• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

人类短串联重复序列多态性的进化

Short tandem repeat polymorphism evolution in humans.

作者信息

Calafell F, Shuster A, Speed W C, Kidd J R, Kidd K K

机构信息

Department of Genetics, Yale University School of Medicine, New Haven, CT 06520-8005, USA.

出版信息

Eur J Hum Genet. 1998 Jan;6(1):38-49. doi: 10.1038/sj.ejhg.5200151.

DOI:10.1038/sj.ejhg.5200151
PMID:9781013
Abstract

Forty-five dinucleotide short tandem repeat polymorphisms were typed in ten large samples of a globally distributed set of populations. Although these markers had been selected for high heterozygosity in European populations, we found them to be sufficiently informative for linkage analysis in non-Europeans. Heterozygosity, mean number of alleles, and mean number of private alleles followed a common trend: they were highest in the African samples, were somewhat lower in Europeans and East Asians, and were lowest in Amerindians. Genetic distances also reflected this pattern, and distances modelled after the stepwise mutation model yielded trees that were less in agreement with other genetic and archaeological evidence than distances based on differentiation by drift (FST). Genetic variation in non-Africans seems to be a subset of that in Africans, supporting the replacement hypothesis for the origin of modern humans.

摘要

在一组全球分布的人群的十个大样本中,对45个二核苷酸短串联重复多态性进行了分型。尽管这些标记是为在欧洲人群中具有高杂合性而选择的,但我们发现它们对非欧洲人群的连锁分析也具有足够的信息量。杂合性、等位基因平均数和私有等位基因平均数呈现出共同趋势:在非洲样本中最高,在欧洲人和东亚人中略低,在美洲印第安人中最低。遗传距离也反映了这种模式,基于逐步突变模型建模的距离所产生的树状图与其他遗传和考古证据的一致性不如基于遗传漂变分化(FST)的距离。非洲以外人群的遗传变异似乎是非洲人群遗传变异的一个子集,这支持了现代人类起源的替代假说。

相似文献

1
Short tandem repeat polymorphism evolution in humans.人类短串联重复序列多态性的进化
Eur J Hum Genet. 1998 Jan;6(1):38-49. doi: 10.1038/sj.ejhg.5200151.
2
Global survey of haplotype frequencies and linkage disequilibrium at the RET locus.RET基因座单倍型频率及连锁不平衡的全球调查。
Eur J Hum Genet. 2003 Oct;11(10):760-9. doi: 10.1038/sj.ejhg.5201036.
3
Genetic diversity and evolution of the human leptin locus tetranucleotide repeat.人类瘦素基因座四核苷酸重复序列的遗传多样性与进化
Hum Genet. 2002 May;110(5):412-7. doi: 10.1007/s00439-002-0715-5. Epub 2002 Apr 4.
4
PKLR- GBA region shows almost complete linkage disequilibrium over 70 kb in a set of worldwide populations.在一组全球人群中,PKLR - GBA区域在70千碱基对范围内显示出几乎完全的连锁不平衡。
Hum Genet. 2002 Jun;110(6):532-44. doi: 10.1007/s00439-002-0734-2. Epub 2002 May 22.
5
Comparison of 79 DNA polymorphisms tested in Australians, Japanese and Papua New Guineans with those of five other human populations.对澳大利亚人、日本人、巴布亚新几内亚人以及其他五个人类群体所检测的79个DNA多态性进行比较。
Gene Geogr. 1994 Dec;8(3):191-214.
6
Global genetic variation at nine short tandem repeat loci and implications on forensic genetics.九个短串联重复序列位点的全球遗传变异及其对法医遗传学的影响。
Eur J Hum Genet. 2003 Jan;11(1):39-49. doi: 10.1038/sj.ejhg.5200902.
7
Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins.PLAT基因座处的短串联重复多态性/Alu单倍型变异:对现代人类起源的影响。
Am J Hum Genet. 2000 Oct;67(4):901-25. doi: 10.1086/303068. Epub 2000 Sep 13.
8
[A population genetics study of the allelic polymorphism in the hypervariable region of the apolipoprotein B gene in the population of different regions of Ukraine].[乌克兰不同地区人群载脂蛋白B基因高变区等位基因多态性的群体遗传学研究]
Tsitol Genet. 1996 Sep-Oct;30(5):35-41.
9
DYS19 and DYS390 Y-STR polymorphism in the Iberian Peninsula: a multivariate analysis.伊比利亚半岛DYS19和DYS390 Y染色体短串联重复序列多态性:一项多变量分析
Anthropol Anz. 2003 Mar;61(1):49-62.
10
Linkage disequilibrium between alleles at highly polymorphic mini- and micro-satellite loci of Theileria parva isolated from cattle in three regions of Kenya.从肯尼亚三个地区的牛身上分离出的泰勒虫高度多态性微卫星和小卫星位点上等位基因之间的连锁不平衡。
Int J Parasitol. 2006 Jul;36(8):937-46. doi: 10.1016/j.ijpara.2006.01.008. Epub 2006 Mar 10.

引用本文的文献

1
Comparison of unique Dong Tao chickens from Vietnam and Thailand: genetic background and differences for resource management.越南和泰国独特的东涛鸡比较:遗传背景及资源管理差异
Genes Genomics. 2025 Apr 22. doi: 10.1007/s13258-025-01644-9.
2
SNP Genotyping Characterizes the Genome Composition of the New Baisary Fat-Tailed Sheep Breed.单核苷酸多态性基因分型表征新的拜萨里脂肪尾绵羊品种的基因组组成。
Animals (Basel). 2022 Jun 6;12(11):1468. doi: 10.3390/ani12111468.
3
Inferring biogeographic ancestry with compound markers of slow and fast evolving polymorphisms.
利用慢速和快速进化多态性的复合标记推断生物地理起源。
Eur J Hum Genet. 2018 Nov;26(11):1697-1707. doi: 10.1038/s41431-018-0215-2. Epub 2018 Jul 11.
4
β1-adrenoceptor gene Arg389Gly polymorphism and essential hypertension risk in general population: a meta-analysis.β1-肾上腺素能受体基因 Arg389Gly 多态性与一般人群原发性高血压的风险:荟萃分析。
Mol Biol Rep. 2013 Jun;40(6):4055-63. doi: 10.1007/s11033-012-2483-1. Epub 2013 Apr 16.
5
Population structure in a comprehensive genomic data set on human microsatellite variation.人类微卫星变异综合基因组数据集的种群结构。
G3 (Bethesda). 2013 May 20;3(5):891-907. doi: 10.1534/g3.113.005728.
6
Advancing genomic research and reducing health disparities: what can nurse scholars do?推进基因组学研究和减少健康差距:护理学者能做什么?
J Nurs Scholarsh. 2013 Jun;45(2):202-9. doi: 10.1111/j.1547-5069.2012.01482.x. Epub 2013 Mar 1.
7
A functional trinucleotide repeat polymorphism in the 5'-untranslated region of the glutathione biosynthetic gene GCLC is associated with increased risk for lung and aerodigestive tract cancers.谷胱甘肽生物合成基因 GCLC 5'非翻译区的功能性三核苷酸重复多态性与肺癌和呼吸道/消化道癌症风险增加相关。
Mol Carcinog. 2013 Oct;52(10):791-9. doi: 10.1002/mc.21923. Epub 2012 May 18.
8
On the size distribution of private microsatellite alleles.关于私有微卫星等位基因的大小分布
Theor Popul Biol. 2011 Sep;80(2):100-13. doi: 10.1016/j.tpb.2011.03.006. Epub 2011 Apr 15.
9
Sequence determinants of human microsatellite variability.人类微卫星变异性的序列决定因素。
BMC Genomics. 2009 Dec 16;10:612. doi: 10.1186/1471-2164-10-612.
10
Conceptualizing race in research.在研究中对种族进行概念化。
J Natl Med Assoc. 2008 Oct;100(10):1235-43. doi: 10.1016/s0027-9684(15)31470-x.