Greater Baltimore Medical Center Baltimore

Point of Rocks, MD, United States

Greater Baltimore Medical Center Baltimore

Point of Rocks, MD, United States
SEARCH FILTERS
Time filter
Source Type

Tischfield M.A.,Childrens Hospital Boston | Tischfield M.A.,Harvard University | Baris H.N.,Childrens Hospital Boston | Wu C.,Childrens Hospital Boston | And 63 more authors.
Cell | Year: 2010

We report that eight heterozygous missense mutations in TUBB3, encoding the neuron-specific β-tubulin isotype III, result in a spectrum of human nervous system disorders that we now call the TUBB3 syndromes. Each mutation causes the ocular motility disorder CFEOM3, whereas some also result in intellectual and behavioral impairments, facial paralysis, and/or later-onset axonal sensorimotor polyneuropathy. Neuroimaging reveals a spectrum of abnormalities including hypoplasia of oculomotor nerves and dysgenesis of the corpus callosum, anterior commissure, and corticospinal tracts. A knock-in disease mouse model reveals axon guidance defects without evidence of cortical cell migration abnormalities. We show that the disease-associated mutations can impair tubulin heterodimer formation in vitro, although folded mutant heterodimers can still polymerize into microtubules. Modeling each mutation in yeast tubulin demonstrates that all alter dynamic instability whereas a subset disrupts the interaction of microtubules with kinesin motors. These findings demonstrate that normal TUBB3 is required for axon guidance and maintenance in mammals. © 2010 Elsevier Inc. All rights reserved.

Loading Greater Baltimore Medical Center Baltimore collaborators
Loading Greater Baltimore Medical Center Baltimore collaborators