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1.
Nat Genet ; 49(4): 606-612, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-28250456

RESUMO

Motor, sensory, and integrative activities of the brain are coordinated by a series of midline-bridging neuronal commissures whose development is tightly regulated. Here we report a new human syndrome in which these commissures are widely disrupted, thus causing clinical manifestations of horizontal gaze palsy, scoliosis, and intellectual disability. Affected individuals were found to possess biallelic loss-of-function mutations in the gene encoding the axon-guidance receptor 'deleted in colorectal carcinoma' (DCC), which has been implicated in congenital mirror movements when it is mutated in the heterozygous state but whose biallelic loss-of-function human phenotype has not been reported. Structural MRI and diffusion tractography demonstrated broad disorganization of white-matter tracts throughout the human central nervous system (CNS), including loss of all commissural tracts at multiple levels of the neuraxis. Combined with data from animal models, these findings show that DCC is a master regulator of midline crossing and development of white-matter projections throughout the human CNS.


Assuntos
Encéfalo/anormalidades , Neoplasias Colorretais/genética , Regulação da Expressão Gênica no Desenvolvimento/genética , Perda de Heterozigosidade/genética , Mutação/genética , Sistema Nervoso Central/anormalidades , Feminino , Humanos , Deficiência Intelectual/genética , Masculino , Neurônios/metabolismo , Fenótipo , Polimorfismo de Nucleotídeo Único/genética , Receptores de Superfície Celular/genética
2.
Hum Mol Genet ; 21(26): 5484-99, 2012 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-23001566

RESUMO

Microtubules are essential components of axon guidance machinery. Among ß-tubulin mutations, only those in TUBB3 have been shown to cause primary errors in axon guidance. All identified mutations in TUBB2B result in polymicrogyria, but it remains unclear whether TUBB2B mutations can cause axon dysinnervation as a primary phenotype. We have identified a novel inherited heterozygous missense mutation in TUBB2B that results in an E421K amino acid substitution in a family who segregates congenital fibrosis of the extraocular muscles (CFEOM) with polymicrogyria. Diffusion tensor imaging of brains of affected family members reveals aberrations in the trajectories of commissural projection neurons, implying a paucity of homotopic connections. These observations led us to ask whether axon dysinnervation is a primary phenotype, and why the E421K, but not other, TUBB2B substitutions cause CFEOM. Expression of exogenous Tubb2b-E421K in developing callosal projection neurons is sufficient to perturb homotopic connectivity, without affecting neuronal production or migration. Using in vitro biochemical assays and yeast genetics, we find that TUBB2B-E421K αß-heterodimers are incorporated into the microtubule network where they alter microtubule dynamics and can reduce kinesin localization. These data provide evidence that TUBB2B mutations can cause primary axon dysinnervation. Interestingly, by incorporating into microtubules and altering their dynamic properties, the E421K substitution behaves differently than previously identified TUBB2B substitutions, providing mechanistic insight into the divergence between resulting phenotypes. Together with previous studies, these findings highlight that ß-tubulin isotypes function in both conserved and divergent ways to support proper human nervous system development.


Assuntos
Cinesinas/metabolismo , Malformações do Desenvolvimento Cortical/genética , Músculos Oculomotores/patologia , Tubulina (Proteína)/genética , Alelos , Substituição de Aminoácidos/genética , Axônios/metabolismo , Encéfalo/anormalidades , Encéfalo/metabolismo , Feminino , Fibrose , Heterozigoto , Humanos , Cinesinas/genética , Masculino , Malformações do Desenvolvimento Cortical/patologia , Microtúbulos/genética , Microtúbulos/metabolismo , Mutação de Sentido Incorreto , Neurogênese , Neurônios/metabolismo , Neurônios/fisiologia , Linhagem , Fenótipo , Ligação Proteica , Tubulina (Proteína)/metabolismo
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