Contribution of M470V variant to cystic fibrosis: First study in CF and normal Tunisian population

M. Nefzi , S. Hadj Fredj , N. Tebib , S. Barsaoui , K. Boussetta , H. Siala , T. Messaoud
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引用次数: 4

Abstract

Purpose

Determining the frequency of M470V polymorphism in cystic fibrosis and healthy cohort in Tunisia to establish the contribution of M470V polymorphism in cystic fibrosis variable presentation and course. Additionally, studying the origin of cystic fibrosis transmembrane conductance regulator gene in Tunisian population and its evolution among populations worldwide.

Patients and methods

The genotyping of M470V marker was realized by PCR-RFLP technique in 34 unrelated patients and 50 healthy subjects.

Results

Statistical difference was found in the genotype and allelic distribution between CF and control groups. Exclusive association between F508del allele and M470 allele was noted.

Conclusion

This study has contributed to better understanding involvement of the M470V polymorphism in the CF clinical expression in the Tunisian population and has confirmed the utility of this marker in the study of the origin and evolution of the CFTR locus in the human history.

M470V变异对囊性纤维化的贡献:首次在CF和正常突尼斯人群中进行的研究
目的测定突尼斯人群囊性纤维化和健康人群中M470V多态性的频率,确定M470V多态性在囊性纤维化变量表现和病程中的贡献。此外,研究突尼斯人群囊性纤维化跨膜传导调节基因的起源及其在世界人群中的进化。患者与方法采用PCR-RFLP技术对34例无亲缘关系患者和50例健康对照者的M470V标记物进行基因分型。结果CF组与对照组基因型及等位基因分布差异有统计学意义。F508del等位基因与M470等位基因之间存在排他性关联。结论本研究有助于更好地理解M470V多态性在突尼斯人群CF临床表达中的作用,并证实了该标记在研究CFTR基因座在人类历史上的起源和进化中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pathologie-biologie
Pathologie-biologie 医学-病理学
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6-12 weeks
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