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

نویسندگان

  • Michael P Donnelly
  • Peristera Paschou
  • Elena Grigorenko
  • David Gurwitz
  • Syed Qasim Mehdi
  • Sylvester L B Kajuna
  • Csaba Barta
  • Selemani Kungulilo
  • N J Karoma
  • Ru-Band Lu
  • Olga V Zhukova
  • Jong-Jin Kim
  • David Comas
  • Marcello Siniscalco
  • Maria New
  • Peining Li
  • Hui Li
  • Vangelis G Manolopoulos
  • William C Speed
  • Haseena Rajeevan
  • Andrew J Pakstis
  • Judith R Kidd
  • Kenneth K Kidd
چکیده

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.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Using the neanderthal and denisova genetic data to understand the common MAPT 17q21 inversion in modern humans.

The polymorphic inversion on 17q21, that includes the MAPT gene, represents a unique locus in the human genome characterized by a large region with strong linkage disequilibrium. Two distinct haplotypes, H1 and H2, exist in modern humans, and H1 has been unequivocally related to several neurodegenerative disorders. Recent data indicate that recurrent inversions of this genomic region have occur...

متن کامل

Pulse-Field Gel Electrophoresis (PFGE) of Salmonella Serovar Infantis Isolates From Poultry

Background: Salmonella is one of the most important zoonotic agents known to infect humans and a wide range of animals, including poultry. Salmonella Infantis has been one of the 15 most frequently isolated serovars throughout the world. Despite its clinical importance, little is known about the molecular characteristics of S. Infantis strains from Iran. OBJECTIVES: The purpose of this study wa...

متن کامل

Reassessing the Evolutionary History of the 17q21 Inversion Polymorphism

A polymorphic inversion that lies on chromosome 17q21 comprises two major haplotype families (H1 and H2) that not only differ in orientation but also in copy-number. Although the processes driving the spread of the inversion-associated lineage (H2) in humans remain unclear, a selective advantage has been proposed for one of its subtypes. Here, we genotyped a large panel of individuals from prev...

متن کامل

A Direct Matrix Inversion-Less Analysis for Distribution System Power Flow Considering Distributed Generation

This paper presents a new direct matrix inversion-less analysis for radial distribution systems (RDSs). The method can successfully deal with weakly meshed distribution systems. (WMDSs). Being easy to implement, direct methods (DMs) provide an excellent performance. Matrix inversion is the mean reason of divergence and low-efficiency in power flow algorithms. In this paper, the performance of t...

متن کامل

The Time Back to the Most Recent Common Ancestor in Exchangeable Population Models

A class of haploid population models with non-overlapping generations and exchangeable offspring distribution is considered. Based on an analysis of the discrete ancestral process, we present solutions, algorithms and strong upper bounds for the expected time back to the most recent common ancestor. New insights into the asymptotical behavior of the expected time back to the most recent common ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • American journal of human genetics

دوره 86 2  شماره 

صفحات  -

تاریخ انتشار 2010