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<dc:title xml:lang="fr">Etude du rôle de WDR47 dans le système nerveux central</dc:title>
<dcterms:alternative xml:lang="en">lnvestigating the role of WDR47 in brain function</dcterms:alternative>
<dc:subject xml:lang="fr">Gene avec des repetitions WD</dc:subject>
<dc:subject xml:lang="fr">Corps calleux</dc:subject>
<dc:subject xml:lang="fr">Microtubules</dc:subject>
<dc:subject xml:lang="fr">Cone de croissance</dc:subject>
<dc:subject xml:lang="fr">Autophagie</dc:subject>
<dc:subject xml:lang="fr">Anomalies neuro-anatomiques</dc:subject>
<dc:subject xml:lang="en">WD-repeat genes</dc:subject>
<dc:subject xml:lang="en">Corpus callosum</dc:subject>
<dc:subject xml:lang="en">Microtubules</dc:subject>
<dc:subject xml:lang="en">Growth cone</dc:subject>
<dc:subject xml:lang="en">Autophagy</dc:subject>
<dc:subject xml:lang="en">Neuroanatomical anomalies</dc:subject>
<dc:subject xsi:type="dcterms:DDC">572.8</dc:subject>
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<tef:elementdEntree autoriteExterne="031404316" autoriteSource="Sudoc">Tubulines</tef:elementdEntree>
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<tef:elementdEntree autoriteExterne="09270770X" autoriteSource="Sudoc.FMesh">Protéines à répétitions de séquences bêta-transducine</tef:elementdEntree>
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<dcterms:abstract xml:lang="fr">Nos travaux sur 26 gènes de la famille des WDR a permis d’en identifier sept (Atg16l1, Coro1c, Dmxl2, Herc1, Kif21b, Wdr47, Wdr89) associés à des anomalies cérébrales majeures. Cette grande famille de protéines reste pourtant peu explorée quant à ses rôles dans le développement du système nerveux central. Nous avons choisi d’étudier WDR47, dont la fonction est totalement inconnue en dépit d’une très grande similarité structurale avec LIS1, protéine à l’origine de la lissencéphalie. En combinant trois modèles expérimentaux (souris, siRNA et levure), nous avons démontré que Wdr47 est essentiel pour la survie de l’organisme et est impliqué dans la coordination motrice et le maintien de l’homéostasie énergétique avec une origine probablement centrale. Au niveau cellulaire, Wdr47 assure un rôle clé dans la dynamique des microtubules et la stabilisation du cône de croissance au travers d’interaction protéiques avec Reelin et SCG10. En outre, Wdr47 est aussi impliqué dans la prolifération neuronale et la macroautophagie. Ces résultats ont permis d’établir un lien de causalité entre une duplication de 200 kb contenant Wdr47 et des troubles de coordination motrice et une obésité hyperphagique chez un jeune patient.</dcterms:abstract>
<dcterms:abstract xml:lang="en">WD40-repeat (WDR) proteins are one of largest eukaryotic family, however little is known about their role in neurodevelopment. We investigated 26 WDR genes, and found 7 (Atg16l1, Coro1c, Dmxl2, Herc1, Kif21b, Wdr47, Wdr89) with a major impact in brain structure when inactivated in mice. We chose WDR47 for further investigation, as it is a completely unknown protein that shares striking domain similarity with LIS1. Using three independent model systems (mice, siRNA and yeast), we found an essential role of Wdr47 in survival, and key neuronal processes involving microtubule dynamics such as proliferation, autophagy and growth cone stabilization. Next we identified Reelin and superior cervical ganglion 10 (SCG10) as top interacting proteins of WDR47. Interestingly, a 200-kb duplication encompassing WDR47 was linked to poor coordination in one patient, recapitulating mouse behavioural anomalies. Together our data help unravel for the first time a key role of Wdr47 in brain.</dcterms:abstract>
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