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OFIP/KIAA0753 forms a complex with OFD1 and FOR20 at pericentriolar satellites and centrosomes and is mutated in one individual with oral-facial-digital syndrome

Abstract : Oral-facial-digital (OFD) syndromes are rare heterogeneous disorders characterized by the association of abnormalities of the face, the oral cavity and the extremities, some due to mutations in proteins of the transition zone of the primary cilia or the closely associated distal end of centrioles. These two structures are essential for the formation of functional cilia, and for signaling events during development. We report here causal compound heterozygous mutations of KIAA0753/OFIP in a patient with an OFD VI syndrome. We show that the KIAA0753/OFIP protein, whose sequence is conserved in ciliated species, associates with centrosome/centriole and pericentriolar satellites in human cells and forms a complex with FOR20 and OFD1. The decreased expression of any component of this ternary complex in RPE1 cells causes a defective recruitment onto centrosomes and satellites. The OFD KIAA0753/OFIP mutant loses its capacity to interact with FOR20 and OFD1, which may be the molecular basis of the defect. We also show that KIAA0753/OFIP has microtubule-stabilizing activity. OFD1 and FOR20 are known to regulate the integrity of the centriole distal end, confirming that this structural element is a target of importance for pathogenic mutations in ciliopathies.
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https://hal-univ-bourgogne.archives-ouvertes.fr/hal-01408932
Contributeur : Gad - Université de Bourgogne <>
Soumis le : lundi 5 décembre 2016 - 15:17:15
Dernière modification le : mercredi 19 août 2020 - 11:17:20

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Véronique Chevrier, Ange-Line Bruel, Teunis J. P. van Dam, Brunella Franco, Melissa Lo Scalzo, et al.. OFIP/KIAA0753 forms a complex with OFD1 and FOR20 at pericentriolar satellites and centrosomes and is mutated in one individual with oral-facial-digital syndrome. Human Molecular Genetics, Oxford University Press (OUP), 2016, 25 (3), pp.497 - 513. ⟨10.1093/hmg/ddv488⟩. ⟨hal-01408932⟩

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