Characterization of novel dystonia musculorum mutant mice: Implications for central nervous system abnormality

Abstract We identified a novel spontaneous mutant mouse showing motor symptoms that are similar to those of the dystonia musculorum ( dt ) mouse . The observations suggested that the mutant mice inherited the mild dt phenotype as an autosomal recessive trait. Linkage analysis showed that the causative gene was located near D1Mit373 and D1Mit410 microsatellite markers on chromosome 1, which are close to the dystonin ( Dst ) gene locus. To investigate whether Dst is the causative gene of the novel mutant phenotype, we crossed the mutant with Dst gene trap ( Dst Gt ) mice. Compound heterozygotes showed a typical dt phenotype with sensory degeneration and progressive motor symptoms. DNA sequencing analysis identified a nonsense mutation within the spectrin repeats of the plakin domain. The novel mutant allele was named dt 23Rbrc . Motor abnormalities in homozygous dt 23Rbrc /dt 23Rbrc mice are not as severe as homozygous Dst Gt /Dst Gt mice. Histological analyses showed abnormal neurofilament (NF) accumulation in the nervous system of homozygous dt 23Rbrc /dt 23Rbrc mice, which is characteristic of the dt phenotype. We mapped the distribution of abnormal NF-accumulated neurons in the brain and found that they were located specifically in the brainstem, spinal cord, and in regions such as the vestibular nucleus, reticular nucleus, and red nucleus, which are implicated in posture and motor coordination pathways. The quantification of abnormal NF accumulation in the cytoplasm and spheroids (axons) of neurons showed that abnormal NF immunoreactivity was lower in homozygous dt 23Rbrc / dt 23Rbrc mice than in homozygous Dst Gt / Dst Gt mice. Therefore, we have identified a novel hypomorphic allele of dt , which causes histological abnormalities in the central nervous system that may account for the abnormal motor phenotype. This novel spontaneously occurring mutant may become a good model of hereditary sensory and autonomic neuropathy type 6, which is caused by mutations in the human DST gene.