Title

An active dominant mutation of glycyl-tRNA synthetase causes neuropathy in a Charcot-Marie-Tooth 2D mouse model.

Document Type

Article

Publication Date

2006

Keywords

Animals, Axons, Base-Sequence, Charcot-Marie-Tooth-Disease, Chromosome-Mapping, Disease-Models-Animal, Female, Genes-Dominant, Glycine-tRNA-Ligase, Humans, Male, Mice-Inbred-BALB-C, Mice-Inbred-C57BL, Microscopy-Electron-Transmission, Molecular-Sequence-Data, Mutation, Neuromuscular-Junction, Peripheral-Nervous-System-Diseases, Sciatic-Nerve, Sequence-Homology-Amino-Acid

JAX Source

Neuron 2006 Sep; 51(6):715-26.

Abstract

Of the many inherited Charcot-Marie-Tooth peripheral neuropathies, type 2D (CMT2D) is caused by dominant point mutations in the gene GARS, encoding glycyl tRNA synthetase (GlyRS). Here we report a dominant mutation in Gars that causes neuropathy in the mouse. Importantly, both sensory and motor axons are affected, and the dominant phenotype is not caused by a loss of the GlyRS aminoacylation function. Mutant mice have abnormal neuromuscular junction morphology and impaired transmission, reduced nerve conduction velocities, and a loss of large-diameter peripheral axons, without defects in myelination. The mutant GlyRS enzyme retains aminoacylation activity, and a loss-of-function allele, generated by a gene-trap insertion, shows no dominant phenotype in mice. These results indicate that the CMT2D phenotype is caused not by reduction of the canonical GlyRS activity and insufficiencies in protein synthesis, but instead by novel pathogenic roles for the mutant GlyRS that specifically affect peripheral neurons.