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Status: Bibliographieeintrag

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Verfasst von:Kuzmina, Alona [VerfasserIn]   i
 Sadhu, Lopamudra [VerfasserIn]   i
 Hasanuzzaman, Md [VerfasserIn]   i
 Fujinaga, Koh [VerfasserIn]   i
 Schwartz, Jacob C. [VerfasserIn]   i
 Fackler, Oliver Till [VerfasserIn]   i
 Taube, Ran [VerfasserIn]   i
Titel:Direct and indirect effects of CYTOR lncRNA regulate HIV gene expression
Verf.angabe:Alona Kuzmina, Lopamudra Sadhu, Md Hasanuzzaman, Koh Fujinaga, Jacob C. Schwartz, Oliver T. Fackler, Ran Taube
E-Jahr:2024
Jahr:April 25, 2024
Umfang:22 S.
Illustrationen:Illustrationen
Fussnoten:Gesehen am 25.10.2024
Titel Quelle:Enthalten in: Public Library of SciencePLoS pathogens
Ort Quelle:Lawrence, Kan. : PLoS, 2005
Jahr Quelle:2024
Band/Heft Quelle:20(2024), 4, Artikel-ID e1012172, Seite 1-22
ISSN Quelle:1553-7374
Abstract:The implementation of antiretroviral therapy (ART) has effectively restricted the transmission of Human Immunodeficiency Virus (HIV) and improved overall clinical outcomes. However, a complete cure for HIV remains out of reach, as the virus persists in a stable pool of infected cell reservoir that is resistant to therapy and thus a main barrier towards complete elimination of viral infection. While the mechanisms by which host proteins govern viral gene expression and latency are well-studied, the emerging regulatory functions of non-coding RNAs (ncRNA) in the context of T cell activation, HIV gene expression and viral latency have not yet been thoroughly explored. Here, we report the identification of the Cytoskeleton Regulator (CYTOR) long non-coding RNA (lncRNA) as an activator of HIV gene expression that is upregulated following T cell stimulation. Functional studies show that CYTOR suppresses viral latency by directly binding to the HIV promoter and associating with the cellular positive transcription elongation factor (P-TEFb) to activate viral gene expression. CYTOR also plays a global role in regulating cellular gene expression, including those involved in controlling actin dynamics. Depletion of CYTOR expression reduces cytoplasmic actin polymerization in response to T cell activation. In addition, treating HIV-infected cells with pharmacological inhibitors of actin polymerization reduces HIV gene expression. We conclude that both direct and indirect effects of CYTOR regulate HIV gene expression.
DOI:doi:10.1371/journal.ppat.1012172
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.1371/journal.ppat.1012172
 kostenfrei: Volltext: https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1012172
 DOI: https://doi.org/10.1371/journal.ppat.1012172
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Actin polymerization
 Actins
 Gene expression
 Gene regulation
 HIV
 Long non-coding RNA
 Non-coding RNA
 T helper cells
K10plus-PPN:1906822891
Verknüpfungen:→ Zeitschrift

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