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两个犹太人群体中的线粒体DNA多态性

mtDNA polymorphism in two communities of Jews.

作者信息

Tikochinski Y, Ritte U, Gross S R, Prager E M, Wilson A C

机构信息

Department of Genetics, Hebrew University, Jerusalem.

出版信息

Am J Hum Genet. 1991 Jan;48(1):129-36.

PMID:1670749
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1682746/
Abstract

Twenty-one types of mtDNA were found in a survey of 39 Israeli Jews, of whom 18 were Sephardic and 21 Ashkenazic. The survey was made with six restriction enzymes that together recognize an average of 600 bp/genome. The differences among the types appear to be due to base substitution at 19 cleavage sites, one deletion, and one conformational mutation. The numbers of differences imply that these modern Jews stem from a minimum of 21 maternal lineages that were already distinct from one another 4,000-5,000 years ago. In three of the four cases where a type was found in more than one person, it occurred in both Ashkenazic and Sephardic populations. The diversity of types in the combined sample of two Jewish populations is lower than both that in a sample from various parts of Africa and that in a sample from various parts of East Asia. Nevertheless, it is as high as that in a sample from diverse parts of New Guinea, an area much larger than that in Israel to which the Jewish population traces back.

摘要

在对39名以色列犹太人的调查中发现了21种线粒体DNA(mtDNA)类型,其中18名是西班牙系犹太人,21名是阿什肯纳兹系犹太人。该调查使用了六种限制酶,这些酶共同识别的平均长度为每个基因组600个碱基对。这些类型之间的差异似乎是由于19个切割位点的碱基替换、一个缺失和一个构象突变造成的。差异的数量表明,这些现代犹太人至少起源于21个母系血统,这些血统在4000至5000年前就已经彼此不同。在四种类型被不止一人发现的情况中,有三种情况同时出现在阿什肯纳兹系和西班牙系人群中。两个犹太人群体的组合样本中的类型多样性低于来自非洲各地的样本和来自东亚各地的样本。然而,它与来自新几内亚不同地区的样本一样高,新几内亚的面积比犹太人群体追溯的以色列地区大得多。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc97/1682746/eb2fad6cc174/ajhg00085-0135-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc97/1682746/eb2fad6cc174/ajhg00085-0135-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc97/1682746/eb2fad6cc174/ajhg00085-0135-a.jpg

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Genomewide linkage scan for bipolar-disorder susceptibility loci among Ashkenazi Jewish families.对阿什肯纳兹犹太家庭中双相情感障碍易感基因座进行全基因组连锁扫描。

本文引用的文献

1
Sequence and organization of the human mitochondrial genome.人类线粒体基因组的序列与组织
Nature. 1981 Apr 9;290(5806):457-65. doi: 10.1038/290457a0.
2
Polymorphic sites and the mechanism of evolution in human mitochondrial DNA.人类线粒体DNA中的多态性位点与进化机制。
Genetics. 1984 Mar;106(3):479-99. doi: 10.1093/genetics/106.3.479.
3
Length mutations in human mitochondrial DNA.人类线粒体DNA中的长度突变。
Am J Hum Genet. 2004 Aug;75(2):204-19. doi: 10.1086/422474. Epub 2004 Jun 18.
4
Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.对德系犹太人家族中精神分裂症易感基因座进行全基因组连锁扫描,结果显示10号染色体q22区域存在连锁证据。
Am J Hum Genet. 2003 Sep;73(3):601-11. doi: 10.1086/378158. Epub 2003 Aug 15.
5
Founding mothers of Jewish communities: geographically separated Jewish groups were independently founded by very few female ancestors.犹太社区的开国之母:地理上相互隔离的犹太群体是由极少数女性祖先独立创建的。
Am J Hum Genet. 2002 Jun;70(6):1411-20. doi: 10.1086/340609. Epub 2002 Apr 30.
6
Distinctive genetic signatures in the Libyan Jews.利比亚犹太人独特的基因特征。
Proc Natl Acad Sci U S A. 2001 Jan 30;98(3):858-63. doi: 10.1073/pnas.98.3.858.
7
Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes.犹太人群体和中东非犹太人群体共享一组常见的Y染色体双等位基因单倍型。
Proc Natl Acad Sci U S A. 2000 Jun 6;97(12):6769-74. doi: 10.1073/pnas.100115997.
8
mtDNA analysis of Nile River Valley populations: A genetic corridor or a barrier to migration?尼罗河流域人群的线粒体DNA分析:是基因走廊还是迁徙障碍?
Am J Hum Genet. 1999 Apr;64(4):1166-76. doi: 10.1086/302314.
9
Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype.突尼斯裔犹太人易患脆性X综合征是由于一种罕见的地中海单倍型上不存在AGG中断。
Am J Hum Genet. 1997 Jan;60(1):103-12.
10
The sequence of human mtDNA: the question of errors versus polymorphisms.人类线粒体DNA序列:错误与多态性问题
Am J Hum Genet. 1992 Jun;50(6):1333-40.
Genetics. 1983 Aug;104(4):699-711. doi: 10.1093/genetics/104.4.699.
4
Radiation of human mitochondria DNA types analyzed by restriction endonuclease cleavage patterns.通过限制性内切酶切割模式分析人类线粒体DNA类型的辐射。
J Mol Evol. 1983;19(3-4):255-71. doi: 10.1007/BF02099973.
5
Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA.人类线粒体DNA Hpa 1核酸内切酶切割模式的种族差异。
Proc Natl Acad Sci U S A. 1981 Sep;78(9):5768-72. doi: 10.1073/pnas.78.9.5768.
6
DNA polymorphism detectable by restriction endonucleases.可通过限制性核酸内切酶检测到的DNA多态性。
Genetics. 1981 Jan;97(1):145-63. doi: 10.1093/genetics/97.1.145.
7
Polymorphism in mitochondrial DNA of humans as revealed by restriction endonuclease analysis.通过限制性内切酶分析揭示的人类线粒体DNA多态性。
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3605-9. doi: 10.1073/pnas.77.6.3605.
8
Rate of sequence divergence estimated from restriction maps of mitochondrial DNAs from Papua New Guinea.根据巴布亚新几内亚线粒体DNA限制酶切图谱估算的序列分歧率。
Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:433-9. doi: 10.1101/sqb.1986.051.01.052.
9
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.与莱伯遗传性视神经病变相关的线粒体DNA突变。
Science. 1988 Dec 9;242(4884):1427-30. doi: 10.1126/science.3201231.
10
Mitochondrial DNA sequences from a 7000-year old brain.来自一个7000年前大脑的线粒体DNA序列。
Nucleic Acids Res. 1988 Oct 25;16(20):9775-87. doi: 10.1093/nar/16.20.9775.