Whole body regeneration deploys a rewired embryonic gene regulatory network logic.

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Auteurs principaux: Andreoni-Pham, Rita, Johnston, Hereroa, Warner, Jacob F, Nedoncelle, Karine, Carvalho, João E, Hofmänner, Kai, Maugeri, Agata, Croce, Olivier, Amiel, Aldine R, Röttinger, Eric
Format: Artículo científico
Langue:en
Publié: Nature communications 2025
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author Andreoni-Pham, Rita
Johnston, Hereroa
Warner, Jacob F
Nedoncelle, Karine
Carvalho, João E
Hofmänner, Kai
Maugeri, Agata
Croce, Olivier
Amiel, Aldine R
Röttinger, Eric
author_facet Andreoni-Pham, Rita
Johnston, Hereroa
Warner, Jacob F
Nedoncelle, Karine
Carvalho, João E
Hofmänner, Kai
Maugeri, Agata
Croce, Olivier
Amiel, Aldine R
Röttinger, Eric
Andreoni-Pham, Rita
Johnston, Hereroa
Warner, Jacob F
Nedoncelle, Karine
Carvalho, João E
Hofmänner, Kai
Maugeri, Agata
Croce, Olivier
Amiel, Aldine R
Röttinger, Eric
collection PubMed - marine biology
contents Whole body regeneration deploys a rewired embryonic gene regulatory network logic. Andreoni-Pham, Rita Johnston, Hereroa Warner, Jacob F Nedoncelle, Karine Carvalho, João E Hofmänner, Kai Maugeri, Agata Croce, Olivier Amiel, Aldine R Röttinger, Eric Animals Regeneration Gene Regulatory Networks Gene Expression Regulation, Developmental Sea Anemones Apoptosis Signal Transduction Transcriptome Embryo, Nonmammalian Embryonic Development Gene Expression Profiling A long-held hypothesis in regeneration proposes that developmental processes are re-deployed during regeneration. To investigate this, we compared embryonic and regeneration gene regulatory networks (GRN) in the sea anemone Nematostella vectensis using transcriptomic time series spanning these two developmental trajectories. Here, we show that regeneration reuses cohorts of the embryonic genes along with a small set of genes whose expression dynamics are specific to regeneration. We identified co-expression modules that are either conserved between embryogenesis and regeneration or specific to regeneration, with the latter linked to cellular mechanisms such as apoptosis, tissue remodeling, and wound healing. Functional assays revealed that apoptosis and cWnt signaling pathways are partially MEK/ERK dependent, have largely distinct downstream targets but converge to coordinate regenerative responses. Collectively, these results indicate that regeneration in N. vectensis represents a partial redeployment and extensive rewiring of the embryonic GRN, reactivating developmental modules through a regeneration-specific network logic.
format Artículo científico
id pubmed_41381581
institution PubMed
language en
publishDate 2025
publisher Nature communications
record_format pubmed
spellingShingle Whole body regeneration deploys a rewired embryonic gene regulatory network logic.
Andreoni-Pham, Rita
Johnston, Hereroa
Warner, Jacob F
Nedoncelle, Karine
Carvalho, João E
Hofmänner, Kai
Maugeri, Agata
Croce, Olivier
Amiel, Aldine R
Röttinger, Eric
Animals
Regeneration
Gene Regulatory Networks
Gene Expression Regulation, Developmental
Sea Anemones
Apoptosis
Signal Transduction
Transcriptome
Embryo, Nonmammalian
Embryonic Development
Gene Expression Profiling
Whole body regeneration deploys a rewired embryonic gene regulatory network logic. Andreoni-Pham, Rita Johnston, Hereroa Warner, Jacob F Nedoncelle, Karine Carvalho, João E Hofmänner, Kai Maugeri, Agata Croce, Olivier Amiel, Aldine R Röttinger, Eric Animals Regeneration Gene Regulatory Networks Gene Expression Regulation, Developmental Sea Anemones Apoptosis Signal Transduction Transcriptome Embryo, Nonmammalian Embryonic Development Gene Expression Profiling A long-held hypothesis in regeneration proposes that developmental processes are re-deployed during regeneration. To investigate this, we compared embryonic and regeneration gene regulatory networks (GRN) in the sea anemone Nematostella vectensis using transcriptomic time series spanning these two developmental trajectories. Here, we show that regeneration reuses cohorts of the embryonic genes along with a small set of genes whose expression dynamics are specific to regeneration. We identified co-expression modules that are either conserved between embryogenesis and regeneration or specific to regeneration, with the latter linked to cellular mechanisms such as apoptosis, tissue remodeling, and wound healing. Functional assays revealed that apoptosis and cWnt signaling pathways are partially MEK/ERK dependent, have largely distinct downstream targets but converge to coordinate regenerative responses. Collectively, these results indicate that regeneration in N. vectensis represents a partial redeployment and extensive rewiring of the embryonic GRN, reactivating developmental modules through a regeneration-specific network logic.
title Whole body regeneration deploys a rewired embryonic gene regulatory network logic.
topic Animals
Regeneration
Gene Regulatory Networks
Gene Expression Regulation, Developmental
Sea Anemones
Apoptosis
Signal Transduction
Transcriptome
Embryo, Nonmammalian
Embryonic Development
Gene Expression Profiling
url https://pubmed.ncbi.nlm.nih.gov/41381581/