Suppr超能文献

成都地区汉族人群中MC1R基因多态性与雀斑的关联研究

[Association study of MC1R gene polymorphisms with freckles in Chinese Han population from Chengdu].

作者信息

Cao Liping, Ye Yi, Cong Ruijuan, Wu Jin, Li Yingbi, Liao Miao, Yan Jing

机构信息

Department of Forensic Genetics, West China School of Basic Science and Forensic Medicine, Sichuan University, Chengdu, Sichuan 610041, P.R. China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Jun;30(3):352-6. doi: 10.3760/cma.j.issn.1003-9406.2013.03.022.

Abstract

OBJECTIVE

To assess the association between single nucleotide polymorphisms (SNPs) of melanocortin-1 receptor gene (MC1R) and freckles in Chinese Han population from Chengdu.

METHODS

Twenty randomly selected samples were used to select SNPs of the MC1R gene through DNA sequencing. Pyrosequencing in combination with DNA pooling technique was used to assess allelic frequencies of the selected SNPs in 111 individuals with freckles and 124 normal controls. Representative SNPs were selected based on their functional implications and minimum allele frequency (MAF> 0.05). Genotype of the SNPs were determined with polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) or pyrosequencing.

RESULTS

Based on results of DNA sequencing and pyrosequencing, 4 SNPs (rs2228479, rs885479, rs33932559 and rs2228478) were selected to determine the genotype for each sample. Comparison of genotypic and allelic frequencies of the 4 SNPs with χ (2) test has found no significant difference between the two groups (P> 0.05). For rs33932559, the frequencies of T allele were respectively 90.09% and 91.94% for individuals with freckles and normal controls. For rs2228479 and rs2228478, the frequencies of G and A allele were both about 77%. For rs885479, the frequency of T allele was about 60%. None of the above 3 SNPs showed a significant difference between the two groups in terms of allelic or genotypic frequencies.

CONCLUSION

No association between the selected SNPs of MC1R gene has been found with development of freckles for the selected Chinese Han population from Chengdu.

摘要

目的

评估成都汉族人群中黑素皮质素-1受体基因(MC1R)单核苷酸多态性(SNP)与雀斑之间的关联。

方法

通过DNA测序从20个随机选取的样本中筛选MC1R基因的SNP。采用焦磷酸测序结合DNA池技术评估111例雀斑患者和124例正常对照中所选SNP的等位基因频率。根据其功能意义和最小等位基因频率(MAF>0.05)选择代表性SNP。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)或焦磷酸测序法确定SNP的基因型。

结果

根据DNA测序和焦磷酸测序结果,选择4个SNP(rs2228479、rs885479、rs33932559和rs2228478)确定每个样本的基因型。采用χ(2)检验比较这4个SNP的基因型和等位基因频率,发现两组之间无显著差异(P>0.05)。对于rs33932559,雀斑患者和正常对照中T等位基因频率分别为90.09%和91.94%。对于rs2228479和rs2228478,G和A等位基因频率均约为77%。对于rs885479,T等位基因频率约为60%。上述3个SNP在等位基因或基因型频率方面两组之间均无显著差异。

结论

对于所选的成都汉族人群,未发现MC1R基因的所选SNP与雀斑的发生之间存在关联。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验