Skip to Main content Skip to Navigation
Journal articles

Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity

Laure Asselin 1 José Rivera Alvarez 1 Solveig Heide 2, 3, 4 Camille Bonnet 1 Peggy Tilly 1 Hélène Vitet 5, 6 Chantal Weber 1 Carlos Bacino 7, 8 Kristin Baranaño 9 Anna Chassevent 9 Amy Dameron 10 Laurence Faivre 11, 12, 13, 14 Neil Hanchard 7 Sonal Mahida 15 Kirsty Mcwalter 10 Cyril Mignot 2, 3, 4, 16 Caroline Nava 2, 16 Agnès Rastetter 16 Haley Streff 7, 8 Christel Thauvin-Robinet 11, 12, 13, 4 Marjan Weiss 17 Gladys Zapata 8 Petra Zwijnenburg 17 Frédéric Saudou 5 Christel Depienne 1, 16, 18 Christelle Golzio 1 Delphine Héron 2, 3, 4 Juliette Godin 1 
Abstract : Abstract KIF21B is a kinesin protein that promotes intracellular transport and controls microtubule dynamics. We report three missense variants and one duplication in KIF21B in individuals with neurodevelopmental disorders associated with brain malformations, including corpus callosum agenesis (ACC) and microcephaly. We demonstrate, in vivo, that the expression of KIF21B missense variants specifically recapitulates patients’ neurodevelopmental abnormalities, including microcephaly and reduced intra- and inter-hemispheric connectivity. We establish that missense KIF21B variants impede neuronal migration through attenuation of kinesin autoinhibition leading to aberrant KIF21B motility activity. We also show that the ACC-related KIF21B variant independently perturbs axonal growth and ipsilateral axon branching through two distinct mechanisms, both leading to deregulation of canonical kinesin motor activity. The duplication introduces a premature termination codon leading to nonsense-mediated mRNA decay. Although we demonstrate that Kif21b haploinsufficiency leads to an impaired neuronal positioning, the duplication variant might not be pathogenic. Altogether, our data indicate that impaired KIF21B autoregulation and function play a critical role in the pathogenicity of human neurodevelopmental disorder.
Complete list of metadata
Contributor : Juliette Godin Connect in order to contact the contributor
Submitted on : Monday, October 11, 2021 - 4:43:29 PM
Last modification on : Thursday, August 4, 2022 - 5:22:19 PM

Links full text



Laure Asselin, José Rivera Alvarez, Solveig Heide, Camille Bonnet, Peggy Tilly, et al.. Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity. Nature Communications, Nature Publishing Group, 2020, 11 (1), ⟨10.1038/s41467-020-16294-6⟩. ⟨hal-03373809⟩



Record views