Evidence map›Paper›PMID 39673176›Full record

ArticleMolecular biology and evolution2025

The Rich Evolutionary History of the Reactive Oxygen Species Metabolic Arsenal Shapes Its Mechanistic Plasticity at the Onset of Metazoan Regeneration.

Aurore Vullien, Aldine R Amiel, Loeiza Baduel, Dilara Diken, Cécile Renaud, Gabriel Krasovec, Michel Vervoort, Eric Röttinger, Eve Gazave

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Aurore VullienUniversité Paris Cité, CNRS, Institut Jacques Monod, F-75013 Paris, France.ORCID 0009-0002-5546-717X
Aldine R AmielUniversité Côte d'Azur, CNRS, INSERM, Institute for Research on Cancer and Aging, Nice (IRCAN), Nice, France.ORCID 0000-0002-3049-2822
Loeiza BaduelUniversité Paris Cité, CNRS, Institut Jacques Monod, F-75013 Paris, France.ORCID 0009-0004-1982-6117
Dilara DikenUniversité Côte d'Azur, CNRS, INSERM, Institute for Research on Cancer and Aging, Nice (IRCAN), Nice, France.ORCID 0000-0002-6903-7333
Cécile RenaudUniversité Paris Cité, CNRS, Institut Jacques Monod, F-75013 Paris, France.ORCID 0009-0007-4812-3455
Gabriel KrasovecUniversité Paris Cité, CNRS, Institut Jacques Monod, F-75013 Paris, France.ORCID 0000-0001-8848-2208
Michel VervoortUniversité Paris Cité, CNRS, Institut Jacques Monod, F-75013 Paris, France.ORCID 0000-0002-5995-2140
Eric RöttingerUniversité Côte d'Azur, CNRS, INSERM, Institute for Research on Cancer and Aging, Nice (IRCAN), Nice, France.ORCID 0000-0002-2938-6774
Eve GazaveUniversité Paris Cité, CNRS, Institut Jacques Monod, F-75013 Paris, France.ORCID 0000-0002-4647-6640

Funding

Agence Nationale de la Recherche ANR-11-IDEX-0005-01Association pour la Recherche sur le Cancer PJA 20191209482Centre National de la Recherche ScientifiqueCNRS Biologiecomité départemental de Paris de la Ligue Nationale Contre le Cancer RS20/75-20ENS Paris-SaclayFrench GovernmentLabex ANR-11-LABX-0071National Research Agency ANR-20-CE13-0014Université Paris Cité
6 · The paper itself

Abstract

Regeneration, the ability to restore body parts after injury, is widespread in metazoans; however, the underlying molecular and cellular mechanisms involved in this process remain largely unknown, and its evolutionary history is consequently unresolved. Recently, reactive oxygen species (ROS) have been shown in several metazoan models to be triggers of apoptosis and cell proliferation that drive regenerative success. However, it is not known whether the contribution of ROS to regeneration relies on conserved mechanisms. Here we performed a comparative genomic analysis of ROS metabolism actors across metazoans, and carried out a comparative study of the deployment and roles of ROS during regeneration in two different metazoan models: the annelid Platynereis dumerilii and the cnidarian Nematostella vectensis. We established that the vast majority of metazoans encode a core redox kit allowing for the production and detoxification of ROS, and overall regulation of ROS levels. However, the precise composition of the redox arsenal can vary significantly from species to species, suggesting that evolutionary constraints apply to ROS metabolism functions rather than precise actors. We found that while ROS are necessary for regeneration in both Platynereis and Nematostella, the two species deploy different enzymatic activities controlling ROS dynamics, and display distinct effects of ROS signaling on injury-induced apoptosis and cell proliferation. We conclude that, while ROS are a common feature of metazoan regeneration, their production and contribution to this phenomenon may depend on different molecular mechanisms highlighting the overall plasticity of the machinery.

Indexed as

Reactive Oxygen SpeciesRegenerationAnimalsBiological EvolutionPolychaetaSea AnemonesReactive Oxygen Speciesannelidapoptosiscnidariancomparative genomicsNematostellaPlatynereisproliferationreactive oxygen species (ROS)regeneration

Identifiers

PMID39673176
PMCPMC11721785

What Socratic holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.