| Literature DB >> 27666370 |
Elisabetta Flex1, Marcello Niceta2, Serena Cecchetti3, Isabelle Thiffault4, Margaret G Au5, Alessandro Capuano2, Emanuela Piermarini2, Anna A Ivanova6, Joshua W Francis6, Giovanni Chillemi7, Balasubramanian Chandramouli8, Giovanna Carpentieri9, Charlotte A Haaxma10, Andrea Ciolfi11, Simone Pizzi2, Ganka V Douglas12, Kara Levine12, Antonella Sferra2, Maria Lisa Dentici2, Rolph R Pfundt10, Jean-Baptiste Le Pichon13, Emily Farrow14, Frank Baas15, Fiorella Piemonte2, Bruno Dallapiccola2, John M Graham5, Carol J Saunders4, Enrico Bertini2, Richard A Kahn6, David A Koolen16, Marco Tartaglia17.
Abstract
Microtubules are dynamic cytoskeletal elements coordinating and supporting a variety of neuronal processes, including cell division, migration, polarity, intracellular trafficking, and signal transduction. Mutations in genes encoding tubulins and microtubule-associated proteins are known to cause neurodevelopmental and neurodegenerative disorders. Growing evidence suggests that altered microtubule dynamics may also underlie or contribute to neurodevelopmental disorders and neurodegeneration. We report that biallelic mutations in TBCD, encoding one of the five co-chaperones required for assembly and disassembly of the αβ-tubulin heterodimer, the structural unit of microtubules, cause a disease with neurodevelopmental and neurodegenerative features characterized by early-onset cortical atrophy, secondary hypomyelination, microcephaly, thin corpus callosum, developmental delay, intellectual disability, seizures, optic atrophy, and spastic quadriplegia. Molecular dynamics simulations predicted long-range and/or local structural perturbations associated with the disease-causing mutations. Biochemical analyses documented variably reduced levels of TBCD, indicating relative instability of mutant proteins, and defective β-tubulin binding in a subset of the tested mutants. Reduced or defective TBCD function resulted in decreased soluble α/β-tubulin levels and accelerated microtubule polymerization in fibroblasts from affected subjects, demonstrating an overall shift toward a more rapidly growing and stable microtubule population. These cells displayed an aberrant mitotic spindle with disorganized, tangle-shaped microtubules and reduced aster formation, which however did not alter appreciably the rate of cell proliferation. Our findings establish that defective TBCD function underlies a recognizable encephalopathy and drives accelerated microtubule polymerization and enhanced microtubule stability, underscoring an additional cause of altered microtubule dynamics with impact on neuronal function and survival in the developing brain.Entities:
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Year: 2016 PMID: 27666370 PMCID: PMC5065658 DOI: 10.1016/j.ajhg.2016.08.003
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025