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Ring finger protein 39 genetic variants associate with HIV-1 plasma viral loads and its replication in cell culture

BACKGROUND: The human immunodeficiency virus (HIV-1) exploits host proteins to complete its life cycle. Genome-wide siRNA approaches suggested that host proteins affect HIV-1 replication. However, the results barely overlapped. RING finger protein 39 (RNF39) has been identified from genome-wide asso...

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Autores principales: Lin, Ying-Ju, Chen, Chia-Yen, Jeang, Kuan-Teh, Liu, Xiang, Wang, Jen-Hsien, Hung, Chien-Hui, Tsang, Hsinyi, Lin, Ting-Hsu, Liao, Chiu-Chu, Huang, Shao-Mei, Lin, Cheng-Wen, Ho, Mao-Wang, Chien, Wen-Kuei, Chen, Jin-Hua, Ho, Tsung-Jung, Tsai, Fuu-Jen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131809/
https://www.ncbi.nlm.nih.gov/pubmed/25126410
http://dx.doi.org/10.1186/2045-3701-4-40
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author Lin, Ying-Ju
Chen, Chia-Yen
Jeang, Kuan-Teh
Liu, Xiang
Wang, Jen-Hsien
Hung, Chien-Hui
Tsang, Hsinyi
Lin, Ting-Hsu
Liao, Chiu-Chu
Huang, Shao-Mei
Lin, Cheng-Wen
Ho, Mao-Wang
Chien, Wen-Kuei
Chen, Jin-Hua
Ho, Tsung-Jung
Tsai, Fuu-Jen
author_facet Lin, Ying-Ju
Chen, Chia-Yen
Jeang, Kuan-Teh
Liu, Xiang
Wang, Jen-Hsien
Hung, Chien-Hui
Tsang, Hsinyi
Lin, Ting-Hsu
Liao, Chiu-Chu
Huang, Shao-Mei
Lin, Cheng-Wen
Ho, Mao-Wang
Chien, Wen-Kuei
Chen, Jin-Hua
Ho, Tsung-Jung
Tsai, Fuu-Jen
author_sort Lin, Ying-Ju
collection PubMed
description BACKGROUND: The human immunodeficiency virus (HIV-1) exploits host proteins to complete its life cycle. Genome-wide siRNA approaches suggested that host proteins affect HIV-1 replication. However, the results barely overlapped. RING finger protein 39 (RNF39) has been identified from genome-wide association studies. However, its function during HIV-1 replication remains unclear. METHODS AND RESULTS: We investigated the relationship between common RNF39 genetic variants and HIV-1 viral loads. The effect of RNF39 protein knockdown or overexpression on HIV-1 replication was then investigated in different cell lines. Two genetic variants were associated with HIV-1 viral loads. Patients with the ht1-GG/GG haplotype presented lower RNF39 expression levels and lower HIV-1 viral load. RNF39 knockdown inhibited HIV-1 expression. CONCLUSIONS: RNF39 protein may be involved in HIV-1 replication as observed in genetic studies on patients with HIV-1 and in in vitro cell cultures.
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spelling pubmed-41318092014-08-15 Ring finger protein 39 genetic variants associate with HIV-1 plasma viral loads and its replication in cell culture Lin, Ying-Ju Chen, Chia-Yen Jeang, Kuan-Teh Liu, Xiang Wang, Jen-Hsien Hung, Chien-Hui Tsang, Hsinyi Lin, Ting-Hsu Liao, Chiu-Chu Huang, Shao-Mei Lin, Cheng-Wen Ho, Mao-Wang Chien, Wen-Kuei Chen, Jin-Hua Ho, Tsung-Jung Tsai, Fuu-Jen Cell Biosci Research BACKGROUND: The human immunodeficiency virus (HIV-1) exploits host proteins to complete its life cycle. Genome-wide siRNA approaches suggested that host proteins affect HIV-1 replication. However, the results barely overlapped. RING finger protein 39 (RNF39) has been identified from genome-wide association studies. However, its function during HIV-1 replication remains unclear. METHODS AND RESULTS: We investigated the relationship between common RNF39 genetic variants and HIV-1 viral loads. The effect of RNF39 protein knockdown or overexpression on HIV-1 replication was then investigated in different cell lines. Two genetic variants were associated with HIV-1 viral loads. Patients with the ht1-GG/GG haplotype presented lower RNF39 expression levels and lower HIV-1 viral load. RNF39 knockdown inhibited HIV-1 expression. CONCLUSIONS: RNF39 protein may be involved in HIV-1 replication as observed in genetic studies on patients with HIV-1 and in in vitro cell cultures. BioMed Central 2014-08-05 /pmc/articles/PMC4131809/ /pubmed/25126410 http://dx.doi.org/10.1186/2045-3701-4-40 Text en Copyright © 2014 Lin et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lin, Ying-Ju
Chen, Chia-Yen
Jeang, Kuan-Teh
Liu, Xiang
Wang, Jen-Hsien
Hung, Chien-Hui
Tsang, Hsinyi
Lin, Ting-Hsu
Liao, Chiu-Chu
Huang, Shao-Mei
Lin, Cheng-Wen
Ho, Mao-Wang
Chien, Wen-Kuei
Chen, Jin-Hua
Ho, Tsung-Jung
Tsai, Fuu-Jen
Ring finger protein 39 genetic variants associate with HIV-1 plasma viral loads and its replication in cell culture
title Ring finger protein 39 genetic variants associate with HIV-1 plasma viral loads and its replication in cell culture
title_full Ring finger protein 39 genetic variants associate with HIV-1 plasma viral loads and its replication in cell culture
title_fullStr Ring finger protein 39 genetic variants associate with HIV-1 plasma viral loads and its replication in cell culture
title_full_unstemmed Ring finger protein 39 genetic variants associate with HIV-1 plasma viral loads and its replication in cell culture
title_short Ring finger protein 39 genetic variants associate with HIV-1 plasma viral loads and its replication in cell culture
title_sort ring finger protein 39 genetic variants associate with hiv-1 plasma viral loads and its replication in cell culture
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131809/
https://www.ncbi.nlm.nih.gov/pubmed/25126410
http://dx.doi.org/10.1186/2045-3701-4-40
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