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Zinc-Finger Nucleases Induced by HIV-1 Tat Excise HIV-1 from the Host Genome in Infected and Latently Infected Cells

Highly active anti-retroviral therapy (HAART) cannot clear infected cells harboring HIV-1 proviral DNA from HIV-1-infected patients. We previously demonstrated that zinc-finger nucleases (ZFNs) can specifically and efficiently excise HIV-1 proviral DNA from latently infected human T cells by targeti...

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Autores principales: Ji, Haiyan, Lu, Panpan, Liu, Baochi, Qu, Xiying, Wang, Yanan, Jiang, Zhengtao, Yang, Xinyi, Zhong, Yangcheng, Yang, He, Pan, Hanyu, Zhao, Lin, Xu, Jianqing, Lu, Hongzhou, Zhu, Huanzhang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023959/
https://www.ncbi.nlm.nih.gov/pubmed/30195798
http://dx.doi.org/10.1016/j.omtn.2018.04.014
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author Ji, Haiyan
Lu, Panpan
Liu, Baochi
Qu, Xiying
Wang, Yanan
Jiang, Zhengtao
Yang, Xinyi
Zhong, Yangcheng
Yang, He
Pan, Hanyu
Zhao, Lin
Xu, Jianqing
Lu, Hongzhou
Zhu, Huanzhang
author_facet Ji, Haiyan
Lu, Panpan
Liu, Baochi
Qu, Xiying
Wang, Yanan
Jiang, Zhengtao
Yang, Xinyi
Zhong, Yangcheng
Yang, He
Pan, Hanyu
Zhao, Lin
Xu, Jianqing
Lu, Hongzhou
Zhu, Huanzhang
author_sort Ji, Haiyan
collection PubMed
description Highly active anti-retroviral therapy (HAART) cannot clear infected cells harboring HIV-1 proviral DNA from HIV-1-infected patients. We previously demonstrated that zinc-finger nucleases (ZFNs) can specifically and efficiently excise HIV-1 proviral DNA from latently infected human T cells by targeting long terminal repeats (LTRs), a novel and alternative antiretroviral strategy for eradicating HIV-1 infection. To prevent unwanted off-target effects from constantly expressed ZFNs, in this study, we engineered the expression of ZFNs under the control of HIV-1 LTR, by which ZFN expression can be activated by the HIV-1 (Trans-Activator of Transcription) Tat protein. Our results show that functional expression of ZFNs induced by Tat excise the integrated proviral DNA of HIV-NL4-3-eGFP in approximately 30% of the population of HIV-1-infected cells. The results from HIV-1-infected human primary T cells and latently infected T cells treated with the inducible ZFNs further validated that proviral DNA can be excised. Taken together, positively regulated expression of ZFNs in the presence of HIV-1 Tat may provide a safer and novel implementation of genome-editing technology for eradicating HIV-1 proviral DNA from infected host cells.
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spelling pubmed-60239592018-06-29 Zinc-Finger Nucleases Induced by HIV-1 Tat Excise HIV-1 from the Host Genome in Infected and Latently Infected Cells Ji, Haiyan Lu, Panpan Liu, Baochi Qu, Xiying Wang, Yanan Jiang, Zhengtao Yang, Xinyi Zhong, Yangcheng Yang, He Pan, Hanyu Zhao, Lin Xu, Jianqing Lu, Hongzhou Zhu, Huanzhang Mol Ther Nucleic Acids Article Highly active anti-retroviral therapy (HAART) cannot clear infected cells harboring HIV-1 proviral DNA from HIV-1-infected patients. We previously demonstrated that zinc-finger nucleases (ZFNs) can specifically and efficiently excise HIV-1 proviral DNA from latently infected human T cells by targeting long terminal repeats (LTRs), a novel and alternative antiretroviral strategy for eradicating HIV-1 infection. To prevent unwanted off-target effects from constantly expressed ZFNs, in this study, we engineered the expression of ZFNs under the control of HIV-1 LTR, by which ZFN expression can be activated by the HIV-1 (Trans-Activator of Transcription) Tat protein. Our results show that functional expression of ZFNs induced by Tat excise the integrated proviral DNA of HIV-NL4-3-eGFP in approximately 30% of the population of HIV-1-infected cells. The results from HIV-1-infected human primary T cells and latently infected T cells treated with the inducible ZFNs further validated that proviral DNA can be excised. Taken together, positively regulated expression of ZFNs in the presence of HIV-1 Tat may provide a safer and novel implementation of genome-editing technology for eradicating HIV-1 proviral DNA from infected host cells. American Society of Gene & Cell Therapy 2018-05-03 /pmc/articles/PMC6023959/ /pubmed/30195798 http://dx.doi.org/10.1016/j.omtn.2018.04.014 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Ji, Haiyan
Lu, Panpan
Liu, Baochi
Qu, Xiying
Wang, Yanan
Jiang, Zhengtao
Yang, Xinyi
Zhong, Yangcheng
Yang, He
Pan, Hanyu
Zhao, Lin
Xu, Jianqing
Lu, Hongzhou
Zhu, Huanzhang
Zinc-Finger Nucleases Induced by HIV-1 Tat Excise HIV-1 from the Host Genome in Infected and Latently Infected Cells
title Zinc-Finger Nucleases Induced by HIV-1 Tat Excise HIV-1 from the Host Genome in Infected and Latently Infected Cells
title_full Zinc-Finger Nucleases Induced by HIV-1 Tat Excise HIV-1 from the Host Genome in Infected and Latently Infected Cells
title_fullStr Zinc-Finger Nucleases Induced by HIV-1 Tat Excise HIV-1 from the Host Genome in Infected and Latently Infected Cells
title_full_unstemmed Zinc-Finger Nucleases Induced by HIV-1 Tat Excise HIV-1 from the Host Genome in Infected and Latently Infected Cells
title_short Zinc-Finger Nucleases Induced by HIV-1 Tat Excise HIV-1 from the Host Genome in Infected and Latently Infected Cells
title_sort zinc-finger nucleases induced by hiv-1 tat excise hiv-1 from the host genome in infected and latently infected cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023959/
https://www.ncbi.nlm.nih.gov/pubmed/30195798
http://dx.doi.org/10.1016/j.omtn.2018.04.014
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