DYRK1A roles in human neural progenitors

Together, the DYRK1A interactome in hNSCs and the gene expression changes induced by its depletion highlight the significant role of DYRK1A in regulating hNSC proliferation. Although the effects on various growth signaling pathways may appear contradictory, the overall impact is a marked reduction in hNSC proliferation. This research underscores the pivotal role of DYRK1A in neurodevelopment and identifies, among DYRK1A's protein partners and differentially expressed genes, potential novel candidate genes for NDDs and promising therapeutic targets for DYRK1A syndrome.

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Publication Details

Journal
Frontiers in Neuroscience
Published
2025-03-13
DOI
https://doi.org/10.3389/fnins.2025.1533253
Citations
5
Primary Topic
Down syndrome and intellectual disability research
Type
article
Field-Weighted Citation Impact
9.39

Funders

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DYRK1A roles in human neural progenitors

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Down syndrome and intellectual disability research
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DYRK1A roles in human neural progenitors

Nathalie Drouot, Alexandra Benchoua, Irene Zapata-Bodalo, Amélie Piton, Johan Gilet, Angélique Quartier, Jérémie Courraud, Jean-Louis Mandel
article en
5 citations

Abstract

Together, the DYRK1A interactome in hNSCs and the gene expression changes induced by its depletion highlight the significant role of DYRK1A in regulating hNSC proliferation. Although the effects on various growth signaling pathways may appear contradictory, the overall impact is a marked reduction in hNSC proliferation. This research underscores the pivotal role of DYRK1A in neurodevelopment and identifies, among DYRK1A's protein partners and differentially expressed genes, potential novel candidate genes for NDDs and promising therapeutic targets for DYRK1A syndrome.

Frontiers in NeuroscienceVol. 19
Centre National de la Recherche Scientifique (FR), Inserm (FR), Institut Universitaire de France (FR), Institut de génétique et de biologie moléculaire et cellulaire (FR), Institut National de Recherche en Santé Publique (ML), Institut des Cellules Souches pour le Traitement et l'Étude des Maladies Monogéniques (FR), Institut de Biologie Moléculaire et Cellulaire (FR), Université de Strasbourg (FR)
Fondation de France
Good health and well-being
Openalex Percentile: Top 2%
Down syndrome and intellectual disability research
9.39
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