Validation of metaxin-2 deficient C. elegans as a model for MandibuloAcral Dysplasia associated to mtx-2 (MADaM) syndrome

MandibuloAcral Dysplasia associated to MTX2 gene (MADaM) is a recently described progeroid syndrome (accelerated aging disease) whose clinical manifestations include skin abnormalities, growth retardation, and cardiovascular diseases. We previously proposed that mtx-2-deficient C. elegans could be used as a model for MADaM and to support this, we present here our comprehensive phenotypic characterization of these worms using atomic force microscopy (AFM), transcriptomic, and oxygen consumption rate analyses. AFM analysis showed that young mtx-2-less worms had a significantly rougher, less elastic cuticle which becomes significantly rougher and less elastic as they age, and abnormal mitochondrial morphology. mtx-2 C. elegans displayed slightly delayed development, decreased pharyngeal pumping, significantly reduced mitochondrial respiratory capacities, and transcriptomic analysis identified perturbations in the aging, TOR, and WNT-signaling pathways. The phenotypic characteristics of mtx-2 worms shown here are analogous to many of the human clinical presentations of MADaM and we believe this validates their use as a model which will allow us to uncover the molecular details of the disease and develop new therapeutics and treatments.

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Publication Details

Journal
Communications Biology
Published
2024-10-26
DOI
https://doi.org/10.1038/s42003-024-06967-z
Citations
3
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
0.68

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article

Validation of metaxin-2 deficient C. elegans as a model for MandibuloAcral Dysplasia associated to mtx-2 (MADaM) syndrome

Bénédicte Thiébot, Georges Smolyakov, Homa Adle‐Biassette, Chloé Talarmin et al.
3 citations
Communications Biology
Genetics, Aging, and Longevity in Model Organisms
0.68
article

Validation of metaxin-2 deficient C. elegans as a model for MandibuloAcral Dysplasia associated to mtx-2 (MADaM) syndrome

Bénédicte Thiébot, Georges Smolyakov, Homa Adle‐Biassette, Chloé Talarmin, Song-Hua Lee, Cyril Scandola, Cleo Parisi, Philippe Manivet, Timothy Ganderton, Valérie Andrianasolonirina, Cloé Lecoq, Valentine Houtart
article en
3 citations

Abstract

MandibuloAcral Dysplasia associated to MTX2 gene (MADaM) is a recently described progeroid syndrome (accelerated aging disease) whose clinical manifestations include skin abnormalities, growth retardation, and cardiovascular diseases. We previously proposed that mtx-2-deficient C. elegans could be used as a model for MADaM and to support this, we present here our comprehensive phenotypic characterization of these worms using atomic force microscopy (AFM), transcriptomic, and oxygen consumption rate analyses. AFM analysis showed that young mtx-2-less worms had a significantly rougher, less elastic cuticle which becomes significantly rougher and less elastic as they age, and abnormal mitochondrial morphology. mtx-2 C. elegans displayed slightly delayed development, decreased pharyngeal pumping, significantly reduced mitochondrial respiratory capacities, and transcriptomic analysis identified perturbations in the aging, TOR, and WNT-signaling pathways. The phenotypic characteristics of mtx-2 worms shown here are analogous to many of the human clinical presentations of MADaM and we believe this validates their use as a model which will allow us to uncover the molecular details of the disease and develop new therapeutics and treatments.

Communications BiologyVol. 7(1)
Délégation Paris 5 (FR), Centre National de la Recherche Scientifique (FR), Inserm (FR), Institut Pasteur (FR), Délégation Paris 7 (FR), Université Paris Cité (FR), Université Paris-Saclay (FR), Assistance Publique – Hôpitaux de Paris (FR), Hôpital Lariboisière (FR), Celescreen (France) (FR), CY Cergy Paris Université (FR), NeuroDiderot (FR)
Aix-Marseille Université, Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Servier
Zero hunger
Openalex Percentile: Top 32%
Genetics, Aging, and Longevity in Model Organisms
0.68
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