IQGAP1 Negatively Regulates HIV-1 Gag Trafficking and Virion Production
Summary: IQGAP1 is a master regulator of many cellular processes, including intracellular vesicle trafficking and endocytosis. We show that depletion of IQGAP1 in a variety of cell types increases the release of HIV-1 infectious virions and that overexpression diminishes virion production, with neit...
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doaj-efc7777fa6ff46f1a0a292a444fb3fc82020-11-25T03:12:27ZengElsevierCell Reports2211-12472020-03-01301240654081.e4IQGAP1 Negatively Regulates HIV-1 Gag Trafficking and Virion ProductionYosef Sabo0Kenia de los Santos1Stephen P. Goff2Howard Hughes Medical Institute, Columbia University, New York, NY 10032, USA; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA; Department of Microbiology and Immunology, Columbia University, New York, NY 10032, USA; Department of Medicine, Division of Infectious Diseases, Columbia University, New York, NY 10032, USAHoward Hughes Medical Institute, Columbia University, New York, NY 10032, USA; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA; Department of Microbiology and Immunology, Columbia University, New York, NY 10032, USAHoward Hughes Medical Institute, Columbia University, New York, NY 10032, USA; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA; Department of Microbiology and Immunology, Columbia University, New York, NY 10032, USA; Corresponding authorSummary: IQGAP1 is a master regulator of many cellular processes, including intracellular vesicle trafficking and endocytosis. We show that depletion of IQGAP1 in a variety of cell types increases the release of HIV-1 infectious virions and that overexpression diminishes virion production, with neither affecting the early stages of infection. IQGAP1 negatively regulates the steady-state levels of HIV-1 Gag at the plasma membrane, the site of assembly. We establish that IQGAP1 interacts with both the nucleocapsid and p6 domains of Gag, and interaction with either domain is sufficient for its regulatory function. Finally, we demonstrate that IQGAP1 regulation is independent of HIV-1 Gag “late-domains” sequences required by the virus to recruit the cellular ESCRT machinery. Thus, we provide evidence that IQGAP1 is a negative regulatory factor inhibiting efficient budding of HIV-1 by reducing Gag accumulation at the plasma membrane. : IQGAP1 is a ubiquitously expressed master regulator of many cellular processes, including intracellular trafficking. Sabo et al. demonstrate that in a variety of cell types, IQGAP1 acts as a negative regulator of HIV-1 viral particle release by reducing accumulation of the Gag viral structural protein at the plasma membrane. Keywords: IQGAP1 inhibition of HIV-1, IQGAP1-Gag interaction, HIV-1 virion formation, HIV-1 Gag traffickinghttp://www.sciencedirect.com/science/article/pii/S2211124720303004 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yosef Sabo Kenia de los Santos Stephen P. Goff |
spellingShingle |
Yosef Sabo Kenia de los Santos Stephen P. Goff IQGAP1 Negatively Regulates HIV-1 Gag Trafficking and Virion Production Cell Reports |
author_facet |
Yosef Sabo Kenia de los Santos Stephen P. Goff |
author_sort |
Yosef Sabo |
title |
IQGAP1 Negatively Regulates HIV-1 Gag Trafficking and Virion Production |
title_short |
IQGAP1 Negatively Regulates HIV-1 Gag Trafficking and Virion Production |
title_full |
IQGAP1 Negatively Regulates HIV-1 Gag Trafficking and Virion Production |
title_fullStr |
IQGAP1 Negatively Regulates HIV-1 Gag Trafficking and Virion Production |
title_full_unstemmed |
IQGAP1 Negatively Regulates HIV-1 Gag Trafficking and Virion Production |
title_sort |
iqgap1 negatively regulates hiv-1 gag trafficking and virion production |
publisher |
Elsevier |
series |
Cell Reports |
issn |
2211-1247 |
publishDate |
2020-03-01 |
description |
Summary: IQGAP1 is a master regulator of many cellular processes, including intracellular vesicle trafficking and endocytosis. We show that depletion of IQGAP1 in a variety of cell types increases the release of HIV-1 infectious virions and that overexpression diminishes virion production, with neither affecting the early stages of infection. IQGAP1 negatively regulates the steady-state levels of HIV-1 Gag at the plasma membrane, the site of assembly. We establish that IQGAP1 interacts with both the nucleocapsid and p6 domains of Gag, and interaction with either domain is sufficient for its regulatory function. Finally, we demonstrate that IQGAP1 regulation is independent of HIV-1 Gag “late-domains” sequences required by the virus to recruit the cellular ESCRT machinery. Thus, we provide evidence that IQGAP1 is a negative regulatory factor inhibiting efficient budding of HIV-1 by reducing Gag accumulation at the plasma membrane. : IQGAP1 is a ubiquitously expressed master regulator of many cellular processes, including intracellular trafficking. Sabo et al. demonstrate that in a variety of cell types, IQGAP1 acts as a negative regulator of HIV-1 viral particle release by reducing accumulation of the Gag viral structural protein at the plasma membrane. Keywords: IQGAP1 inhibition of HIV-1, IQGAP1-Gag interaction, HIV-1 virion formation, HIV-1 Gag trafficking |
url |
http://www.sciencedirect.com/science/article/pii/S2211124720303004 |
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