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印度奥里萨邦三个部落群体中三个VNTR基因座的遗传变异。

Genetic variation at three VNTR loci in three tribal populations of Orissa, India.

作者信息

Das K, Mastana S S

机构信息

Anthropology and Human Genetics Unit, Indian Statistical Institute, Kolkata, India.

出版信息

Ann Hum Biol. 2003 May-Jun;30(3):237-49. doi: 10.1080/0301446031000064512.

Abstract

BACKGROUND

The variable number of tandem repeats (VNTR) loci are robust, simple and rapid tools for genetic characterization of both individuals and populations. This paper presents data on the distribution of three VNTRs (APOB, YNZ22 and D1S80) in three tribal populations (Gadaba, Kuvi-Khond and Paroja) of the Koraput district of Orissa, India with a view to enlarge our understanding of molecular genetic diversity among these tribes and the usage of these VNTRs in anthropogenetic studies.

SUBJECTS AND METHODS

Three tribal populations were genotyped for APOB, YNZ22 and D1S80 loci using the polymerase chain reaction (PCR) technique. Gadaba are an Austro-Asiatic tribe while Kuvi-Khond and Paroja are Dravidian tribes. All samples were collected, with consent, from unrelated individuals.

RESULTS

The observed allelic variation in these tribes is comparable with many Indian populations, but they showed significant overall and inter-population variability within the region. Allele *24 was the most common allele at the D1S80 locus in all populations, with Gadabas having the highest frequency (50%) followed by Paroja (32%) and Kuvi-Khond (23%). Gadabas also showed a higher frequency of allele *19 (13%) and *31 (9%) compared to other Indian and European populations. In the Apo B system, allele *37 was the most common in all three populations, with Gadabas having the highest frequency (39%) followed by Paroja (24%) and Kuvi-Khond (21%). This allele is present in high frequencies in other Indian (except Gonds) and European populations. Alleles *33 (17%), *35 (20%) and *45 (12%) were also common in the Gadabas, but Kuvi-Khond showed higher frequencies of *31(10%), *35(13%) and the larger allele *49(16%). Paroja, on the other hand, had higher frequencies of *31 (14%), *33 (17%) and *45 (13%). Allele *49 was also present in Paroja (10%) but was absent in the Gadaba. For the YNZ22 system, allele *4 was the most common in Kuvi-Khond (25%) and Paroja (21.4%), and allele *2 was the predominant allele in the Gadaba (33%). However allele *4 still occurs at relatively high frequency in Gadaba (27%). Allele *2 also occurs at relatively high frequency in Kuvi-Khond (20%) and intermediate frequency in Paroja (11%). Average heterozygosity was relatively low for Gadaba (0.7597 +/- 0.0191) and high for Kuvi-Khond (0.8618 +/- 0.0149) and Paroja (0.8512 +/- 0.0190), perhaps a reflection of effective population size and limitations to mating. The level of gene differentiation is, however, low (3-4%) for the three systems studied in these tribal populations and in data compiled from previous studies from the region.

CONCLUSIONS

The VNTRs are polymorphic in the tribal populations studied and there is extensive allelic variation. Gadabas are isolated but Kuvi-Khond and Paroja show clear affinities with the Gonds, a major tribal group of Central India. Overall, allele frequency distribution, heterozygosity and genetic diversity analysis show that genetic diversity observed is socially, linguistically and geographically structured in this region.

摘要

背景

可变串联重复序列(VNTR)位点是用于个体和群体遗传特征分析的强大、简单且快速的工具。本文呈现了印度奥里萨邦科拉普特地区三个部落群体(加达巴、库维 - 孔德和帕罗贾)中三个VNTR(载脂蛋白B基因、YNZ22和D1S80)的分布数据,旨在加深我们对这些部落间分子遗传多样性以及这些VNTR在人类遗传学研究中应用的理解。

对象与方法

使用聚合酶链反应(PCR)技术对三个部落群体的载脂蛋白B基因、YNZ22和D1S80位点进行基因分型。加达巴是一个南亚语系部落,而库维 - 孔德和帕罗贾是达罗毗荼部落。所有样本均在获得同意后从无亲缘关系的个体中采集。

结果

这些部落中观察到的等位基因变异与许多印度人群相当,但在该地区内总体和群体间显示出显著的变异性。等位基因24是所有群体中D1S80位点最常见的等位基因,加达巴人频率最高(50%),其次是帕罗贾人(32%)和库维 - 孔德人(23%)。与其他印度和欧洲人群相比,加达巴人等位基因19(13%)和31(9%)的频率也更高。在载脂蛋白B系统中,等位基因37在所有三个群体中最常见,加达巴人频率最高(39%),其次是帕罗贾人(24%)和库维 - 孔德人(21%)。该等位基因在其他印度人群(除贡德人外)和欧洲人群中频率较高。等位基因33(17%)、35(20%)和45(12%)在加达巴人中也很常见,但库维 - 孔德人31(10%)、35(13%)和较大的等位基因49(16%)频率更高。另一方面,帕罗贾人31(14%)、33(17%)和45(13%)频率较高。等位基因49在帕罗贾人中也有出现(10%),但在加达巴人中不存在。对于YNZ22系统,等位基因4在库维 - 孔德人(25%)和帕罗贾人(21.4%)中最常见,等位基因2在加达巴人中占主导(33%)。然而,等位基因4在加达巴人中仍以相对较高频率出现(27%)。等位基因2在库维 - 孔德人中也以相对较高频率出现(20%),在帕罗贾人中出现频率中等(11%)。加达巴人的平均杂合度相对较低(0.7597±0.0191),库维 - 孔德人(0.8618±0.0149)和帕罗贾人(0.8512±0.0190)较高,这可能反映了有效种群大小和交配限制。然而,在这些部落群体以及该地区先前研究汇编的数据中,所研究的三个系统的基因分化水平较低(3 - 4%)。

结论

在所研究的部落群体中,VNTR具有多态性且存在广泛的等位基因变异。加达巴人较为孤立,但库维 - 孔德人和帕罗贾人与印度中部的主要部落群体贡德人有明显的亲缘关系。总体而言,等位基因频率分布、杂合度和遗传多样性分析表明,该地区观察到的遗传多样性在社会、语言和地理上具有结构特征。

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