Balance between retroviral latency and transcription : based on HIV model
- Autores
- Pluta, Aneta; Jaworski, Juan Pablo; Cortés-Rubio, César N.
- Año de publicación
- 2021
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The representative of the Lentivirus genus is the human immunodeficiency virus type 1 (HIV-1), the causative agent of acquired immunodeficiency syndrome (AIDS). To date, there is no cure for AIDS because of the existence of the HIV-1 reservoir. HIV-1 infection can persist for decades despite effective antiretroviral therapy (ART), due to the persistence of infectious latent viruses in long-lived resting memory CD4+ T cells, macrophages, monocytes, microglial cells, and other cell types. However, the biology of HIV-1 latency remains incompletely understood. Retroviral long terminal repeat region (LTR) plays an indispensable role in controlling viral gene expression. Regulation of the transcription initiation plays a crucial role in establishing and maintaining a retrovirus latency. Whether and how retroviruses establish latency and reactivate remains unclear. In this article, we describe what is known about the regulation of LTR-driven transcription in HIV-1, that is, the cis-elements present in the LTR, the role of LTR transcription factor binding sites in LTR-driven transcription, the role of HIV-1-encoded transactivator protein, hormonal effects on virus transcription, impact of LTR variability on transcription, and epigenetic control of retrovirus LTR. Finally, we focus on a novel clustered regularly interspaced short palindromic repeats-associated protein 9 (CRISPR/dCas9)-based strategy for HIV-1 reservoir purging.
Instituto de Virología
Fil: Pluta, Aneta. National Veterinary Research Institute. Department of Biochemistry; Polonia
Fil: Jaworski, Juan Pablo. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; Argentina
Fil: Jaworski, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Tecnológicas; Argentina
Fil: Cortés-Rubio, César N. National Institute of Respiratory Diseases. Centre for Research in Infectious Diseases; México - Fuente
- Pathogens 10 (1) : 16 (Enero 2021)
- Materia
-
Retroviridae
Virus de la Inmunodeficiencia Humana
Infección por VIH
Infecciones Latentes
Repeticiones Palindrómicas Cortas Agrupadas y Regularmente Interespaciadas
Transcripción
Lentivirus
Human Immunodeficiency Virus
HIV Infections
Latent Infections
CRISPR
Transcription - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
- Institución
- Instituto Nacional de Tecnología Agropecuaria
- OAI Identificador
- oai:localhost:20.500.12123/9143
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Balance between retroviral latency and transcription : based on HIV modelPluta, AnetaJaworski, Juan PabloCortés-Rubio, César N.RetroviridaeVirus de la Inmunodeficiencia HumanaInfección por VIHInfecciones LatentesRepeticiones Palindrómicas Cortas Agrupadas y Regularmente InterespaciadasTranscripciónLentivirusHuman Immunodeficiency VirusHIV InfectionsLatent InfectionsCRISPRTranscriptionThe representative of the Lentivirus genus is the human immunodeficiency virus type 1 (HIV-1), the causative agent of acquired immunodeficiency syndrome (AIDS). To date, there is no cure for AIDS because of the existence of the HIV-1 reservoir. HIV-1 infection can persist for decades despite effective antiretroviral therapy (ART), due to the persistence of infectious latent viruses in long-lived resting memory CD4+ T cells, macrophages, monocytes, microglial cells, and other cell types. However, the biology of HIV-1 latency remains incompletely understood. Retroviral long terminal repeat region (LTR) plays an indispensable role in controlling viral gene expression. Regulation of the transcription initiation plays a crucial role in establishing and maintaining a retrovirus latency. Whether and how retroviruses establish latency and reactivate remains unclear. In this article, we describe what is known about the regulation of LTR-driven transcription in HIV-1, that is, the cis-elements present in the LTR, the role of LTR transcription factor binding sites in LTR-driven transcription, the role of HIV-1-encoded transactivator protein, hormonal effects on virus transcription, impact of LTR variability on transcription, and epigenetic control of retrovirus LTR. Finally, we focus on a novel clustered regularly interspaced short palindromic repeats-associated protein 9 (CRISPR/dCas9)-based strategy for HIV-1 reservoir purging.Instituto de VirologíaFil: Pluta, Aneta. National Veterinary Research Institute. Department of Biochemistry; PoloniaFil: Jaworski, Juan Pablo. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; ArgentinaFil: Jaworski, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Tecnológicas; ArgentinaFil: Cortés-Rubio, César N. National Institute of Respiratory Diseases. Centre for Research in Infectious Diseases; MéxicoMDPI2021-04-21T14:25:05Z2021-04-21T14:25:05Z2021-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12123/9143https://www.mdpi.com/2076-0817/10/1/162076-0817https://doi.org/10.3390/pathogens10010016Pathogens 10 (1) : 16 (Enero 2021)reponame:INTA Digital (INTA)instname:Instituto Nacional de Tecnología Agropecuariaenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)2025-09-29T13:45:11Zoai:localhost:20.500.12123/9143instacron:INTAInstitucionalhttp://repositorio.inta.gob.ar/Organismo científico-tecnológicoNo correspondehttp://repositorio.inta.gob.ar/oai/requesttripaldi.nicolas@inta.gob.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:l2025-09-29 13:45:11.868INTA Digital (INTA) - Instituto Nacional de Tecnología Agropecuariafalse |
dc.title.none.fl_str_mv |
Balance between retroviral latency and transcription : based on HIV model |
title |
Balance between retroviral latency and transcription : based on HIV model |
spellingShingle |
Balance between retroviral latency and transcription : based on HIV model Pluta, Aneta Retroviridae Virus de la Inmunodeficiencia Humana Infección por VIH Infecciones Latentes Repeticiones Palindrómicas Cortas Agrupadas y Regularmente Interespaciadas Transcripción Lentivirus Human Immunodeficiency Virus HIV Infections Latent Infections CRISPR Transcription |
title_short |
Balance between retroviral latency and transcription : based on HIV model |
title_full |
Balance between retroviral latency and transcription : based on HIV model |
title_fullStr |
Balance between retroviral latency and transcription : based on HIV model |
title_full_unstemmed |
Balance between retroviral latency and transcription : based on HIV model |
title_sort |
Balance between retroviral latency and transcription : based on HIV model |
dc.creator.none.fl_str_mv |
Pluta, Aneta Jaworski, Juan Pablo Cortés-Rubio, César N. |
author |
Pluta, Aneta |
author_facet |
Pluta, Aneta Jaworski, Juan Pablo Cortés-Rubio, César N. |
author_role |
author |
author2 |
Jaworski, Juan Pablo Cortés-Rubio, César N. |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Retroviridae Virus de la Inmunodeficiencia Humana Infección por VIH Infecciones Latentes Repeticiones Palindrómicas Cortas Agrupadas y Regularmente Interespaciadas Transcripción Lentivirus Human Immunodeficiency Virus HIV Infections Latent Infections CRISPR Transcription |
topic |
Retroviridae Virus de la Inmunodeficiencia Humana Infección por VIH Infecciones Latentes Repeticiones Palindrómicas Cortas Agrupadas y Regularmente Interespaciadas Transcripción Lentivirus Human Immunodeficiency Virus HIV Infections Latent Infections CRISPR Transcription |
dc.description.none.fl_txt_mv |
The representative of the Lentivirus genus is the human immunodeficiency virus type 1 (HIV-1), the causative agent of acquired immunodeficiency syndrome (AIDS). To date, there is no cure for AIDS because of the existence of the HIV-1 reservoir. HIV-1 infection can persist for decades despite effective antiretroviral therapy (ART), due to the persistence of infectious latent viruses in long-lived resting memory CD4+ T cells, macrophages, monocytes, microglial cells, and other cell types. However, the biology of HIV-1 latency remains incompletely understood. Retroviral long terminal repeat region (LTR) plays an indispensable role in controlling viral gene expression. Regulation of the transcription initiation plays a crucial role in establishing and maintaining a retrovirus latency. Whether and how retroviruses establish latency and reactivate remains unclear. In this article, we describe what is known about the regulation of LTR-driven transcription in HIV-1, that is, the cis-elements present in the LTR, the role of LTR transcription factor binding sites in LTR-driven transcription, the role of HIV-1-encoded transactivator protein, hormonal effects on virus transcription, impact of LTR variability on transcription, and epigenetic control of retrovirus LTR. Finally, we focus on a novel clustered regularly interspaced short palindromic repeats-associated protein 9 (CRISPR/dCas9)-based strategy for HIV-1 reservoir purging. Instituto de Virología Fil: Pluta, Aneta. National Veterinary Research Institute. Department of Biochemistry; Polonia Fil: Jaworski, Juan Pablo. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; Argentina Fil: Jaworski, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Tecnológicas; Argentina Fil: Cortés-Rubio, César N. National Institute of Respiratory Diseases. Centre for Research in Infectious Diseases; México |
description |
The representative of the Lentivirus genus is the human immunodeficiency virus type 1 (HIV-1), the causative agent of acquired immunodeficiency syndrome (AIDS). To date, there is no cure for AIDS because of the existence of the HIV-1 reservoir. HIV-1 infection can persist for decades despite effective antiretroviral therapy (ART), due to the persistence of infectious latent viruses in long-lived resting memory CD4+ T cells, macrophages, monocytes, microglial cells, and other cell types. However, the biology of HIV-1 latency remains incompletely understood. Retroviral long terminal repeat region (LTR) plays an indispensable role in controlling viral gene expression. Regulation of the transcription initiation plays a crucial role in establishing and maintaining a retrovirus latency. Whether and how retroviruses establish latency and reactivate remains unclear. In this article, we describe what is known about the regulation of LTR-driven transcription in HIV-1, that is, the cis-elements present in the LTR, the role of LTR transcription factor binding sites in LTR-driven transcription, the role of HIV-1-encoded transactivator protein, hormonal effects on virus transcription, impact of LTR variability on transcription, and epigenetic control of retrovirus LTR. Finally, we focus on a novel clustered regularly interspaced short palindromic repeats-associated protein 9 (CRISPR/dCas9)-based strategy for HIV-1 reservoir purging. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-04-21T14:25:05Z 2021-04-21T14:25:05Z 2021-01 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/20.500.12123/9143 https://www.mdpi.com/2076-0817/10/1/16 2076-0817 https://doi.org/10.3390/pathogens10010016 |
url |
http://hdl.handle.net/20.500.12123/9143 https://www.mdpi.com/2076-0817/10/1/16 https://doi.org/10.3390/pathogens10010016 |
identifier_str_mv |
2076-0817 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
MDPI |
publisher.none.fl_str_mv |
MDPI |
dc.source.none.fl_str_mv |
Pathogens 10 (1) : 16 (Enero 2021) reponame:INTA Digital (INTA) instname:Instituto Nacional de Tecnología Agropecuaria |
reponame_str |
INTA Digital (INTA) |
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INTA Digital (INTA) |
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Instituto Nacional de Tecnología Agropecuaria |
repository.name.fl_str_mv |
INTA Digital (INTA) - Instituto Nacional de Tecnología Agropecuaria |
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tripaldi.nicolas@inta.gob.ar |
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