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Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations
Genome-wide association studies (GWASs) have revealed several genetic loci associated with HIV-1 outcome following infection (e.g., HLA-C at 6p21.33) in multi-ethnic populations with genetic heterogeneity and racial/ethnic differences among Caucasians, African-Americans, and Hispanics. To systematic...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4454153/ https://www.ncbi.nlm.nih.gov/pubmed/26039976 http://dx.doi.org/10.1038/srep10879 |
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author | Wei, Zejun Liu, Yang Xu, Heng Tang, Kun Wu, Hao Lu, Lin Wang, Zhe Chen, Zhengjie Xu, Junjie Zhu, Yufei Hu, Landian Shang, Hong Zhao, Guoping Kong, Xiangyin |
author_facet | Wei, Zejun Liu, Yang Xu, Heng Tang, Kun Wu, Hao Lu, Lin Wang, Zhe Chen, Zhengjie Xu, Junjie Zhu, Yufei Hu, Landian Shang, Hong Zhao, Guoping Kong, Xiangyin |
author_sort | Wei, Zejun |
collection | PubMed |
description | Genome-wide association studies (GWASs) have revealed several genetic loci associated with HIV-1 outcome following infection (e.g., HLA-C at 6p21.33) in multi-ethnic populations with genetic heterogeneity and racial/ethnic differences among Caucasians, African-Americans, and Hispanics. To systematically investigate the inherited predisposition to modulate HIV-1 infection in Chinese populations, we performed GWASs in three ethnically diverse HIV-infected patients groups (i.e., HAN, YUN, and XIN, N = 538). The reported loci at 6p21.33 was validated in HAN (e.g., rs9264942, P = 0.0018). An independent association signal (rs2442719, P = 7.85 × 10(−7), HAN group) in the same region was observed. Imputation results suggest that haplotype HLA-B*13:02/C*06:02, which can partially account for the GWAS signal, is associated with lower viral load in Han Chinese. Moreover, several novel loci were identified using GWAS approach including the top association signals at 6q13 (KCNQ5, rs947612, P = 2.15 × 10(−6)), 6p24.1 (PHACTR1, rs202072, P = 3.8 × 10(−6)), and 11q12.3 (SCGB1D4, rs11231017, P = 7.39 × 10(−7)) in HAN, YUN, and XIN groups, respectively. Our findings imply shared or specific mechanisms for host control of HIV-1 in ethnically diverse Chinese populations, which may shed new light on individualized HIV/AIDS therapy in China. |
format | Online Article Text |
id | pubmed-4454153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44541532015-06-10 Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations Wei, Zejun Liu, Yang Xu, Heng Tang, Kun Wu, Hao Lu, Lin Wang, Zhe Chen, Zhengjie Xu, Junjie Zhu, Yufei Hu, Landian Shang, Hong Zhao, Guoping Kong, Xiangyin Sci Rep Article Genome-wide association studies (GWASs) have revealed several genetic loci associated with HIV-1 outcome following infection (e.g., HLA-C at 6p21.33) in multi-ethnic populations with genetic heterogeneity and racial/ethnic differences among Caucasians, African-Americans, and Hispanics. To systematically investigate the inherited predisposition to modulate HIV-1 infection in Chinese populations, we performed GWASs in three ethnically diverse HIV-infected patients groups (i.e., HAN, YUN, and XIN, N = 538). The reported loci at 6p21.33 was validated in HAN (e.g., rs9264942, P = 0.0018). An independent association signal (rs2442719, P = 7.85 × 10(−7), HAN group) in the same region was observed. Imputation results suggest that haplotype HLA-B*13:02/C*06:02, which can partially account for the GWAS signal, is associated with lower viral load in Han Chinese. Moreover, several novel loci were identified using GWAS approach including the top association signals at 6q13 (KCNQ5, rs947612, P = 2.15 × 10(−6)), 6p24.1 (PHACTR1, rs202072, P = 3.8 × 10(−6)), and 11q12.3 (SCGB1D4, rs11231017, P = 7.39 × 10(−7)) in HAN, YUN, and XIN groups, respectively. Our findings imply shared or specific mechanisms for host control of HIV-1 in ethnically diverse Chinese populations, which may shed new light on individualized HIV/AIDS therapy in China. Nature Publishing Group 2015-06-03 /pmc/articles/PMC4454153/ /pubmed/26039976 http://dx.doi.org/10.1038/srep10879 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wei, Zejun Liu, Yang Xu, Heng Tang, Kun Wu, Hao Lu, Lin Wang, Zhe Chen, Zhengjie Xu, Junjie Zhu, Yufei Hu, Landian Shang, Hong Zhao, Guoping Kong, Xiangyin Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations |
title | Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations |
title_full | Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations |
title_fullStr | Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations |
title_full_unstemmed | Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations |
title_short | Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations |
title_sort | genome-wide association studies of hiv-1 host control in ethnically diverse chinese populations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4454153/ https://www.ncbi.nlm.nih.gov/pubmed/26039976 http://dx.doi.org/10.1038/srep10879 |
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