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太平洋地区人类线粒体DNA中COII/tRNALys基因间9个碱基对缺失的进化史。

Evolutionary history of the COII/tRNALys intergenic 9 base pair deletion in human mitochondrial DNAs from the Pacific.

作者信息

Redd A J, Takezaki N, Sherry S T, McGarvey S T, Sofro A S, Stoneking M

机构信息

Department of Anthropology, Pennsylvania State University, University Park 16802, USA.

出版信息

Mol Biol Evol. 1995 Jul;12(4):604-15. doi: 10.1093/oxfordjournals.molbev.a040240.

Abstract

Length changes in human mitochondrial DNA (mtDNA) are potentially useful markers for inferring the evolutionary history of populations. One such length change is a nine base pair (9-bp) deletion that is located in the intergenic region between the COII gene and the Lysine tRNA gene (COII/tRNALys intergenic region). This deletion has been used as a genetic marker to trace descent from peoples of East Asian origin. A geographic cline of the deletion frequency across modern Pacific Islander populations suggests that the deletion may be useful for tracing prehistoric Polynesian origins and affinities. Mitochondrial DNA sequence variation within two variable segments of the control region (CR) permits a number of inferences regarding the evolutionary history of the 9-bp deletion that cannot be determined from frequency data alone. We obtained CR sequences from 74 mtDNAs with the 9-bp deletion from Indonesia, coastal Papua New Guinea (PNG), and American Samoa. Phylogenetic and pairwise distribution analysis of these CR sequences pooled with previously published CR sequences reveals that the deletion arose independently in Africa and Asia and suggests possible multiple origins of the deletion in Asia. A clinal increase of the frequency of the 9-bp deletion across the three Pacific populations is associated with a decrease in CR sequence diversity, consistent with founder events. Furthermore, analysis of pairwise difference distributions indicates an expansion time of proto-Polynesians that began 5,500 yr ago from Southeast Asia. These results are consistent with the express train model of Polynesian origins.

摘要

人类线粒体DNA(mtDNA)的长度变化是推断种群进化历史的潜在有用标记。一种这样的长度变化是位于细胞色素氧化酶亚基II基因(COII)和赖氨酸转运RNA基因(COII/tRNALys基因间隔区)之间基因间隔区的9个碱基对(9-bp)缺失。这种缺失已被用作遗传标记来追溯东亚起源人群的血统。现代太平洋岛民群体中缺失频率的地理渐变表明,这种缺失可能有助于追溯史前波利尼西亚人的起源和亲缘关系。控制区(CR)两个可变区段内的线粒体DNA序列变异允许对9-bp缺失的进化历史进行一些仅从频率数据无法确定的推断。我们从印度尼西亚、巴布亚新几内亚沿海(PNG)和美属萨摩亚的74个带有9-bp缺失的线粒体DNA中获得了CR序列。对这些CR序列与先前发表的CR序列进行系统发育和成对分布分析表明,该缺失在非洲和亚洲独立出现,并表明该缺失在亚洲可能有多个起源。三个太平洋群体中9-bp缺失频率的渐变增加与CR序列多样性的降低相关,这与奠基者事件一致。此外,成对差异分布分析表明,原波利尼西亚人的扩张始于5500年前的东南亚。这些结果与波利尼西亚起源的特快列车模型一致。

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