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Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features
Valter Tucci, … , Sara Wells, Patrick M. Nolan
Valter Tucci, … , Sara Wells, Patrick M. Nolan
Published March 10, 2014
Citation Information: J Clin Invest. 2014;124(4):1468-1482. https://doi.org/10.1172/JCI70372.
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Research Article Neuroscience

Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features

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Abstract

The recent identification of multiple dominant mutations in the gene encoding β-catenin in both humans and mice has enabled exploration of the molecular and cellular basis of β-catenin function in cognitive impairment. In humans, β-catenin mutations that cause a spectrum of neurodevelopmental disorders have been identified. We identified de novo β-catenin mutations in patients with intellectual disability, carefully characterized their phenotypes, and were able to define a recognizable intellectual disability syndrome. In parallel, characterization of a chemically mutagenized mouse line that displays features similar to those of human patients with β-catenin mutations enabled us to investigate the consequences of β-catenin dysfunction through development and into adulthood. The mouse mutant, designated batface (Bfc), carries a Thr653Lys substitution in the C-terminal armadillo repeat of β-catenin and displayed a reduced affinity for membrane-associated cadherins. In association with this decreased cadherin interaction, we found that the mutation results in decreased intrahemispheric connections, with deficits in dendritic branching, long-term potentiation, and cognitive function. Our study provides in vivo evidence that dominant mutations in β-catenin underlie losses in its adhesion-related functions, which leads to severe consequences, including intellectual disability, childhood hypotonia, progressive spasticity of lower limbs, and abnormal craniofacial features in adults.

Authors

Valter Tucci, Tjitske Kleefstra, Andrea Hardy, Ines Heise, Silvia Maggi, Marjolein H. Willemsen, Helen Hilton, Chris Esapa, Michelle Simon, Maria-Teresa Buenavista, Liam J. McGuffin, Lucie Vizor, Luca Dodero, Sotirios Tsaftaris, Rosario Romero, Willy N. Nillesen, Lisenka E.L.M. Vissers, Marlies J. Kempers, Anneke T. Vulto-van Silfhout, Zafar Iqbal, Marta Orlando, Alessandro Maccione, Glenda Lassi, Pasqualina Farisello, Andrea Contestabile, Federico Tinarelli, Thierry Nieus, Andrea Raimondi, Barbara Greco, Daniela Cantatore, Laura Gasparini, Luca Berdondini, Angelo Bifone, Alessandro Gozzi, Sara Wells, Patrick M. Nolan

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Figure 3

MRI scans of Bfc/+ mice reveal major brain abnormalities.

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MRI scans of Bfc/+ mice reveal major brain abnormalities.
 
MRI scans of...
MRI scans of Bfc/+ mice highlighted an altered cranial shape with a larger left-right axis and a shorter longitudinal extension compared with controls. The effect was apparent in horizontal (A) and sagital (B) views of the brain. The olfactory bulbs and cerebellum appeared to be significantly smaller in Bfc/+ individuals compared with control littermates. In 3 out of 10 Bfc/+ subjects, the corpus callosum appeared to be severely underdeveloped, lacking any interhemispheric extension. This was apparent in anatomical T2-weighted images (C) as well as in diffusion-weighted scans (D and E). Diffusion tensor images (DTI) modulated by FA (D) and DTI tractography corroborated the lack of interhemispheric connection of the corpus callosum in all of the 3 subjects, showing abnormal callosal anatomy in anatomical MRI images (C, D, and E show data from representative Bfc/+ and control subjects). Normal interhemispheric tracts were observed in all the control subject images. Cereb, cerebellum; Cpu, caudate putamen; Olf Bulb, olfactory bulbs; Hippoc, hippocampus; Hypot, hypothalamus.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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