Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
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
_version_ 1782374561531035648
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
work_keys_str_mv AT weizejun genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT liuyang genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT xuheng genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT tangkun genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT wuhao genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT lulin genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT wangzhe genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT chenzhengjie genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT xujunjie genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT zhuyufei genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT hulandian genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT shanghong genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT zhaoguoping genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations
AT kongxiangyin genomewideassociationstudiesofhiv1hostcontrolinethnicallydiversechinesepopulations