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本文引用的文献

1
Evolutionary toggling of the MAPT 17q21.31 inversion region.微管相关蛋白tau基因(MAPT)17q21.31倒位区域的进化切换
Nat Genet. 2008 Sep;40(9):1076-83. doi: 10.1038/ng.193.
2
Worldwide human relationships inferred from genome-wide patterns of variation.从全基因组变异模式推断全球人类关系。
Science. 2008 Feb 22;319(5866):1100-4. doi: 10.1126/science.1153717.
3
Genotype, haplotype and copy-number variation in worldwide human populations.全球人类群体中的基因型、单倍型和拷贝数变异。
Nature. 2008 Feb 21;451(7181):998-1003. doi: 10.1038/nature06742.
4
Tau-mediated neurodegeneration in Alzheimer's disease and related disorders.阿尔茨海默病及相关疾病中tau蛋白介导的神经退行性变。
Nat Rev Neurosci. 2007 Sep;8(9):663-72. doi: 10.1038/nrn2194.
5
Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's disease.种族在帕金森病中对微管相关蛋白tau(MAPT)H1单倍型和亚单倍型关联的作用。
Eur J Hum Genet. 2007 Nov;15(11):1163-8. doi: 10.1038/sj.ejhg.5201901. Epub 2007 Jul 18.
6
The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts.微管相关蛋白tau(MAPT)H1c风险单倍型与tau蛋白表达增加有关,尤其是与含4个重复序列的转录本表达增加有关。
Neurobiol Dis. 2007 Mar;25(3):561-70. doi: 10.1016/j.nbd.2006.10.018. Epub 2006 Dec 15.
7
Standardized subsets of the HGDP-CEPH Human Genome Diversity Cell Line Panel, accounting for atypical and duplicated samples and pairs of close relatives.HGDP-CEPH人类基因组多样性细胞系面板的标准化子集,包括非典型和重复样本以及近亲对。
Ann Hum Genet. 2006 Nov;70(Pt 6):841-7. doi: 10.1111/j.1469-1809.2006.00285.x.
8
Visualization of MAPT inversion on stretched chromosomes of tau-negative frontotemporal dementia patients.tau蛋白阴性额颞叶痴呆患者伸展染色体上MAPT倒位的可视化。
Hum Mutat. 2006 Oct;27(10):1057-9. doi: 10.1002/humu.20391.
9
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.一种与常见倒位多态性相关的新型17号染色体q21.31微缺失综合征。
Nat Genet. 2006 Sep;38(9):999-1001. doi: 10.1038/ng1853. Epub 2006 Aug 13.
10
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability.17号染色体长臂21.3区包含微管相关蛋白tau(MAPT)基因的微缺失与发育迟缓及学习障碍相关。
Nat Genet. 2006 Sep;38(9):1032-7. doi: 10.1038/ng1858. Epub 2006 Aug 13.

人类 17q21 倒位的分布和最近共同祖先。

The distribution and most recent common ancestor of the 17q21 inversion in humans.

机构信息

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

出版信息

Am J Hum Genet. 2010 Feb 12;86(2):161-71. doi: 10.1016/j.ajhg.2010.01.007. Epub 2010 Jan 28.

DOI:10.1016/j.ajhg.2010.01.007
PMID:20116045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2820164/
Abstract

The polymorphic inversion on 17q21, sometimes called the microtubular associated protein tau (MAPT) inversion, is an approximately 900 kb inversion found primarily in Europeans and Southwest Asians. We have identified 21 SNPs that act as markers of the inverted, i.e., H2, haplotype. The inversion is found at the highest frequencies in Southwest Asia and Southern Europe (frequencies of approximately 30%); elsewhere in Europe, frequencies vary from < 5%, in Finns, to 28%, in Orcadians. The H2 inversion haplotype also occurs at low frequencies in Africa, Central Asia, East Asia, and the Americas, though the East Asian and Amerindian alleles may be due to recent gene flow from Europe. Molecular evolution analyses indicate that the H2 haplotype originally arose in Africa or Southwest Asia. Though the H2 inversion has many fixed differences across the approximately 900 kb, short tandem repeat polymorphism data indicate a very recent date for the most recent common ancestor, with dates ranging from 13,600 to 108,400 years, depending on assumptions and estimation methods. This estimate range is much more recent than the 3 million year age estimated by Stefansson et al. in 2005.

摘要

17q21 上的多态性倒位,有时称为微管相关蛋白 tau(MAPT)倒位,是一种约 900 kb 的倒位,主要存在于欧洲人和西南亚人中。我们已经确定了 21 个 SNP,它们是倒置的标记,即 H2 单倍型。该倒位在西南亚和南欧的频率最高(约 30%);在欧洲其他地区,频率从芬兰的<5%到奥克尼群岛的 28%不等。H2 倒位单倍型在非洲、中亚、东亚和美洲的频率也较低,尽管东亚和美洲印第安人的等位基因可能是由于最近从欧洲传入的基因流所致。分子进化分析表明,H2 单倍型最初起源于非洲或西南亚。尽管 H2 倒位在大约 900 kb 的范围内有许多固定差异,但短串联重复多态性数据表明,最近的共同祖先出现的时间非常近,具体日期范围为 13600 至 108400 年,具体取决于假设和估计方法。这一估计范围比 Stefansson 等人在 2005 年估计的 300 万年要新得多。