南印度健康人群DNA修复基因多态性的等位基因和基因型分布。

Biomarkers in cancer Pub Date : 2014-12-07 eCollection Date: 2014-01-01 DOI:10.4137/BIC.S19681
Katiboina Srinivasa Rao, Abialbon Paul, Annan Sudarsan Arun Kumar, Gurusamy Umamaheswaran, Biswajit Dubashi, Karunanithi Gunaseelan, Steven Aibor Dkhar
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引用次数: 9

摘要

各种DNA修复途径保护人类基因组的结构和化学完整性免受环境和内源性威胁。编码DNA修复蛋白的基因多态性已被发现与癌症风险和化疗反应有关。在本研究中,我们旨在建立南印度健康人群中DNA修复基因的规范频率,并与HapMap人群进行比较。对来自南印度的128名健康志愿者进行了基因分型,并建立了等位基因和基因型分布。着色性干皮病A组(XPA) G23A、切除修复交叉互补2组(ERCC2)/着色性干皮病D组(XPD) Lys751Gln、着色性干皮病G组(XPG) His46His、XPG Asp1104His和x射线修复交叉互补1组(XRCC1) Arg399Gln多态性的小等位基因频率分别为49.2%、36.3%、48.0%、23.0%和34.0%。这些多态性在南印度人和其他HapMap人群之间的频率分布中观察到种族差异。目前的工作为癌症关联研究和治疗反应和预后的生物标志物鉴定奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Allele and genotype distributions of DNA repair gene polymorphisms in South Indian healthy population.

Allele and genotype distributions of DNA repair gene polymorphisms in South Indian healthy population.

Allele and genotype distributions of DNA repair gene polymorphisms in South Indian healthy population.

Allele and genotype distributions of DNA repair gene polymorphisms in South Indian healthy population.

Various DNA repair pathways protect the structural and chemical integrity of the human genome from environmental and endogenous threats. Polymorphisms of genes encoding the proteins involved in DNA repair have been found to be associated with cancer risk and chemotherapeutic response. In this study, we aim to establish the normative frequencies of DNA repair genes in South Indian healthy population and compare with HapMap populations. Genotyping was done on 128 healthy volunteers from South India, and the allele and genotype distributions were established. The minor allele frequency of Xeroderma pigmentosum group A (XPA) G23A, Excision repair cross-complementing 2 (ERCC2)/Xeroderma pigmentosum group D (XPD) Lys751Gln, Xeroderma pigmentosum group G (XPG) His46His, XPG Asp1104His, and X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln polymorphisms were 49.2%, 36.3%, 48.0%, 23.0%, and 34.0% respectively. Ethnic variations were observed in the frequency distribution of these polymorphisms between the South Indians and other HapMap populations. The present work forms the groundwork for cancer association studies and biomarker identification for treatment response and prognosis.

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