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委内瑞拉瓜希沃美洲印第安人群体中的线粒体序列变异。

Mitochondrial sequence variation in the Guahibo Amerindian population from Venezuela.

作者信息

Vona Giuseppe, Falchi Alessandra, Moral Pedro, Calò Carla M, Varesi Laurent

机构信息

Department of Experimental Biology, Section of Anthropological Sciences, University of Cagliari, 09042 Cagliari, Italy.

出版信息

Am J Phys Anthropol. 2005 Jul;127(3):361-9. doi: 10.1002/ajpa.20070.

Abstract

New data were obtained on mitochondrial DNA (mtDNA) from Guahibo from Venezuela, a group so far not studied using molecular data. A population sample (n = 59) was analyzed for mtDNA variation in two control-region hypervariable segments (HV1 and HV2) by sequencing. The presence or absence of a 9-bp polymorphism in the COII/tRNA(Lys) region was studied by direct amplification and electrophoretic identification. Thirty-eight variable sites were detected in regions HV1 and HV2, defining 26 mtDNA lineages; 23.7% of these were present in a single individual. The 9-bp deletion was found in 3.39% of individuals. Nucleotide and haplotype diversities were relatively high compared with other New World populations. The identified sequence haplotypes were classified into four major haplogroups (A-D) according to previous studies, with high frequencies for A (47.46%) and C (49.15%), low frequency for B (3.39%), and an absence of D.

摘要

获得了来自委内瑞拉瓜希沃人的线粒体DNA(mtDNA)新数据,该群体迄今为止尚未使用分子数据进行研究。通过测序分析了一个群体样本(n = 59)在两个控制区高变段(HV1和HV2)中的mtDNA变异。通过直接扩增和电泳鉴定研究了COII/tRNA(Lys)区域中9个碱基多态性的存在与否。在HV1和HV2区域检测到38个可变位点,定义了26个mtDNA谱系;其中23.7%仅存在于单个个体中。在3.39%的个体中发现了9个碱基的缺失。与其他新大陆人群相比,核苷酸和单倍型多样性相对较高。根据先前的研究,所鉴定的序列单倍型被分为四个主要单倍群(A - D),其中A(47.46%)和C(49.15%)频率较高,B(3.39%)频率较低,且未发现D单倍群。

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