Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in <i>Hydra</i> 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 <i>Hydra</i>. Axis polarity is strongly me...

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Main Authors: Lital Shani-Zerbib, Liora Garion, Yonit Maroudas-Sacks, Erez Braun, Kinneret Keren
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/13/2/360
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author Lital Shani-Zerbib
Liora Garion
Yonit Maroudas-Sacks
Erez Braun
Kinneret Keren
author_facet Lital Shani-Zerbib
Liora Garion
Yonit Maroudas-Sacks
Erez Braun
Kinneret Keren
author_sort Lital Shani-Zerbib
collection DOAJ
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 <i>Hydra</i>. Axis polarity is strongly memorized in <i>Hydra</i> 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. <i>Hydra</i> 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 doaj.art-b31358fc034f42549b18f6cfed8c75ea2023-11-23T20:05:39ZengMDPI AGGenes2073-44252022-02-0113236010.3390/genes13020360Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in <i>Hydra</i> RegenerationLital Shani-Zerbib0Liora Garion1Yonit Maroudas-Sacks2Erez Braun3Kinneret Keren4Department of Physics, Technion—Israel Institute of Technology, Haifa 32000, IsraelDepartment of Physics, Technion—Israel Institute of Technology, Haifa 32000, IsraelDepartment of Physics, Technion—Israel Institute of Technology, Haifa 32000, IsraelDepartment of Physics, Technion—Israel Institute of Technology, Haifa 32000, IsraelDepartment of Physics, Technion—Israel Institute of Technology, Haifa 32000, IsraelThe 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 <i>Hydra</i>. Axis polarity is strongly memorized in <i>Hydra</i> 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. <i>Hydra</i> 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.https://www.mdpi.com/2073-4425/13/2/360<i>Hydra</i> regenerationbody axis polaritymorphogenesissupracellular actin fiberstopological defects
spellingShingle Lital Shani-Zerbib
Liora Garion
Yonit Maroudas-Sacks
Erez Braun
Kinneret Keren
Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in <i>Hydra</i> Regeneration
Genes
<i>Hydra</i> regeneration
body axis polarity
morphogenesis
supracellular actin fibers
topological defects
title Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in <i>Hydra</i> Regeneration
title_full Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in <i>Hydra</i> Regeneration
title_fullStr Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in <i>Hydra</i> Regeneration
title_full_unstemmed Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in <i>Hydra</i> Regeneration
title_short Canalized Morphogenesis Driven by Inherited Tissue Asymmetries in <i>Hydra</i> Regeneration
title_sort canalized morphogenesis driven by inherited tissue asymmetries in i hydra i regeneration
topic <i>Hydra</i> regeneration
body axis polarity
morphogenesis
supracellular actin fibers
topological defects
url https://www.mdpi.com/2073-4425/13/2/360
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AT yonitmaroudassacks canalizedmorphogenesisdrivenbyinheritedtissueasymmetriesinihydrairegeneration
AT erezbraun canalizedmorphogenesisdrivenbyinheritedtissueasymmetriesinihydrairegeneration
AT kinneretkeren canalizedmorphogenesisdrivenbyinheritedtissueasymmetriesinihydrairegeneration