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Evolution‐development congruence in pattern formation dynamics: Bifurcations in gene expression and regulation of networks structures

Search for possible relationships between phylogeny and ontogeny is important in evolutionary‐developmental biology. Here we uncover such relationships by numerical evolution and unveil their origin in terms of dynamical systems theory. By representing developmental dynamics of spatially located cel...

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Autores principales: Kohsokabe, Takahiro, Kaneko, Kunihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064737/
https://www.ncbi.nlm.nih.gov/pubmed/26678220
http://dx.doi.org/10.1002/jez.b.22666
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author Kohsokabe, Takahiro
Kaneko, Kunihiko
author_facet Kohsokabe, Takahiro
Kaneko, Kunihiko
author_sort Kohsokabe, Takahiro
collection PubMed
description Search for possible relationships between phylogeny and ontogeny is important in evolutionary‐developmental biology. Here we uncover such relationships by numerical evolution and unveil their origin in terms of dynamical systems theory. By representing developmental dynamics of spatially located cells with gene expression dynamics with cell‐to‐cell interaction under external morphogen gradient, gene regulation networks are evolved under mutation and selection with the fitness to approach a prescribed spatial pattern of expressed genes. For most numerical evolution experiments, evolution of pattern over generations and development of pattern by an evolved network exhibit remarkable congruence. Both in the evolution and development pattern changes consist of several epochs where stripes are formed in a short time, while for other temporal regimes, pattern hardly changes. In evolution, these quasi‐stationary regimes are generations needed to hit relevant mutations, while in development, they are due to some gene expression that varies slowly and controls the pattern change. The morphogenesis is regulated by combinations of feedback or feedforward regulations, where the upstream feedforward network reads the external morphogen gradient, and generates a pattern used as a boundary condition for the later patterns. The ordering from up to downstream is common in evolution and development, while the successive epochal changes in development and evolution are represented as common bifurcations in dynamical‐systems theory, which lead to the evolution‐development congruence. Mechanism of exceptional violation of the congruence is also unveiled. Our results provide a new look on developmental stages, punctuated equilibrium, developmental bottlenecks, and evolutionary acquisition of novelty in morphogenesis. J. Exp. Zool. (Mol. Dev. Evol.) 326B:61–84, 2016. © 2015 The Authors. Journal of Experimental Zoology Part B: Molecular and Developmental Evolution Published by Wiley Periodicals, Inc.
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spelling pubmed-50647372016-10-19 Evolution‐development congruence in pattern formation dynamics: Bifurcations in gene expression and regulation of networks structures Kohsokabe, Takahiro Kaneko, Kunihiko J Exp Zool B Mol Dev Evol Research Articles Search for possible relationships between phylogeny and ontogeny is important in evolutionary‐developmental biology. Here we uncover such relationships by numerical evolution and unveil their origin in terms of dynamical systems theory. By representing developmental dynamics of spatially located cells with gene expression dynamics with cell‐to‐cell interaction under external morphogen gradient, gene regulation networks are evolved under mutation and selection with the fitness to approach a prescribed spatial pattern of expressed genes. For most numerical evolution experiments, evolution of pattern over generations and development of pattern by an evolved network exhibit remarkable congruence. Both in the evolution and development pattern changes consist of several epochs where stripes are formed in a short time, while for other temporal regimes, pattern hardly changes. In evolution, these quasi‐stationary regimes are generations needed to hit relevant mutations, while in development, they are due to some gene expression that varies slowly and controls the pattern change. The morphogenesis is regulated by combinations of feedback or feedforward regulations, where the upstream feedforward network reads the external morphogen gradient, and generates a pattern used as a boundary condition for the later patterns. The ordering from up to downstream is common in evolution and development, while the successive epochal changes in development and evolution are represented as common bifurcations in dynamical‐systems theory, which lead to the evolution‐development congruence. Mechanism of exceptional violation of the congruence is also unveiled. Our results provide a new look on developmental stages, punctuated equilibrium, developmental bottlenecks, and evolutionary acquisition of novelty in morphogenesis. J. Exp. Zool. (Mol. Dev. Evol.) 326B:61–84, 2016. © 2015 The Authors. Journal of Experimental Zoology Part B: Molecular and Developmental Evolution Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2016-01 2015-12-17 /pmc/articles/PMC5064737/ /pubmed/26678220 http://dx.doi.org/10.1002/jez.b.22666 Text en © 2015 The Authors. Journal of Experimental Zoology Part B: Molecular and Developmental Evolution Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Kohsokabe, Takahiro
Kaneko, Kunihiko
Evolution‐development congruence in pattern formation dynamics: Bifurcations in gene expression and regulation of networks structures
title Evolution‐development congruence in pattern formation dynamics: Bifurcations in gene expression and regulation of networks structures
title_full Evolution‐development congruence in pattern formation dynamics: Bifurcations in gene expression and regulation of networks structures
title_fullStr Evolution‐development congruence in pattern formation dynamics: Bifurcations in gene expression and regulation of networks structures
title_full_unstemmed Evolution‐development congruence in pattern formation dynamics: Bifurcations in gene expression and regulation of networks structures
title_short Evolution‐development congruence in pattern formation dynamics: Bifurcations in gene expression and regulation of networks structures
title_sort evolution‐development congruence in pattern formation dynamics: bifurcations in gene expression and regulation of networks structures
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064737/
https://www.ncbi.nlm.nih.gov/pubmed/26678220
http://dx.doi.org/10.1002/jez.b.22666
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