952/ /pubmed/33783353 http://dx.doi.org/10.7554/eLife.68287 Text en © 2021, Pechmann et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Evolutionary Biology Pechmann, Matthias Kenny, Nathan James Pott, Laura Heger, Peter Chen, Yen-Ta Buchta, Thomas Özüak, Orhan Lynch, Jeremy Roth, Siegfried Striking parallels between dorsoventral patterning in Drosophila and Gryllus reveal a complex evolutionary history behind a model gene regulatory network |
title | Striking parallels between dorsoventral patterning in Drosophila and Gryllus reveal a complex evolutionary history behind a model gene regulatory network |
title_full | Striking parallels between dorsoventral patterning in Drosophila and Gryllus reveal a complex evolutionary history behind a model gene regulatory network |
title_fullStr | Striking parallels between dorsoventral patterning in Drosophila and Gryllus reveal a complex evolutionary history behind a model gene regulatory network |
title_full_unstemmed | Striking parallels between dorsoventral patterning in Drosophila and Gryllus reveal a complex evolutionary history behind a model gene regulatory network |
title_short | Striking parallels between dorsoventral patterning in Drosophila and Gryllus reveal a complex evolutionary history behind a model gene regulatory network |
title_sort | striking parallels between dorsoventral patterning in drosophila and gryllus reveal a complex evolutionary history behind a model gene regulatory network |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051952/ https://www.ncbi.nlm.nih.gov/pubmed/33783353 http://dx.doi.org/10.7554/eLife.68287 |
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