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通过Y染色体DNA分析揭示的亚洲人和北欧人的遗传关系。

Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis.

作者信息

Zerjal T, Dashnyam B, Pandya A, Kayser M, Roewer L, Santos F R, Schiefenhövel W, Fretwell N, Jobling M A, Harihara S, Shimizu K, Semjidmaa D, Sajantila A, Salo P, Crawford M H, Ginter E K, Evgrafov O V, Tyler-Smith C

机构信息

Department of Biochemistry, University of Oxford, United Kingdom.

出版信息

Am J Hum Genet. 1997 May;60(5):1174-83.

PMID:9150165
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1712423/
Abstract

We have identified a new T-->C transition on the human Y chromosome. C-allele chromosomes have been found only in a subset of the populations from Asia and northern Europe and reach their highest frequencies in Yakut, Buryats, and Finns. Examination of the microsatellite haplotypes of the C-allele chromosomes suggests that the mutation occurred recently in Asia. The Y chromosome thus provides both information about population relationships in Asia and evidence for a substantial paternal genetic contribution of Asians to northern European populations such as the Finns.

摘要

我们在人类Y染色体上发现了一个新的T→C转换。仅在亚洲和北欧部分人群中发现了C等位基因染色体,在雅库特人、布里亚特人和芬兰人中其频率最高。对C等位基因染色体微卫星单倍型的检测表明,该突变最近发生在亚洲。因此,Y染色体既提供了有关亚洲人群关系的信息,也为亚洲人对芬兰等北欧人群有大量父系基因贡献提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2d4/1712423/8a81a3b127dd/ajhg00005-0174-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2d4/1712423/864c1c914b27/ajhg00005-0173-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2d4/1712423/e880cb8b9abd/ajhg00005-0174-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2d4/1712423/8a81a3b127dd/ajhg00005-0174-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2d4/1712423/864c1c914b27/ajhg00005-0173-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2d4/1712423/e880cb8b9abd/ajhg00005-0174-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2d4/1712423/8a81a3b127dd/ajhg00005-0174-b.jpg

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2
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Hum Mol Genet. 1996 Nov;5(11):1759-66. doi: 10.1093/hmg/5.11.1759.
3
Statistical properties of the variation at linked microsatellite loci: implications for the history of human Y chromosomes.连锁微卫星位点变异的统计特性:对人类Y染色体历史的启示
哥伦比亚 QM3 土著人群中的新 Y-SNPs。
PLoS One. 2023 Dec 6;18(12):e0294516. doi: 10.1371/journal.pone.0294516. eCollection 2023.
4
A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans.一种常见的 1.6mb Y 染色体倒位可导致随后的缺失和人类严重的精子发生失败。
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