Authors:
CM Ambrose, MP Duyao, G Barnes, GP Bates, CS Lin, J Srinidhi, S Baxendale, H Hummerich, H Lehrach, M Altherr, J Wasmuth, A Buckler, D Church, D Housman, M Berks, G Micklem, R Durbin, A Dodge, A Read, J Gusella, ME MacDonald
Journal name: 
Somat Cell Mol Genet
Citation info: 
20(1):27-38
Abstract: 
Huntington's disease, a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expanded, unstable trinucleotide repeat in a novel 4p16.3 gene. To lay the foundation for exploring the pathogenic mechanism in HD, we have determined the structure of the disease gene and examined its expression. The HD locus spans 180 kb and consists of 67 exons ranging in size from 48 bp to 341 bp with an average of 138 bp. Scanning of the HD transcript failed to reveal any additional sequence alterations characteristic of HD chromosomes. A codon loss polymorphism in linkage disequilibrium with the disorder revealed that both normal and HD alleles are represented in the mRNA population in HD heterozygotes, indicating that the defect does not eliminate transcription. The gene is ubiquitously expressed as two alternatively polyadenylated forms displaying different relative abundance in various fetal and adult tissues, suggesting the operation of interacting factors in determining specificity of cell loss. The HD gene was disrupted in a female carrying a balanced translocation with a breakpoint between exons 40 and 41. The absence of any abnormal phenotype in this individual argues against simple inactivation of the gene as the mechanism by which the expanded trinucleotide repeat causes HD. Taken together, these observations suggest that the dominant HD mutation either confers a new property on the mRNA or, more likely, alters an interaction at the protein level.
DOI: 
http://doi.org/10.1007/BF02257483
E-pub date: 
01 Jan 1994
Users with this publication listed: 
Gos Micklem