Interrogating multiple aspects of variation in a full resequencing data set to infer human population size changes

被引:219
作者
Voight, BF
Adams, AM
Frisse, LA
Qian, YD
Hudson, RR
Di Rienzo, A
机构
[1] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Ecol & Evolut, Chicago, IL 60637 USA
[3] Univ Chicago, Comm Genet, Chicago, IL 60637 USA
关键词
bottlenecks; combining P values; human demographic inference; population growth;
D O I
10.1073/pnas.0507325102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We present an expanded data set of 50 unlinked autosomal noncoding regions, resequenced in samples of Hausa from Cameroon, Italians, and Chinese. We use these data to make inferences about human demographic history by using a technique that combines multiple aspects of genetic data, including levels of polymorphism, the allele frequency spectrum, and linkage disequilibrium. We explore an extensive range of demographic parameters and demonstrate that our method of combining multiple aspects of the data results in a significant reduction of the compatible parameter space. In agreement with previous reports, we find that the Hausa data are compatible with demographic equilibrium as well as a set of recent population expansion models. In contrast to the Hausa, when multiple aspects of the data are considered jointly, the non-Africans depart from an equilibrium model of constant population size and are compatible with a range of simple bottleneck models, including a 50-90% reduction in effective population size occurring some time after the appearance of modern humans in Africa 160,000-120,000 years ago.
引用
收藏
页码:18508 / 18513
页数:6
相关论文
共 52 条
[21]  
Kuhner MK, 1998, GENETICS, V149, P429
[22]  
Lahr MM, 1998, YEARB PHYS ANTHROPOL, V41, P137
[23]   Sequence variations in the public human genome data reflect a bottlenecked population history [J].
Marth, G ;
Schuler, G ;
Yeh, R ;
Davenport, R ;
Agarwala, R ;
Church, D ;
Wheelan, S ;
Baker, J ;
Ward, M ;
Kholodov, M ;
Phan, L ;
Czabarka, E ;
Murvai, J ;
Cutler, D ;
Wooding, S ;
Rogers, A ;
Chakravarti, A ;
Harpending, HC ;
Kwok, PY ;
Sherry, ST .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (01) :376-381
[24]   The allele frequency spectrum in genome-wide human variation data reveals signals of differential demographic history in three large world populations [J].
Marth, GT ;
Czabarka, E ;
Murvai, J ;
Sherry, ST .
GENETICS, 2004, 166 (01) :351-372
[25]   The fine-scale structure of recombination rate variation in the human genome [J].
McVean, GAT ;
Myers, SR ;
Hunt, S ;
Deloukas, P ;
Bentley, DR ;
Donnelly, P .
SCIENCE, 2004, 304 (5670) :581-584
[26]   PolyPhred: Automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing [J].
Nickerson, DA ;
Tobe, VO ;
Taylor, SL .
NUCLEIC ACIDS RESEARCH, 1997, 25 (14) :2745-2751
[27]  
Nielsen R, 2000, GENETICS, V154, P931
[28]  
Nielsen Rasmus, 2004, Human Genomics, V1, P218
[29]  
Pluzhnikov A, 2002, GENETICS, V161, P1209
[30]   Adjusting the focus on human variation [J].
Przeworski, M ;
Hudson, RR ;
Di rienzo, A .
TRENDS IN GENETICS, 2000, 16 (07) :296-302