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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...

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Autores principales: Pechmann, Matthias, Kenny, Nathan James, Pott, Laura, Heger, Peter, Chen, Yen-Ta, Buchta, Thomas, Özüak, Orhan, Lynch, Jeremy, Roth, Siegfried
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
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.
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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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