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巴基斯坦葡萄糖-6-磷酸脱氢酶基因1311 C/T多态性的群体研究——对715条X染色体的分析

Population study of 1311 C/T polymorphism of Glucose 6 Phosphate Dehydrogenase gene in Pakistan - an analysis of 715 X-chromosomes.

作者信息

Moiz Bushra, Nasir Amna, Moatter Tariq, Naqvi Zulfiqar Ali, Khurshid Mohammad

机构信息

Department of Pathology and Microbiology, Aga Khan University, Karachi, Pakistan.

出版信息

BMC Genet. 2009 Jul 30;10:41. doi: 10.1186/1471-2156-10-41.

Abstract

BACKGROUND

Nucleotide 1311 polymorphism at exon 11 of G6PD gene is widely prevalent in various populations of the world. The aim of the study was to evaluate 1311 polymorphism in subjects carrying G6PD Mediterranean gene and in general population living in Pakistan.

RESULTS

Patients already known to be G6PD deficient were tested for 563C-T (G6PD Mediterranean) and 1311 C-T mutation through RFLP based PCR and gene sequencing. A control group not known to be G6PD deficient was tested for 1311C/T only.C-T transition at nt 1311 was detected in 60/234 X-chromosomes with 563 C-T mutation (gene frequency of 0.26) while in 130 of normal 402 X-chromosomes (gene frequency of 0.32).

CONCLUSION

We conclude that 1311 T is a frequent polymorphism both in general populations and in subjects with G6PD Mediterranean gene in Pakistan. The prevalence is higher compared to most of the populations of the world. The present study will help in understanding genetic basis of G6PD deficiency in Pakistani population and in developing ancestral links of its various ethnic groups.

摘要

背景

葡萄糖-6-磷酸脱氢酶(G6PD)基因第11外显子的1311位核苷酸多态性在世界各人群中广泛存在。本研究旨在评估携带G6PD地中海型基因的个体以及生活在巴基斯坦的普通人群中的1311多态性。

结果

通过基于限制性片段长度多态性(RFLP)的聚合酶链反应(PCR)和基因测序,对已知G6PD缺乏的患者进行563C-T(G6PD地中海型)和1311 C-T突变检测。对未知G6PD缺乏的对照组仅进行1311C/T检测。在234条携带563 C-T突变的X染色体中,有60条检测到1311位核苷酸的C-T转换(基因频率为0.26);而在402条正常X染色体中的130条中检测到该转换(基因频率为0.32)。

结论

我们得出结论,在巴基斯坦普通人群和携带G6PD地中海型基因的个体中,1311 T是一种常见的多态性。与世界上大多数人群相比,其患病率更高。本研究将有助于了解巴基斯坦人群中G6PD缺乏的遗传基础,并有助于建立其不同种族的祖先联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/2725355/1e4100363596/1471-2156-10-41-1.jpg

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