Shields G F, Hecker K, Voevoda M I, Reed J K
Institute of Arctic Biology, University of Alaska, Fairbanks.
Am J Hum Genet. 1992 Apr;50(4):758-65.
The Asian-specific 9-bp deletion between the genes for mitochondrial cytochrome oxidase II and lysine transfer RNA has been used to trace aboriginal human movements out of Southeast Asia and into portions of the South Pacific. Although it has been used to estimate the number of independent lineages that occur in the New World, it has not been studied in native peoples of the Beringian region. Thus, we have used PCR to amplify and compare the lengths of DNA segments surrounding this deletion in native peoples of Beringia and the adjacent regions, as well as natives of the Altai Mountains of Southwestern Siberia. Of the 176 individuals analyzed here, the deletion was found in only 3 of 25 individuals from the Ust-Kan region of the Altai Mountains. We comment on the distribution of this marker and on potential relationships between Beringians and other Native American groups in which this marker has been surveyed. One Chukchi possessed three copies of the 9-bp sequence, which suggests (1) that the number of copies of this sequence in humans may be more variable than had been believed and (2) that a mechanism of replication based on tandem duplication may be a potential explanation for the origin of this length mutation in humans.
线粒体细胞色素氧化酶II基因和赖氨酸转移RNA基因之间亚洲特有的9个碱基对缺失,已被用于追踪人类从东南亚迁出并进入南太平洋部分地区的原始迁徙情况。尽管它已被用于估计新世界中独立谱系的数量,但尚未在白令地区的原住民中进行研究。因此,我们利用聚合酶链反应(PCR)扩增并比较了白令地区及邻近地区原住民以及西伯利亚西南部阿尔泰山脉原住民中该缺失周围DNA片段的长度。在本文分析的176个人中,仅在阿尔泰山脉乌斯季坎地区的25个人中的3个人中发现了该缺失。我们对该标记的分布以及白令人与其他已对该标记进行过调查的美洲原住民群体之间的潜在关系进行了评论。一名楚科奇人拥有该9个碱基对序列的三个拷贝,这表明(1)该序列在人类中的拷贝数可能比之前认为的更具可变性,以及(2)基于串联重复的复制机制可能是该长度突变在人类中起源的一个潜在解释。