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

被引:21
作者
Moiz, Bushra [1 ]
Nasir, Amna [1 ]
Moatter, Tariq [1 ]
Naqvi, Zulfiqar Ali [2 ]
Khurshid, Mohammad [1 ]
机构
[1] Aga Khan Univ, Dept Pathol & Microbiol, Karachi, Pakistan
[2] Aga Khan Univ, Res Off, Karachi, Pakistan
来源
BMC GENETICS | 2009年 / 10卷
关键词
CONSANGUINEOUS MARRIAGES; DEHYDROGENASE DEFICIENCY; G6PD; ORIGIN; LOCALIZATION; PREVALENCE; MUTATIONS; VARIANTS; MARKER; PATHAN;
D O I
10.1186/1471-2156-10-41
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
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页数:7
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