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Am J Hum Genet. 2007 Jun;80(6):1188-93. Epub 2007 Apr 27.

Intragenic Cis and Trans modification of genetic susceptibility in DYT1 torsion dystonia.

Author information

1
Institute for Human Genetics, University of California at San Francisco, San Francisco, CA 94143, USA. rischn@humgen.ucsf.edu

Abstract

A GAG deletion in the DYT1 gene is a major cause of early-onset dystonia, but clinical disease expression occurs in only 30% of mutation carriers. To gain insight into genetic factors that may influence penetrance, we evaluated three DYT1 single-nucleotide polymorphisms, including D216H, a coding-sequence variation that moderates the effects of the DYT1 GAG deletion in cellular models. We tested DYT1 GAG-deletion carriers with (n=119) and without (n=113) clinical signs of dystonia and control individuals (n=197) and found the frequency of the 216H allele to be increased in GAG-deletion carriers without dystonia and to be decreased in carriers with dystonia, compared with the control individuals. Analysis of haplotypes demonstrated a highly protective effect of the H allele in trans with the GAG deletion; there was also suggestive evidence that the D216 allele in cis is required for the disease to be penetrant. Our findings establish, for the first time, a clinically relevant gene modifier of DYT1.

PMID:
17503336
PMCID:
PMC1867106
DOI:
10.1086/518427
[Indexed for MEDLINE]
Free PMC Article

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