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利用多向混合映射阐明南非有色人种群体中的结核病易感性。

Using multi-way admixture mapping to elucidate TB susceptibility in the South African Coloured population.

作者信息

Daya Michelle, van der Merwe Lize, Gignoux Christopher R, van Helden Paul D, Möller Marlo, Hoal Eileen G

机构信息

Molecular Biology and Human Genetics, MRC Centre for TB Research and the DST/NRF Centre of Excellence for Biomedical TB Research, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.

出版信息

BMC Genomics. 2014 Nov 25;15(1):1021. doi: 10.1186/1471-2164-15-1021.

Abstract

BACKGROUND

The admixed South African Coloured population is ideally suited to the discovery of tuberculosis susceptibility genetic variants and their probable ethnic origins, but previous attempts at finding such variants using genome-wide admixture mapping were hampered by the inaccuracy of local ancestry inference. In this study, we infer local ancestry using the novel algorithm implemented in RFMix, with the emphasis on identifying regions of excess San or Bantu ancestry, which we hypothesize may harbour TB susceptibility genes.

RESULTS

Using simulated data, we demonstrate reasonable accuracy of local ancestry inference by RFMix, with a tendency towards miss-calling San ancestry as Bantu. Regions with either excess San ancestry or excess African (San or Bantu) ancestry are less likely to be affected by this bias, and we therefore proceeded to identify such regions, found in cases but not in controls (642 cases and 91 controls). A number of promising regions were found (overall p-values of 7.19×10-5 for San ancestry and <2.00×10-16 for African ancestry), including chromosomes 15q15 and 17q22, which are close to genomic regions previously implicated in TB. Promising immune-related susceptibility genes such as the GADD45A, OSM and B7-H5 genes are also harboured in the identified regions.

CONCLUSION

Admixture mapping is feasible in the South African Coloured population and a number of novel TB susceptibility genomic regions were uncovered.

摘要

背景

南非混血有色人种非常适合用于发现结核病易感性基因变异及其可能的种族起源,但先前利用全基因组混合映射寻找此类变异的尝试因本地祖先推断的不准确而受阻。在本研究中,我们使用RFMix中实现的新算法推断本地祖先,重点是识别具有过多桑人或班图人祖先的区域,我们假设这些区域可能含有结核病易感基因。

结果

使用模拟数据,我们证明了RFMix在本地祖先推断方面具有合理的准确性,存在将桑人祖先误判为班图人祖先的倾向。具有过多桑人祖先或过多非洲(桑人或班图人)祖先的区域受此偏差影响的可能性较小,因此我们继续识别此类区域,这些区域在病例中发现而在对照中未发现(642例病例和91例对照)。发现了一些有前景的区域(桑人祖先的总体p值为7.19×10-5,非洲祖先的总体p值<2.00×10-16),包括15q15和17q22染色体,它们靠近先前与结核病相关的基因组区域。在识别出的区域中还含有一些有前景的免疫相关易感基因,如GADD45A、OSM和B7-H5基因。

结论

混合映射在南非有色人种中是可行的,并且发现了一些新的结核病易感性基因组区域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed7/4256931/0bf7278dbde9/12864_2014_6716_Fig1_HTML.jpg

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