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囊性纤维化等位基因频率、性别比例异常与生育能力:突变等位基因传播的新理论

Cystic fibrosis allele frequency, sex ratio anomalies and fertility: a new theory for the dissemination of mutant alleles.

作者信息

Pritchard D J

机构信息

Division of Human Genetics, School of Pathological Sciences, Newcastle upon Tyne, UK.

出版信息

Hum Genet. 1991 Oct;87(6):671-6. doi: 10.1007/BF00201723.

Abstract

The observation that mothers of cystic fibrosis patients come from sibships that are larger than those of the fathers is explained by a decrease in sex ratio with increasing size of parental sibships. This feature also provides the basis for a new theory for the dissemination of the major mutant allele, deduced to have arisen 2,700-5,000 years ago, in accordance with an overall heterozygote advantage of around 3%. In heterozygous women with heterozygous partners, sex-related selection probably occurs after fertilization.

摘要

囊性纤维化患者的母亲来自比父亲的同胞手足更大的同胞手足群体,这一观察结果可通过随着父母同胞手足群体规模增大性别比下降来解释。这一特征也为主要突变等位基因传播的新理论提供了基础,根据约3%的总体杂合子优势推断,该突变等位基因产生于2700 - 5000年前。在杂合女性与杂合伴侣的情况下,与性别相关的选择可能在受精后发生。

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