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The site of HIV-1 integration in the human genome determines basal transcriptional activity and response to Tat transactivation
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Because of the heterogeneity of chromatin, the site of integration of human immunodeficiency virus (HIV) in the genome could have dramatic effects on its transcriptional activity. We have used an HIV-1-derived retroviral vector, in which the green fluorescent protein is under the control of the HIV promoter, to generate by infection 34 Jurkat clonal cell lines each containing a single integration of the HIV-1 vector. In the absence of Tat, a 75-fold difference in expression level between the highest and lowest expressing clones was observed. Basal promoter activity was low in 80% of the clones and moderate to high in the remaining 20% of clones. We found that differences in expression levels are due to the integration site and are not controlled by DNA methylation or histone acetylation. Tat activated transcription in each clone, and an inverse correlation was observed between basal transcriptional activity and inducibility by Tat. These observations demonstrate that the chromatin environment influences basal HIV gene expression and that the HIV Tat protein activates transcription independently of the chromatin environment.
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“However, it is now becoming clearer that certain retroviruses like HIV tend to target gene-rich, transcriptionally active, euchromatic regions within the host’s chromosome to integrate.”
From Beyond reverse transcription: molecular mechanisms and emerging paradigms in retroviral replication (2026) · cites this paper as Jordan et al. 2001
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“For example, proviral integration in the transcriptionally active regions could potentially favor expression of the viral genes, whereas integration in the transcriptionally silent regions (heterochromatin) may not be in favor of viral expression and may even force the virus to stay transcriptionally silent (Jordan et al. 2001, Lewinski et al. 2006, Einkauf et al. 2022, Teixeira et al. 2024).”
From Beyond reverse transcription: molecular mechanisms and emerging paradigms in retroviral replication (2026) · cites this paper as Jordan et al. 2001
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A Third-Generation Lentivirus Vector with a Conditional Packaging System
Dull, T., Zufferey, R., Kelly, M., Mandel, R. J., Nguyen, M., Trono, D., & Naldini, L. (1998) · Journal of Virology · doi:10.1128/jvi.72.11.8463-8471.1998 · Cited by 3,341
Dissecting the regulatory circuitry of a eukaryotic genome
Holstege, F. C. P., Jennings, E. G., Wyrick, J. J., Lee, T. I., Hengartner, C. J., Green, M. R., Golub, T. R., Lander, E. S., & Young, R. A. (1998) · Cell · doi:10.1016/s0092-8674(00)81641-4 · Cited by 1,670
Ory, D., Neugeboren, B. I., & Mulligan, R. C. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11400 · Cited by 926
Anti-termination of transcription within the long terminal repeat of HIV-1 by tat gene product
Kao, S.-Y., Calman, A. F., Luciw, P. A., & Peterlin, B. M. (1987) · Nature · doi:10.1038/330489a0 · Cited by 908
HIV-1 Genome Nuclear Import Is Mediated by a Central DNA Flap
Zennou, V., Petit, C., Guétard, D., Nerhbass, U., Montagnier, L., & Charneau, P. (2000) · Cell · doi:10.1016/s0092-8674(00)80828-4 · Cited by 864
Miller, M. D., Farnet, C. M., & Bushman, F. D. (1997) · Journal of Virology · doi:10.1128/jvi.71.7.5382-5390.1997 · Cited by 620
Lint, C. M. V., Emiliani, S., Ott, M., & Verdin, E. M. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00449.x · Cited by 579
Self-citationP-TEFb kinase is required for HIV Tat transcriptional activation in vivo and in vitroPreprint
Mancebo, H. S. Y., Lee, G., Flygare, J. A., Tomassini, J. E., Luu, P., Zhu, Y., Peng, J., Blau, C., Hazuda, D. J., Price, D. H., et al. (1997) · Genes & Development · doi:10.1101/gad.11.20.2633 · Cited by 546
Binding and Stimulation of HIV-1 Integrase by a Human Homolog of Yeast Transcription Factor SNF5
Kalpana, G. V., Marmon, S., Wang, W., Crabtree, G. R., & Goff, S. P. (1994) · Science · doi:10.1126/science.7801128 · Cited by 530
Verdin, E. M., Paras, P., & Lint, C. M. V. (1993) · The EMBO Journal · doi:10.1002/j.1460-2075.1993.tb05994.x · Cited by 520
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Waddington, S. N., Mitrophanous, K. A., Ellard, F. M., Buckley, S. M. K., Nivsarkar, M. S., Lawrence, L., Cook, H. T., Al-Allaf, F. A., Bigger, B., Kingsman, S. M., et al. (2003) · Gene Therapy · doi:10.1038/sj.gt.3301991 · Cited by 78
Witte, A. V., Laffert, B., Rosorius, O., Lischka, P., Blume, K., Galler, G. R., Stilper, A., Willbold, D., D’Aloja, P., Sixt, M., et al. (2004) · Molecular Cell · doi:10.1016/s1097-2765(04)00004-8 · Cited by 79
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Sung, T.-L., & Rice, A. P. (2006) · Retrovirology · doi:10.1186/1742-4690-3-66 · Cited by 74
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Dieudonné, M., Maiuri, P., Biancotto, C., Knezevich, A., Kula, A., Lušić, M., & Marcello, A. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.141 · Cited by 77
Demeulemeester, J., De Rijck, J., Gijsbers, R., & Debyser, Z. (2015) · BioEssays · doi:10.1002/bies.201500051 · Cited by 71
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Gallo, R. C. (2002) · Immunological Reviews · doi:10.1034/j.1600-065x.2002.18520.x · Cited by 69
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Lu, P., Qu, X., Shen, Y., Jiang, Z., Wang, P., Zeng, H., Ji, H., Deng, J., Yang, X., Li, X., et al. (2016) · Scientific Reports · doi:10.1038/srep24100 · Cited by 66
HIV-1 regulation of latency in the monocyte-macrophage lineage and in CD4+ T lymphocytes
Redel, L., Douce, V. L., Cherrier, T., Marban, C., Janossy, A., Aunis, D., Lint, C. M. V., Rohr, O., & Schwartz, C. (2009) · Journal of Leukocyte Biology · doi:10.1189/jlb.0409264 · Cited by 74
Leonard, J. N., & Schaffer, D. V. (2005) · Journal of Virology · doi:10.1128/jvi.79.3.1645-1654.2005 · Cited by 66
Trejbalová, K., Kovářová, D., Blažková, J., Machala, L., Jilich, D., Weber, J., Kučerová, D., Vencálek, O., Hirsch, I., & Hejnar, J. (2016) · Clinical Epigenetics · doi:10.1186/s13148-016-0185-6 · Cited by 67
Lost in Transcription: Molecular Mechanisms that Control HIV Latency
Taube, R., & Peterlin, B. M. (2013) · Viruses · doi:10.3390/v5030902 · Cited by 63
Saito, A., Henning, M. S., Serrao, E., Dubose, B. N., Teng, S., Huang, J., Li, X., Saito, N., Roy, S. P., Siddiqui, M. A., et al. (2016) · Journal of Virology · doi:10.1128/jvi.00019-16 · Cited by 61
Varying virulence: epigenetic control of expression noise and disease processes
Miller‐Jensen, K., Dey, S. S., Schaffer, D. V., & Arkin, A. P. (2011) · Trends in biotechnology · doi:10.1016/j.tibtech.2011.05.004 · Cited by 62
Kakizoe, Y., Nakaoka, S., Beauchemin, C. A. A., Morita, S., Mori, H., Igarashi, T., Aihara, K., Miura, T., & Iwami, S. (2015) · Scientific Reports · doi:10.1038/srep10371 · Cited by 63
Ho, S. C. L., Mariati, Yeo, J. H. M., Fang, S. G., & Yang, Y. (2014) · Molecular Biotechnology · doi:10.1007/s12033-014-9809-2 · Cited by 62
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Margolis, D. M., & Archin, N. M. (2016) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiw618 · Cited by 62
Ding, D., Qu, X., Li, L., Zhou, X., Liu, S., Lin, S., Wang, P., Liu, S., Kong, C., Wang, X., et al. (2013) · Virology · doi:10.1016/j.virol.2013.02.022 · Cited by 60
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Easley, R. L., Duyne, R. V., Coley, W., Guendel, I., Dadgar, S., Kehn‐Hall, K., & Kashanchi, F. (2009) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2009.08.008 · Cited by 58
Telwatte, S., Morón‐López, S., Aran, D., Kim, P., Hsieh, C. L., Joshi, S. K., Montaño, M., Greene, W. C., Butte, A. J., Wong, J. K., et al. (2019) · Retrovirology · doi:10.1186/s12977-019-0494-x · Cited by 60
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Gatignol, A. (2007) · Advances in pharmacology · doi:10.1016/s1054-3589(07)55004-0 · Cited by 70
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Abner, E., Stoszko, M., Zeng, L., Chen, H., Izquierdo‐Bouldstridge, A., Konuma, T., Zorita, E. V., Fanunza, E., Zhang, Q., Mahmoudi, T., et al. (2018) · Journal of Virology · doi:10.1128/jvi.02056-17 · Cited by 54
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The Molecular Biology of HIV Latency
Khoury, G., Darcis, G., Lee, M. Y.-H., Bouchat, S., Driessche, B. V., Purcell, D. F. J., & Lint, C. M. V. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-0484-2_8 · Cited by 55
Pion, M., Jordan, A., Biancotto, A., Dequiedt, F., Gondois‐Rey, F., Rondeau, S., Vigne, R., Hejnar, J., Verdin, E. M., & Hirsch, I. (2003) · Journal of Virology · doi:10.1128/jvi.77.7.4025-4032.2003 · Cited by 56
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Vatakis, D. N., Kim, S., Kim, N., Chow, S. A., & Zack, J. A. (2009) · Journal of Virology · doi:10.1128/jvi.00356-09 · Cited by 52
Sunshine, S., Kirchner, R., Amr, S. S., Mansur, L., Shakhbatyan, R., Kim, M., Bosque, A., Siliciano, R. F., Planelles, V., Hofmann, O., et al. (2016) · Journal of Virology · doi:10.1128/jvi.01617-15 · Cited by 54
Endo, M., Zoltick, P. W., Peranteau, W. H., Radu, A. P., Muvarak, N. E., Ito, M., Yang, Z., Cotsarelis, G., & Flake, A. W. (2007) · Molecular Therapy · doi:10.1038/sj.mt.6300332 · Cited by 52
Rev-dependent lentiviral expression vector
Wu, Y., Beddall, M. H., & Marsh, J. W. (2007) · Retrovirology · doi:10.1186/1742-4690-4-12 · Cited by 52
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Maroun, M., Delelis, O., Coadou, G., Bader, T., Ségéral, E., Mbemba, G., Petit, C., Sonigo, P., Rain, J., Mouscadet, J. F., et al. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m604849200 · Cited by 52
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Jeeninga, R. E., Westerhout, E. M., van Gerven, M. L., & Berkhout, B. (2008) · Retrovirology · doi:10.1186/1742-4690-5-37 · Cited by 52
Boullé, M., Müller, T. G., Dähling, S., Ganga, Y., Jackson, L., Mahamed, D., Lance, O., Lustig, G., Neher, R. A., & Sigal, A. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005964 · Cited by 52
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MacNeil, A., Sankalé, J.-L., Meloni, S., Sarr, A. D., Mboup, S., & Kanki, P. J. (2006) · Journal of Virology · doi:10.1128/jvi.00604-06 · Cited by 51
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Malcolm, T., Chen, J., Chang, C., & Sadowski, I. (2007) · Virus Genes · doi:10.1007/s11262-007-0109-9 · Cited by 49
Gérard, A., Ségéral, E., Naughtin, M., Abdouni, A., Muylder, B. C.-D., Cheynier, R., Rain, J., & Emiliani, S. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2014.12.002 · Cited by 61
Liu, Q., Li, W., Huang, L., Asada, Y., Morris-Natschke, S. L., Chen, C., Lee, K., & Koike, K. (2018) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2018.07.020 · Cited by 49
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Wu, Y., & Marsh, J. W. (2003) · Microbes and Infection · doi:10.1016/s1286-4579(03)00187-4 · Cited by 47
Mauldin, K., Sharma, A., Awasthi, S., Matlock, E. F., Rogers, L., Lint, C. M. V., Skiest, D. J., Burns, D. K., & Harrod, R. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m408643200 · Cited by 46
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Gray, L. R., Cowley, D., Welsh, C., Lu, H. K., Brew, B. J., Lewin, S. R., Wesselingh, S. L., Gorry, P. R., & Churchill, M. J. (2015) · Molecular Psychiatry · doi:10.1038/mp.2015.111 · Cited by 43
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Martínez‐Bonet, M., Clemente, M. I., Serramía, M. J., Muñóz, E., Moreno, S., & Muñoz‐Fernández, M. Á. (2015) · Scientific Reports · doi:10.1038/srep16445 · Cited by 43
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Naamati, A., Williamson, J. C., Greenwood, E. J. D., Marelli, S., Lehner, P. J., & Matheson, N. J. (2019) · eLife · doi:10.7554/elife.41431 · Cited by 44
Wonderlich, E. R., Subramanian, K., Cox, B. D., Wiegand, A. P., Lackman-Smith, C., Bale, M. J., Stone, M., Hoh, R., Kearney, M. F., Maldarelli, F. M., et al. (2019) · PLoS Pathogens · doi:10.1371/journal.ppat.1008074 · Cited by 43
Molecular mechanisms of HIV-1 proviral latency
Bisgrove, D. A., Lewinski, M. K., Bushman, F. D., & Verdin, E. M. (2005) · Expert Review of Anti-infective Therapy · doi:10.1586/14787210.3.5.805 · Cited by 42
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Cereseto, A., & Giacca, M. (2004) · PubMed · Cited by 43
Mechanisms of HIV transcriptional regulation by drugs of abuse
Tyagi, M., Bukrinsky, M., & L. Simon, G. (2016) · Current HIV Research · doi:10.2174/1570162x14666160324124736 · Cited by 42
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Swindle, C. S., & Klug, C. A. (2002) · Stem Cells and Development · doi:10.1089/15258160260090915 · Cited by 41
Albert, B. J., Niu, A., Ramani, R., Marshall, G. R., Wender, P. A., Williams, R. M., Ratner, L., Barnes, A. B., & Kyei, G. B. (2017) · Scientific Reports · doi:10.1038/s41598-017-07814-4 · Cited by 42
Elleder, D., Pavlı́ček, A., Pačes, J., & Hejnar, J. (2002) · FEBS Letters · doi:10.1016/s0014-5793(02)02612-1 · Cited by 41
Quivy, V., & Lint, C. M. V. (2002) · Biochemical Pharmacology · doi:10.1016/s0006-2952(02)01152-8 · Cited by 40
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Mahmoudi, T. (2012) · Transcription · doi:10.4161/trns.20541 · Cited by 41
Debyser, Z., Vansant, G., Bruggemans, A., Janssens, J., & Christ, F. (2018) · Viruses · doi:10.3390/v11010012 · Cited by 41
Cao, S., Slack, S. D., Levy, C., Hughes, S. M., Jiang, Y., Yogodzinski, C., Roychoudhury, P., Jerome, K. R., Schiffer, J. T., Hladik, F., et al. (2019) · Science Advances · doi:10.1126/sciadv.aav6322 · Cited by 39
Dahabieh, M. S., Ooms, M., Brumme, C. J., Taylor, J. M. G., Harrigan, P. R., Simon, V. R., & Sadowski, I. (2014) · Retrovirology · doi:10.1186/1742-4690-11-17 · Cited by 41
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Irwan, I. D., Bogerd, H. P., & Cullen, B. R. (2022) · Nature Microbiology · doi:10.1038/s41564-022-01264-z · Cited by 39
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Lange, U. C., Verdikt, R., Aït-Ammar, A., & Lint, C. M. V. (2020) · Seminars in Immunopathology · doi:10.1007/s00281-020-00783-3 · Cited by 41
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Yang, X., Wang, Y., Lu, P., Shen, Y., Zhao, X., Zhu, Y., Jiang, Z., Yang, H. B., Pan, H., Zhao, L., et al. (2020) · EMBO Reports · doi:10.15252/embr.201949305 · Cited by 39
Mok, H. P., Javed, S., & Lever, A. M. L. (2007) · Gene Therapy · doi:10.1038/sj.gt.3302923 · Cited by 44
Ying, H., Zhang, Y., Zhou, X., Qu, X., Wang, P., Liu, S., Lu, D., & Zhu, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048832 · Cited by 38
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Day, T., & Kublin, J. G. (2014) · Current HIV Research · doi:10.2174/1570162x113116660051 · Cited by 37
Matsuda, K., Kobayakawa, T., Tsuchiya, K., Hattori, S.-I., Nomura, W., Gatanaga, H., Yoshimura, K., Oka, S., Endo, Y., Tamamura, H., et al. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.005798 · Cited by 36
Iyer, S. R., Yu, D., Biancotto, A., Margolis, L. B., & Wu, Y. (2009) · Journal of Virology · doi:10.1128/jvi.00874-09 · Cited by 37
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Sadowski, I., & Mitchell, D. A. (2005) · European Journal of Cancer · doi:10.1016/j.ejca.2005.08.011 · Cited by 34
Nunzio, F. D. (2013) · Virus Research · doi:10.1016/j.virusres.2013.09.003 · Cited by 43
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Quivy, V., de Walque, S., & Lint, C. M. V. (2007) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/1-4020-5466-1_17 · Cited by 36
Miller‐Jensen, K., Skupsky, R., Shah, P. S., Arkin, A. P., & Schaffer, D. V. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003135 · Cited by 36
Katz, R. A., Jack-Scott, E., Narezkina, A., Palagin, I. S., Boimel, P. J., Kulkosky, J., Nicolas, É., Greger, J., & Skalka, A. M. (2007) · Journal of Virology · doi:10.1128/jvi.01643-06 · Cited by 36
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Mok, H. P., & Lever, A. M. L. (2007) · Genome biology · doi:10.1186/gb-2007-8-11-228 · Cited by 38
Armani-Tourret, M., Gao, C., Hartana, C. A., Sun, W., Carrere, L., Vela, L., Hochroth, A., Bellefroid, M., Sbrolla, A., Shea, K., et al. (2024) · Cell · doi:10.1016/j.cell.2024.01.037 · Cited by 37
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Brogdon, J. M., Ziani, W., Wang, X., Veazey, R. S., & Xu, H. (2016) · Scientific Reports · doi:10.1038/srep39032 · Cited by 34
Winans, S., & Goff, S. P. (2020) · PLOS Pathogens · doi:10.1371/journal.ppat.1009147 · Cited by 29
Yeo, J. H. M., Ho, S. C. L., Mariati, M., Koh, E. Y. C., Tay, S. J., Woen, S., Zhang, P., & Yang, Y. (2017) · Biotechnology Journal · doi:10.1002/biot.201700175 · Cited by 36
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Kutsch, O., Levy, D. N., Bates, P. J., Decker, J. M., Kosloff, B. R., Shaw, G. M., Priebe, W., & Benveniste, E. N. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.48.5.1652-1663.2004 · Cited by 34
Metadata
- Authors
- Jordan, A., Defechereux, P., & Verdin, E.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Verdin, Eric
- Venue
- The EMBO Journal
- Published
- 2001-04-02
- Volume
- 20
- Issue
- 7
- Pages
- 1726-1738
- ISSN
- 0261-4189 (ISSN-L)
- 1460-2075
- PMC
- PMC145503
- OpenAlex
- W1964660012
- Cited by
- 467
- References
- 48
- Citations by year
- 2026: 13 · 2025: 21 · 2024: 19 · 2023: 18 · 2022: 15 · 2021: 15 · 2020: 21 · 2019: 21 · 2018: 20 · 2017: 26 · 2016: 25 · 2015: 27 · 2014: 14 · 2013: 15 · 2012: 14
- FWCI
- 6.25
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The EMBO Journal (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Belgian American Educational Foundation
- National Institutes of Health
- National Institute of General Medical Sciences (GM51671-05A2, R01GM051671)
- Topics
- Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- Tat transactivation, basal transcription, chromatin environment, HIV-1 promoter, retroviral vectors, Jurkat cells, DNA methylation, histone acetylation, HIV gene expression
- MeSH terms
- Binding Sites, Cell Line, Transformed, Genetic Vectors, HeLa Cells, Humans, Hydroxamic Acids, Promoter Regions, Genetic, Tetradecanoylphorbol Acetate, Transcription, Genetic, HIV-1, Transcriptional Activation, Gene Products, tat, Genome, Human, Gene Expression Regulation, Viral, HIV Long Terminal Repeat, Virus Integration, Cyclin-Dependent Kinases, Jurkat Cells, DNA Methylation, Cyclin-Dependent Kinase 9, tat Gene Products, Human Immunodeficiency Virus, Histone Deacetylase Inhibitors
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