GENETIC-ANALYSIS OF IDIOPATHIC TORSION DYSTONIA IN ASHKENAZI JEWS AND THEIR RECENT DESCENT FROM A SMALL FOUNDER POPULATION

被引:349
作者
RISCH, N
DELEON, D
OZELIUS, L
KRAMER, P
ALMASY, L
SINGER, B
FAHN, S
BREAKEFIELD, X
BRESSMAN, S
机构
[1] YALE UNIV,SCH MED,DEPT EPIDEMIOL & PUBL HLTH,NEW HAVEN,CT 06520
[2] YALE UNIV,SCH MED,DEPT GENET,NEW HAVEN,CT 06520
[3] COLUMBIA PRESBYTERIAN MED CTR,INST NEUROL,DYSTONIA CLIN RES CTR,NEW YORK,NY 10032
[4] MASSACHUSETTS GEN HOSP E,NEUROSCI CTR NEUROL,MOLEC NEUROGENET UNIT,BOSTON,MA 02129
[5] HARVARD UNIV,SCH MED,DEPT GENET,BOSTON,MA 02115
[6] OREGON HLTH SCI UNIV,DEPT NEUROL,PORTLAND,OR 97201
[7] HARVARD UNIV,SCH MED,PROGRAM NEUROSCI,BOSTON,MA 02115
[8] PRINCETON UNIV,OFF POPULAT RES,PRINCETON,NJ 08544
关键词
D O I
10.1038/ng0295-152
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have examined data on six closely linked microsatellite loci on chromosome 9q34 from 59 Ashkenazi Jewish families with idiopathic torsion dystonia (ITD). Our data show that the vast majority (>90%) of early-onset ITD cases in the Ashkenazi population are due to a single founder mutation, which we estimate first appeared approximately 350 years ago. We also show that carriers preferentially originate from the northern part of the historic Jewish Pale of settlement (Lithuania and Byelorussia). The recent origin of this dominant mutation and its current high frequency (between 1/6,000 and 1/2,000) suggest that the Ashkenazi population descends from a limited group of founders, and emphasize the importance of genetic drift in determining disease allele frequencies in this population.
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页码:152 / 159
页数:8
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