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Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints
BMP signaling plays a crucial role in the establishment of the dorso-ventral body axis in bilaterally symmetric animals. However, the topologies of the bone morphogenetic protein (BMP) signaling networks vary drastically in different animal groups, raising questions about the evolutionary constraint...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460265/ https://www.ncbi.nlm.nih.gov/pubmed/25772352 http://dx.doi.org/10.1016/j.celrep.2015.02.035 |
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author | Genikhovich, Grigory Fried, Patrick Prünster, M. Mandela Schinko, Johannes B. Gilles, Anna F. Fredman, David Meier, Karin Iber, Dagmar Technau, Ulrich |
author_facet | Genikhovich, Grigory Fried, Patrick Prünster, M. Mandela Schinko, Johannes B. Gilles, Anna F. Fredman, David Meier, Karin Iber, Dagmar Technau, Ulrich |
author_sort | Genikhovich, Grigory |
collection | PubMed |
description | BMP signaling plays a crucial role in the establishment of the dorso-ventral body axis in bilaterally symmetric animals. However, the topologies of the bone morphogenetic protein (BMP) signaling networks vary drastically in different animal groups, raising questions about the evolutionary constraints and evolvability of BMP signaling systems. Using loss-of-function analysis and mathematical modeling, we show that two signaling centers expressing different BMPs and BMP antagonists maintain the secondary axis of the sea anemone Nematostella. We demonstrate that BMP signaling is required for asymmetric Hox gene expression and mesentery formation. Computational analysis reveals that network parameters related to BMP4 and Chordin are constrained both in Nematostella and Xenopus, while those describing the BMP signaling modulators can vary significantly. Notably, only chordin, but not bmp4 expression needs to be spatially restricted for robust signaling gradient formation. Our data provide an explanation of the evolvability of BMP signaling systems in axis formation throughout Eumetazoa. |
format | Online Article Text |
id | pubmed-4460265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44602652015-06-16 Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints Genikhovich, Grigory Fried, Patrick Prünster, M. Mandela Schinko, Johannes B. Gilles, Anna F. Fredman, David Meier, Karin Iber, Dagmar Technau, Ulrich Cell Rep Report BMP signaling plays a crucial role in the establishment of the dorso-ventral body axis in bilaterally symmetric animals. However, the topologies of the bone morphogenetic protein (BMP) signaling networks vary drastically in different animal groups, raising questions about the evolutionary constraints and evolvability of BMP signaling systems. Using loss-of-function analysis and mathematical modeling, we show that two signaling centers expressing different BMPs and BMP antagonists maintain the secondary axis of the sea anemone Nematostella. We demonstrate that BMP signaling is required for asymmetric Hox gene expression and mesentery formation. Computational analysis reveals that network parameters related to BMP4 and Chordin are constrained both in Nematostella and Xenopus, while those describing the BMP signaling modulators can vary significantly. Notably, only chordin, but not bmp4 expression needs to be spatially restricted for robust signaling gradient formation. Our data provide an explanation of the evolvability of BMP signaling systems in axis formation throughout Eumetazoa. Cell Press 2015-03-12 /pmc/articles/PMC4460265/ /pubmed/25772352 http://dx.doi.org/10.1016/j.celrep.2015.02.035 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Report Genikhovich, Grigory Fried, Patrick Prünster, M. Mandela Schinko, Johannes B. Gilles, Anna F. Fredman, David Meier, Karin Iber, Dagmar Technau, Ulrich Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints |
title | Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints |
title_full | Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints |
title_fullStr | Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints |
title_full_unstemmed | Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints |
title_short | Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints |
title_sort | axis patterning by bmps: cnidarian network reveals evolutionary constraints |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460265/ https://www.ncbi.nlm.nih.gov/pubmed/25772352 http://dx.doi.org/10.1016/j.celrep.2015.02.035 |
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