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C-Nap1 mutation affects centriole cohesion and is associated with a Seckel-like syndrome in cattle

Caprine-like Generalized Hypoplasia Syndrome (SHGC) is an autosomal-recessive disorder in Montbéliarde cattle. Affected animals present a wide range of clinical features that include the following: delayed development with low birth weight, hind limb muscular hypoplasia, caprine-like thin head and p...

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Detalles Bibliográficos
Autores principales: Floriot, Sandrine, Vesque, Christine, Rodriguez, Sabrina, Bourgain-Guglielmetti, Florence, Karaiskou, Anthi, Gautier, Mathieu, Duchesne, Amandine, Barbey, Sarah, Fritz, Sébastien, Vasilescu, Alexandre, Bertaud, Maud, Moudjou, Mohammed, Halliez, Sophie, Cormier-Daire, Valérie, E.L. Hokayem, Joyce, Nigg, Erich A., Manciaux, Luc, Guatteo, Raphaël, Cesbron, Nora, Toutirais, Geraldine, Eggen, André, Schneider-Maunoury, Sylvie, Boichard, Didier, Sobczak-Thépot, Joelle, Schibler, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423223/
https://www.ncbi.nlm.nih.gov/pubmed/25902731
http://dx.doi.org/10.1038/ncomms7894
Descripción
Sumario:Caprine-like Generalized Hypoplasia Syndrome (SHGC) is an autosomal-recessive disorder in Montbéliarde cattle. Affected animals present a wide range of clinical features that include the following: delayed development with low birth weight, hind limb muscular hypoplasia, caprine-like thin head and partial coat depigmentation. Here we show that SHGC is caused by a truncating mutation in the CEP250 gene that encodes the centrosomal protein C-Nap1. This mutation results in centrosome splitting, which neither affects centriole ultrastructure and duplication in dividing cells nor centriole function in cilium assembly and mitotic spindle organization. Loss of C-Nap1-mediated centriole cohesion leads to an altered cell migration phenotype. This discovery extends the range of loci that constitute the spectrum of autosomal primary recessive microcephaly (MCPH) and Seckel-like syndromes.