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在患有泰-萨克斯病的携带者中,戈谢病携带者的比例较低。

Lower frequency of Gaucher disease carriers among Tay-Sachs disease carriers.

作者信息

Peleg L, Frisch A, Goldman B, Karpaty M, Narinsky R, Bronstein S, Frydman M

机构信息

Genetic Institute, Sheba Medical Center, Tel Hashomer, Israel.

出版信息

Eur J Hum Genet. 1998 Mar-Apr;6(2):185-6. doi: 10.1038/sj.ejhg.5200176.

Abstract

The heterozygote frequency of Gaucher disease (GD) and Tay-Sachs disease (TSD) is distinctly high among Ashkenazi Jews (1:29 for TSD and 1:16 for GD). Two main theories have been suggested to explain this high occurrence: a founder effect with subsequent genetic drift, and a selective advantage of heterozygotes. We compared the frequency of the GD most common mutation (1226A-->G) among carriers of the common TSD mutation (+1277 TATC) with the frequency of this mutation in the general Ashkenazi population. The frequency of GD carriers among 308 TSD heterozygotes was 1:28 which is about half the expected (P = 0.03). These results indicate that carriers of both diseases do not possess additional evolutionary advantage over single mutation carriers. A reasonable interpretation of these findings is that one or both mutations have arisen relatively recently in different regions of Europe and have not yet reached genetic equilibrium.

摘要

在德系犹太人中,戈谢病(GD)和泰-萨克斯病(TSD)的杂合子频率明显较高(TSD为1:29,GD为1:16)。关于这种高发病率,人们提出了两种主要理论:一是奠基者效应及随后的遗传漂变,二是杂合子的选择优势。我们将常见TSD突变(+1277 TATC)携带者中GD最常见突变(1226A→G)的频率与德系犹太普通人群中该突变的频率进行了比较。在308名TSD杂合子中,GD携带者的频率为1:28,约为预期频率的一半(P = 0.03)。这些结果表明,这两种疾病的携带者并不比单突变携带者具有额外的进化优势。对这些发现的一个合理的解释是,这两种突变中的一种或两种是最近在欧洲不同地区出现的,尚未达到遗传平衡。

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