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Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in Hydra Regeneration

The emergence and stabilization of a body axis is a major step in animal morphogenesis, determining the symmetry of the body plan as well as its polarity. To advance our understanding of the emergence of body axis polarity, we study regenerating Hydra. Axis polarity is strongly memorized in Hydra re...

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Autores principales: Shani-Zerbib, Lital, Garion, Liora, Maroudas-Sacks, Yonit, Braun, Erez, Keren, Kinneret
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8872179/
https://www.ncbi.nlm.nih.gov/pubmed/35205404
http://dx.doi.org/10.3390/genes13020360
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author Shani-Zerbib, Lital
Garion, Liora
Maroudas-Sacks, Yonit
Braun, Erez
Keren, Kinneret
author_facet Shani-Zerbib, Lital
Garion, Liora
Maroudas-Sacks, Yonit
Braun, Erez
Keren, Kinneret
author_sort Shani-Zerbib, Lital
collection PubMed
description The emergence and stabilization of a body axis is a major step in animal morphogenesis, determining the symmetry of the body plan as well as its polarity. To advance our understanding of the emergence of body axis polarity, we study regenerating Hydra. Axis polarity is strongly memorized in Hydra regeneration even in small tissue segments. What type of processes confer this memory? To gain insight into the emerging polarity, we utilize frustrating initial conditions by studying regenerating tissue strips which fold into hollow spheroids by adhering their distal ends of opposite original polarities. Despite the convoluted folding process and the tissue rearrangements during regeneration, these tissue strips develop in a reproducible manner, preserving the original polarity and yielding an ordered body plan. These observations suggest that the integration of mechanical and biochemical processes supported by their mutual feedback attracts the tissue dynamics towards a well-defined developmental trajectory biased by weak inherited cues from the parent animal. Hydra thus provide an example of dynamic canalization in which the dynamic rules are instilled, but, in contrast to the classical picture, the detailed developmental trajectory does not unfold in a programmatic manner.
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spelling pubmed-88721792022-02-25 Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in Hydra Regeneration Shani-Zerbib, Lital Garion, Liora Maroudas-Sacks, Yonit Braun, Erez Keren, Kinneret Genes (Basel) Article The emergence and stabilization of a body axis is a major step in animal morphogenesis, determining the symmetry of the body plan as well as its polarity. To advance our understanding of the emergence of body axis polarity, we study regenerating Hydra. Axis polarity is strongly memorized in Hydra regeneration even in small tissue segments. What type of processes confer this memory? To gain insight into the emerging polarity, we utilize frustrating initial conditions by studying regenerating tissue strips which fold into hollow spheroids by adhering their distal ends of opposite original polarities. Despite the convoluted folding process and the tissue rearrangements during regeneration, these tissue strips develop in a reproducible manner, preserving the original polarity and yielding an ordered body plan. These observations suggest that the integration of mechanical and biochemical processes supported by their mutual feedback attracts the tissue dynamics towards a well-defined developmental trajectory biased by weak inherited cues from the parent animal. Hydra thus provide an example of dynamic canalization in which the dynamic rules are instilled, but, in contrast to the classical picture, the detailed developmental trajectory does not unfold in a programmatic manner. MDPI 2022-02-16 /pmc/articles/PMC8872179/ /pubmed/35205404 http://dx.doi.org/10.3390/genes13020360 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shani-Zerbib, Lital
Garion, Liora
Maroudas-Sacks, Yonit
Braun, Erez
Keren, Kinneret
Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in Hydra Regeneration
title Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in Hydra Regeneration
title_full Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in Hydra Regeneration
title_fullStr Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in Hydra Regeneration
title_full_unstemmed Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in Hydra Regeneration
title_short Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in Hydra Regeneration
title_sort canalized morphogenesis driven by inherited tissue asymmetries in hydra regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8872179/
https://www.ncbi.nlm.nih.gov/pubmed/35205404
http://dx.doi.org/10.3390/genes13020360
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