Department of Genetics, School of Medicine, Yale University, New Haven, CT 06520, USA.
Am J Hum Genet. 2010 Feb 12;86(2):161-71. doi: 10.1016/j.ajhg.2010.01.007. Epub 2010 Jan 28.
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.
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。