Mitochondrial DNA sequence polymorphisms of five ethnic populations from northern China

被引:139
作者
Kong, QP
Yao, YG
Liu, M
Shen, SP
Chen, C
Zhu, CL
Palanichamy, MG
Zhang, YP [1 ]
机构
[1] Chinese Acad Sci, Kunming Inst Zool, Lab Cellular & Mol Evolut, Kunming 650223, Peoples R China
[2] Yunnan Univ, Lab Conservat & Utilizat Bioresource, Kunming 650091, Peoples R China
[3] Baotou Med Coll, Dept Pathol, Baotou 014010, Mongolia
基金
中国国家自然科学基金;
关键词
D O I
10.1007/s00439-003-1004-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To study the mitochondrial DNA (mtDNA) polymorphisms in a total of 232 individuals from five ethnic populations (Daur, n=45; Ewenki, n=47; Korean, n=48; Mongolian, n=48; Oroqen, n=44) in northern China, we analyzed the control region sequences and typed for a number of characteristic mutations in coding regions (especially the region 14576-16047), by direct sequencing or restriction-fragment-length-polymorphism (RFLP) analysis. With the exception of 14 individuals belonging to the European-specific haplogroups R2, H, J, and T, the mtDNAs considered could be assigned into the East Asian-specific haplogroups described recently. The polymorphisms in cytochrome b sequence were found to be very informative for defining or supporting the haplogroups status of East Asian mtDNAs in addition to the reported regions 10171-10659 and 14055-14590 in our previous study. The haplogroup distribution frequencies varied in the five ethnic populations, but in general they all harbored a large amount of north-prevalent haplogroups, such as D, G, C, and Z, and thus were in agreement with their ethnohistory of northern origin. The two populations (Ewenki and Oroqen) with small population census also show concordant features in their matrilineal genetic structures, with lower genetic diversities observed.
引用
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页码:391 / 405
页数:15
相关论文
共 34 条
[1]   Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA [J].
Andrews, RM ;
Kubacka, I ;
Chinnery, PF ;
Lightowlers, RN ;
Turnbull, DM ;
Howell, N .
NATURE GENETICS, 1999, 23 (02) :147-147
[2]   Detecting errors in mtDNA data by phylogenetic analysis [J].
Bandelt, HJ ;
Lahermo, P ;
Richards, M ;
Macaulay, V .
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 2001, 115 (02) :64-69
[3]   The fingerprint of phantom mutations in mitochondrial DNA data [J].
Bandelt, HJ ;
Quintana-Murci, L ;
Salas, A ;
Macaulay, V .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (05) :1150-1160
[4]  
BANDELT HJ, 2003, IN PRESS ANN HUM GEN
[5]   Proposed guidelines for papers describing DNA polymorphism-disease associations [J].
Cooper, DN ;
Nussbaum, RL ;
Krawczak, M .
HUMAN GENETICS, 2002, 110 (03) :207-208
[6]   Nomenclature for the description of human sequence variations [J].
den Dunnen, JT ;
Antonarakis, E .
HUMAN GENETICS, 2001, 109 (01) :121-124
[7]   Population structure and history in East Asia [J].
Ding, YC ;
Wooding, S ;
Harpending, HC ;
Chi, HC ;
Li, HP ;
Fu, YX ;
Pang, JF ;
Yao, YG ;
Yu, JGX ;
Moyzis, R ;
Zhang, YP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (25) :14003-14006
[8]  
Du, 1993, ETHNIC GROUPS CHINA
[9]   Phylogenetic network for European mtDNA [J].
Finnilä, S ;
Lehtonen, MS ;
Majamaa, K .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (06) :1475-1484
[10]  
Herrnstadt, 2002, AM J HUM GENET, V71, P448