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中西方人群哮喘遗传学差异。

Differences in asthma genetics between Chinese and other populations.

机构信息

Department of Pediatrics, Chinese University of Hong Kong, Hong Kong, China.

Department of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong, China.

出版信息

J Allergy Clin Immunol. 2014 Jan;133(1):42-8. doi: 10.1016/j.jaci.2013.09.018. Epub 2013 Nov 1.

Abstract

Asthma is caused by complex gene-gene and gene-environment interactions. Most asthma genes are not replicable across populations, which is possibly because of differences in the epidemiology of these genes. Our case-control association and next-generation sequencing studies revealed substantial discrepancies in the frequencies of single nucleotide polymorphisms (SNPs) and haplotype blocks for asthma genes between Chinese and other populations. The minor allele frequencies for nearly half of our studied SNPs differed by 0.2 or greater between southern Chinese subjects in Hong Kong and European white populations, African populations, or both. Because genome-wide association studies for asthma have not been performed in Chinese subjects, we cannot tell whether the genomic findings of recent consortium-based genome-wide association studies are applicable to our population. In addition, our group performed Roche 454 pyrosequencing on a 100-kb area spanning each of 10 asthma loci in 24 healthy Hong Kong children. For the 17q21 locus, there was substantial variation in the haplotype structures that were constructed from 224 common SNPs among Hong Kong subjects and 6 ethnic groups under the 1000 Genomes Project. Sixteen mostly small haplotype blocks were formed in Hong Kong, whereas 6 haplotype blocks were identified in Han Chinese in Beijing and central European subjects and 11 and 19 blocks were identified in Puerto Rican and Yoruba African subjects. In conclusion, differences in allele frequencies of asthma genes and haplotype structures of asthma loci are found between Chinese subjects and other ethnic groups. These sequence variations must be considered during the selection of tagging SNPs for replicating genetic associations between populations.

摘要

哮喘是由复杂的基因-基因和基因-环境相互作用引起的。大多数哮喘基因在不同人群中不可复制,这可能是由于这些基因的流行病学差异所致。我们的病例对照关联和下一代测序研究揭示了中西方人群哮喘基因中单核苷酸多态性(SNP)和单倍型块的频率存在显著差异。我们研究的 SNP 中,近一半的次要等位基因频率在香港的中国南方人和欧洲白种人、非洲人群或两者之间相差 0.2 或更多。由于尚未在中国人群中进行哮喘全基因组关联研究,我们无法判断最近基于联盟的全基因组关联研究的基因组发现是否适用于我们的人群。此外,我们小组对 24 名香港健康儿童的 10 个哮喘基因座中的每个基因座跨越的 100 kb 区域进行了罗氏 454 焦磷酸测序。对于 17q21 基因座,香港人群和 1000 基因组计划中的 6 个种族群体中的 224 个常见 SNP 构建的单倍型结构存在很大差异。在香港形成了 16 个主要的小单倍型块,而在北京的汉族人群和中欧人群中确定了 6 个单倍型块,在波多黎各和约鲁巴非洲人群中确定了 11 个和 19 个单倍型块。总之,中国人群和其他种族群体之间存在哮喘基因等位基因频率和哮喘基因座单倍型结构的差异。在选择标记 SNP 以复制人群之间的遗传关联时,必须考虑这些序列变异。

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