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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2018
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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. |
format | Online Article Text |
id | pubmed-6023959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
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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