Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations
Em. Valente et al., Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations, ANN HUM GEN, 63, 1999, pp. 1-8
The DYT1. gene on human chromosome 9q34 appears to be responsible for most
cases of early onset primary torsion dystonia (PTD) both in Ashkenazi Jewis
h (AJ) and in non-Jewish patients. Previous haplotype analysis in a 2 cM re
gion surrounding the DYT1 gene showed that a single founder mutation (DYT1(
AJ)) was responsible for most cases of early onset PTD in the North America
n AJ population and refined the most likely location of the gene to a 150 k
b interval between the marker loci D9S2161 and D9S63.
Recently, the majority of cases of early onset PTD in both AJ and non-Jewis
h patients were found to carry a unique 3-bp (GAG) deletion in the coding r
egion of the DYT1 gene. This deletion appears to have arisen more than once
, suggesting independent mutational events.
In this study, we analysed the haplotypes surrounding DYT1. in 9 AJ and 15
non-Jewish British patients carrying the GAG deletion in the DYT1. gene. We
found that all AJ British patients carried the same haplotype as the North
American Jews, sustaining the theory that the current British AJ community
descends from the same small group of individuals as the North American Je
wry. Furthermore, in the non-Jewish British patients, only a limited number
of distinct founder mutations was observed. This supports the hypothesis t
hat the GAG deletion in the DYT1 gene is not a very frequent mutation, and
that it has arisen only a limited number of times throughout the centuries.