Yao Y G, Watkins W S, Zhang Y P
Laboratory of Cellular and Molecular Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Yunnan.
Hum Genet. 2000 Nov;107(5):504-12. doi: 10.1007/s004390000403.
In total, 1218 Chinese from twelve ethnic groups and nine Han geographic groups were screened for the mtDNA 9-bp deletion motif. The frequency of the 9-bp deletion in all samples was 14.7% but ranged from 0% to 32% in the various ethnic groups. Three individuals had a triplication of the 9-bp segment. Phylogenetic and demographic analyses of the mtDNA hypervariable segment 1 (HVS 1) sequences suggest that the 9-bp deletion occurred more than once in China. The majority of the Chinese deletion haplotypes (about 90%) have a common origin as a mutational event following an initial expansion of modern humans in eastern Asia. Other deletion haplotypes and the three haplotypes with a 9-bp triplication may have arisen independently in the Chinese, presumably by replication error. HVS1 haplotype analysis suggests two possible migration routes of the 9-bp deletion in east and southeast Asia. Both migrations originated in China with one route leading to the Pacific Islands via Taiwan, the other to southeast Asia and possibly the Nicobar Islands. Along both routes of peopling, a decrease in HVSI diversity of the mtDNA haplotypes is observed. The "Polynesian motif (16217T/C, 16247A/G, and 16261C/T)" and the 16140T/C, 16266C/A, or C/G polymorphisms appear specific to each migration route.
总共对来自12个民族和9个汉族地理群体的1218名中国人进行了线粒体DNA 9碱基缺失基序筛查。所有样本中9碱基缺失的频率为14.7%,但在不同民族中从0%到32%不等。有3个人的9碱基片段出现了三倍重复。对线粒体DNA高变区1(HVS 1)序列的系统发育和人口统计学分析表明,9碱基缺失在中国不止一次发生。大多数中国缺失单倍型(约90%)有着共同起源,是现代人类在东亚最初扩张后发生的一次突变事件。其他缺失单倍型以及三种具有9碱基三倍重复的单倍型可能在中国独立出现,推测是由于复制错误。HVS1单倍型分析表明,9碱基缺失在东亚和东南亚有两条可能的迁移路线。两次迁移均起源于中国,一条路线经由台湾通向太平洋岛屿,另一条通向东南亚以及可能的尼科巴群岛。在两条人口迁移路线上,均观察到线粒体DNA单倍型HVSI多样性的降低。“波利尼西亚基序(16217T/C、16247A/G和16261C/T)”以及16140T/C、16266C/A或C/G多态性似乎对每条迁移路线具有特异性。