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Regulation of CDK9 Activity by Phosphorylation and Dephosphorylation

HIV-1 transcription is regulated by CDK9/cyclin T1, which, unlike a typical cell cycle-dependent kinase, is regulated by associating with 7SK small nuclear ribonuclear protein complex (snRNP). While the protein components of this complex are well studied, the mechanism of the complex formation is st...

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Detalles Bibliográficos
Autores principales: Nekhai, Sergei, Petukhov, Michael, Breuer, Denitra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913462/
https://www.ncbi.nlm.nih.gov/pubmed/24524087
http://dx.doi.org/10.1155/2014/964964
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author Nekhai, Sergei
Petukhov, Michael
Breuer, Denitra
author_facet Nekhai, Sergei
Petukhov, Michael
Breuer, Denitra
author_sort Nekhai, Sergei
collection PubMed
description HIV-1 transcription is regulated by CDK9/cyclin T1, which, unlike a typical cell cycle-dependent kinase, is regulated by associating with 7SK small nuclear ribonuclear protein complex (snRNP). While the protein components of this complex are well studied, the mechanism of the complex formation is still not fully understood. The association of CDK9/cyclin T1 with 7SK snRNP is, in part, regulated by a reversible CDK9 phosphorylation. Here, we present a comprehensive review of the kinases and phosphatases involved in CDK9 phosphorylation and discuss their role in regulation of HIV-1 replication and potential for being targeted for drug development. We propose a novel pathway of HIV-1 transcription regulation via CDK9 Ser-90 phosphorylation by CDK2 and CDK9 Ser-175 dephosphorylation by protein phosphatase-1.
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spelling pubmed-39134622014-02-12 Regulation of CDK9 Activity by Phosphorylation and Dephosphorylation Nekhai, Sergei Petukhov, Michael Breuer, Denitra Biomed Res Int Review Article HIV-1 transcription is regulated by CDK9/cyclin T1, which, unlike a typical cell cycle-dependent kinase, is regulated by associating with 7SK small nuclear ribonuclear protein complex (snRNP). While the protein components of this complex are well studied, the mechanism of the complex formation is still not fully understood. The association of CDK9/cyclin T1 with 7SK snRNP is, in part, regulated by a reversible CDK9 phosphorylation. Here, we present a comprehensive review of the kinases and phosphatases involved in CDK9 phosphorylation and discuss their role in regulation of HIV-1 replication and potential for being targeted for drug development. We propose a novel pathway of HIV-1 transcription regulation via CDK9 Ser-90 phosphorylation by CDK2 and CDK9 Ser-175 dephosphorylation by protein phosphatase-1. Hindawi Publishing Corporation 2014 2014-01-12 /pmc/articles/PMC3913462/ /pubmed/24524087 http://dx.doi.org/10.1155/2014/964964 Text en Copyright © 2014 Sergei Nekhai et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Nekhai, Sergei
Petukhov, Michael
Breuer, Denitra
Regulation of CDK9 Activity by Phosphorylation and Dephosphorylation
title Regulation of CDK9 Activity by Phosphorylation and Dephosphorylation
title_full Regulation of CDK9 Activity by Phosphorylation and Dephosphorylation
title_fullStr Regulation of CDK9 Activity by Phosphorylation and Dephosphorylation
title_full_unstemmed Regulation of CDK9 Activity by Phosphorylation and Dephosphorylation
title_short Regulation of CDK9 Activity by Phosphorylation and Dephosphorylation
title_sort regulation of cdk9 activity by phosphorylation and dephosphorylation
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913462/
https://www.ncbi.nlm.nih.gov/pubmed/24524087
http://dx.doi.org/10.1155/2014/964964
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