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本文引用的文献

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Microsatellite diversity and the demographic history of modern humans.微卫星多样性与现代人类的人口历史。
Proc Natl Acad Sci U S A. 1997 Apr 1;94(7):3100-3. doi: 10.1073/pnas.94.7.3100.
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Relative mutation rates at di-, tri-, and tetranucleotide microsatellite loci.二核苷酸、三核苷酸和四核苷酸微卫星位点的相对突变率。
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Dynamics of repeat polymorphisms under a forward-backward mutation model: within- and between-population variability at microsatellite loci.前向-后向突变模型下重复多态性的动态:微卫星位点的群体内和群体间变异性
Genetics. 1996 May;143(1):549-55. doi: 10.1093/genetics/143.1.549.
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A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.一项针对人类非胰岛素依赖型(2型)糖尿病基因的全基因组搜索在2号染色体上发现了一个主要的易感位点。
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Mutation of human short tandem repeats.人类短串联重复序列的突变
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微卫星重复数据中的种群扩张特征。

Signatures of population expansion in microsatellite repeat data.

作者信息

Kimmel M, Chakraborty R, King J P, Bamshad M, Watkins W S, Jorde L B

机构信息

Department of Statistics, Rice University, Houston, Texas 77251, USA.

出版信息

Genetics. 1998 Apr;148(4):1921-30. doi: 10.1093/genetics/148.4.1921.

DOI:10.1093/genetics/148.4.1921
PMID:9560405
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1460085/
Abstract

To examine the signature of population expansion on genetic variability at microsatellite loci, we consider a population that evolves according to the time-continuous Moran model, with growing population size and mutations that follow a general asymmetric stepwise mutation model. We present calculations of expected allele-size variance and homozygosity at a locus in such a model for several variants of growth, including stepwise, exponential, and logistic growth. These calculations in particular prove that population bottleneck followed by growth in size causes an imbalance between allele size variance and heterozygosity, characterized by the variance being transiently higher than expected under equilibrium conditions. This effect is, in a sense, analogous to that demonstrated before for the infinite allele model, where the number of alleles transiently increases after a stepwise growth of population. We analyze a set of data on tetranucleotide repeats that reveals the imbalance expected under the assumption of bottleneck followed by population growth in two out of three major racial groups. The imbalance is strongest in Asians, intermediate in Europeans, and absent in Africans. This finding is consistent with previous findings by others concerning the population expansion of modern humans, with the bottleneck event being most ancient in Africans, most recent in Asians, and intermediate in Europeans. Nevertheless, the imbalance index alone cannot reliably estimate the time of initiation of population expansion.

摘要

为了研究微卫星位点上群体扩张对遗传变异性的特征,我们考虑一个根据时间连续的莫兰模型进化的群体,其群体规模不断增长,且突变遵循一般的不对称逐步突变模型。我们给出了在这样一个模型中,针对包括逐步增长、指数增长和逻辑斯蒂增长等几种增长变体,一个位点上预期等位基因大小方差和纯合度的计算。这些计算特别证明,群体瓶颈后接着规模增长会导致等位基因大小方差和杂合度之间的失衡,其特征是该方差在平衡条件下暂时高于预期。从某种意义上说,这种效应类似于之前在无限等位基因模型中所证明的效应,即在群体逐步增长后等位基因数量会暂时增加。我们分析了一组关于四核苷酸重复序列的数据,该数据揭示了在三个主要种族群体中的两个群体中,在经历瓶颈后接着群体增长的假设下预期的失衡情况。这种失衡在亚洲人中最强,在欧洲人中居中,在非洲人中不存在。这一发现与其他人之前关于现代人类群体扩张的发现一致,瓶颈事件在非洲人中最为古老,在亚洲人中最为近期,在欧洲人中居中。然而,仅失衡指数不能可靠地估计群体扩张开始的时间。