Suppr超能文献

避免近亲繁殖对哈迪-温伯格平衡预期的影响:中性和选择位点的实例

Effect of inbreeding avoidance on Hardy-Weinberg expectations: examples of neutral and selected loci.

作者信息

Robertson A, Charlesworth D, Ober C

机构信息

Department of Human Genetics, The University of Chicago, Chicago, Illinois 60637, USA.

出版信息

Genet Epidemiol. 1999;17(3):165-73. doi: 10.1002/(SICI)1098-2272(1999)17:3<165::AID-GEPI2>3.0.CO;2-L.

Abstract

Although all human populations avoid close inbreeding, the effect of inbreeding avoidance on genotype proportions has not been formally considered. This paper examines the expected proportions of genotype frequencies after adjusting the Hardy-Weinberg model for close inbreeding avoidance in an inbred population. This corrected model was used to evaluate genotype distributions for HLA haplotypes and haplotypes created from three microsatellite loci on human chromosome 13 in a sample of 315 married Hutterites. In this sample, there were five individuals who were homozygous for an HLA haplotype and 15 individuals who were homozygous for a chromosome 13 haplotype. The expected numbers of homozygotes were 21 for HLA and 26 for chromosome 13 haplotypes using a model adjusted for overall inbreeding (P = 0.00031 for HLA and P = 0.019 for chromosome 13) and 18 for HLA and 22 chromosome 13 haplotypes using a model adjusted for both overall inbreeding and close inbreeding avoidance (P = 0. 0016 for HLA and P = 0.099 for chromosome 13). The model that takes into account both overall inbreeding and inbreeding avoidance provided a better fit to the observed genotype distributions for chromosome 13 haplotypes (P = 0.099), suggesting that nonrandom aspects of Hutterite mating structure, other than inbreeding and inbreeding avoidance, have small effects on genotype distributions in the population. The fact that significant deficiencies of HLA homozygotes persist after taking into account inbreeding avoidance further suggests that factors related to the HLA haplotype per se influence the genotype proportions at HLA loci in the Hutterites.

摘要

虽然所有人类群体都避免近亲繁殖,但近亲繁殖避免对基因型比例的影响尚未得到正式考量。本文研究了在一个近亲繁殖群体中,对哈迪-温伯格模型进行近亲繁殖避免调整后,基因型频率的预期比例。这个校正后的模型被用于评估315名已婚哈特派信徒样本中人类染色体13上的三个微卫星位点所产生的单倍型以及HLA单倍型的基因型分布。在这个样本中,有5个人的HLA单倍型是纯合的,15个人的染色体13单倍型是纯合的。使用针对总体近亲繁殖进行调整的模型,HLA纯合子的预期数量为21个,染色体13单倍型为26个(HLA的P值 = 0.00031,染色体13的P值 = 0.019);使用针对总体近亲繁殖和近亲繁殖避免都进行调整的模型,HLA纯合子为18个,染色体13单倍型为22个(HLA的P值 = 0.0016,染色体13的P值 = 0.099)。同时考虑总体近亲繁殖和近亲繁殖避免的模型对观察到的染色体13单倍型基因型分布拟合得更好(P值 = 0.099),这表明除了近亲繁殖和近亲繁殖避免之外,哈特派交配结构的非随机因素对群体中的基因型分布影响较小。在考虑近亲繁殖避免后,HLA纯合子仍存在显著不足这一事实进一步表明,与HLA单倍型本身相关的因素影响了哈特派中HLA位点的基因型比例。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验