Risch N, de Leon D, Ozelius L, Kramer P, Almasy L, Singer B, Fahn S, Breakefield X, Bressman S
Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Nat Genet. 1995 Feb;9(2):152-9. doi: 10.1038/ng0295-152.
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.
我们研究了来自59个患有特发性扭转性肌张力障碍(ITD)的阿什肯纳兹犹太家庭的9号染色体q34区域六个紧密连锁的微卫星位点的数据。我们的数据表明,阿什肯纳兹人群中绝大多数(>90%)早发性ITD病例是由一个单一的奠基者突变引起的,我们估计该突变大约在350年前首次出现。我们还表明,携带者优先来自历史上犹太聚居区的北部(立陶宛和白俄罗斯)。这种显性突变的近期起源及其当前的高频率(在1/6000至1/2000之间)表明,阿什肯纳兹人群起源于有限的一群奠基者,并强调了基因漂变在决定该人群疾病等位基因频率方面的重要性。