Testing multiregionality of modern human origins

被引:62
作者
Takahata, N [1 ]
Lee, SH [1 ]
Satta, Y [1 ]
机构
[1] Grad Univ Adv Studies, Dept Biosyst Sci, Hayama, Kanagawa 2400193, Japan
关键词
D O I
10.1093/oxfordjournals.molbev.a003791
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In order to examine the possibility of multiple founding populations of anatomically modern Home sapiens, we collected DNA sequence data from 10 X-chromosomal regions, 5 autosomal regions, and 1 Y-chromosomal region, in addition to mitochondrial DNA. Except for five regions which are genealogically uninformative and two other regions for which chimpanzee orthologs are not available, the ancestral sequence and population for each of the remaining regions were successfully inferred. Of these 10 ancestral sequences, 9 occurred in Africa and only I occurred in Asia during the Pleistocene. Computer simulation was carried out to quantify the multiregional hypothesis based solely on the premise that there was more than one founding population in the Pleistocene. Allowing the breeding size to vary among the founding populations, the hypothesis may account for the observed African ancestry in 90% of the genomic regions. However, it is required that the founding population in Africa was much larger than that outside Africa. Likelihood estimates of the breeding sizes in the founding populations were more than 9,000 in Africa and less than 1,000 in outside of Africa, although these estimates can be much less biased at the 1% significance level. If the number of African ancestral sequences further increases as more data accumulate in other genomic regions, the conclusion of a single founding population of modern H. sapiens is inevitable.
引用
收藏
页码:172 / 183
页数:12
相关论文
共 58 条
[1]   DNA variation in a 5-Mb region of the X chromosome and estimates of sex-specific/type-specific mutation rates [J].
Anagnostopoulos, T ;
Green, PM ;
Rowley, G ;
Lewis, CM ;
Giannelli, F .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (02) :508-517
[2]   MITOCHONDRIAL-DNA AND HUMAN-EVOLUTION [J].
CANN, RL ;
STONEKING, M ;
WILSON, AC .
NATURE, 1987, 325 (6099) :31-36
[3]  
Cavalli-Sforza L. L., 1994, HIST GEOGRAPHY HUMAN
[4]   Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase [J].
Clark, AG ;
Weiss, KM ;
Nickerson, DA ;
Taylor, SL ;
Buchanan, A ;
Stengård, J ;
Salomaa, V ;
Vartiainen, E ;
Perola, M ;
Boerwinkle, E ;
Sing, CF .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (02) :595-612
[5]  
Coon CarletonS., 1962, ORIGIN RACES
[6]   ANCESTRAL INFERENCE IN POPULATION-GENETICS [J].
GRIFFITHS, RC ;
TAVARE, S .
STATISTICAL SCIENCE, 1994, 9 (03) :307-319
[7]   SAMPLING THEORY FOR NEUTRAL ALLELES IN A VARYING ENVIRONMENT [J].
GRIFFITHS, RC ;
TAVARE, S .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1994, 344 (1310) :403-410
[8]   A mathematical theory of natural and artificial selection, Part V: Selection and mutation. [J].
Haldane, JBS .
PROCEEDINGS OF THE CAMBRIDGE PHILOSOPHICAL SOCIETY, 1927, 23 :838-844
[9]   Out of Africa and back again: Nested cladistic analysis of human Y chromosome variation [J].
Hammer, MF ;
Karafet, T ;
Rasanayagam, A ;
Wood, ET ;
Altheide, TK ;
Jenkins, T ;
Griffiths, RC ;
Templeton, AR ;
Zegura, SL .
MOLECULAR BIOLOGY AND EVOLUTION, 1998, 15 (04) :427-441
[10]  
Hammer MF, 1997, GENETICS, V145, P787