Unknown

Dataset Information

0

Filamin A protein interacts with human immunodeficiency virus type 1 Gag protein and contributes to productive particle assembly.


ABSTRACT: HIV-1 Gag precursor directs virus particle assembly and release. In a search for Gag-interacting proteins that are involved in late stages of the HIV-1 replication cycle, we performed yeast two-hybrid screening against a human cDNA library and identified the non-muscle actin filament cross-linking protein filamin A as a novel Gag binding partner. The 280-kDa filamin A regulates cortical actin network dynamics and participates in the anchoring of membrane proteins to the actin cytoskeleton. Recent studies have shown that filamin A facilitates HIV-1 cell-to-cell transmission by binding to HIV receptors and coreceptors and regulating their clustering on the target cell surface. Here we report a novel role for filamin A in HIV-1 Gag intracellular trafficking. We demonstrate that filamin A interacts with the capsid domain of HIV-1 Gag and that this interaction is involved in particle release in a productive manner. Disruption of this interaction eliminated Gag localization at the plasma membrane and induced Gag accumulation within internal compartments. Moreover, blocking clathrin-dependent endocytic pathways did not relieve the restriction to particle release induced by filamin A depletion. These results suggest that filamin A is involved in the distinct step of the Gag trafficking pathway. The discovery of the Gag-filamin A interaction may provide a new therapeutic target for the treatment of HIV infection.

SUBMITTER: Cooper J 

PROVIDER: S-EPMC3151092 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC7290722 | biostudies-literature
| S-EPMC6783973 | biostudies-literature
| S-EPMC1211529 | biostudies-literature
| S-EPMC229285 | biostudies-literature
| S-EPMC4051761 | biostudies-literature
| S-EPMC1563813 | biostudies-literature
| S-EPMC4791233 | biostudies-literature
| S-EPMC5977254 | biostudies-literature
| S-EPMC6026748 | biostudies-literature
| S-EPMC2681934 | biostudies-literature