Dynamics and regulation of nuclear import and nuclear movements of HIV-1 complexes

• Published in: PLoS pathogens Vol. 13; no. 8; p. e1006570
• Main Authors: Burdick, Ryan C, Delviks-Frankenberry, Krista A, Chen, Jianbo, Janaka, Sanath K, Sastri, Jaya, Hu, Wei-Shau, Pathak, Vinay K
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 21-08-2017; Public Library of Science (PLoS)
• Subjects: Active Transport, Cell Nucleus - physiology; Analysis; Biology and Life Sciences; Blotting, Western; Cancer; Cell Line; Cell Nucleus - metabolism; Chromatin; Comparative analysis; Core loss; CRISPR; Cytoplasm; Docking; Dynamics; Fluorescent Antibody Technique; Gene expression; Gene Knockdown Techniques; Gene therapy; Health aspects; HIV; HIV Infections - metabolism; HIV-1 - metabolism; Human immunodeficiency virus; Humans; Imports; Infections; Integrase; Kinetics; Medical research; Medicine and Health Sciences; Microscopy, Confocal; Mutation; Nuclear Envelope - metabolism; Nuclear membrane; Nuclear Pore Complex Proteins - metabolism; Nuclear transport; Nuclei (cytology); Proteins; Research and analysis methods; Reverse transcription; Tethering; Transcription (Genetics); Translocation; Uncoating; Virions; Virus Integration - physiology; Virus Uncoating - physiology
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1006570

The dynamics and regulation of HIV-1 nuclear import and its intranuclear movements after import have not been studied. To elucidate these essential HIV-1 post-entry events, we labeled viral complexes with two fluorescently tagged virion-incorporated proteins (APOBEC3F or integrase), and analyzed the HIV-1 dynamics of nuclear envelope (NE) docking, nuclear import, and intranuclear movements in living cells. We observed that HIV-1 complexes exhibit unusually long NE residence times (1.5±1.6 hrs) compared to most cellular cargos, which are imported into the nuclei within milliseconds. Furthermore, nuclear import requires HIV-1 capsid (CA) and nuclear pore protein Nup358, and results in significant loss of CA, indicating that one of the viral core uncoating steps occurs during nuclear import. Our results showed that the CA-Cyclophilin A interaction regulates the dynamics of nuclear import by delaying the time of NE docking as well as transport through the nuclear pore, but blocking reverse transcription has no effect on the kinetics of nuclear import. We also visualized the translocation of viral complexes docked at the NE into the nucleus and analyzed their nuclear movements and determined that viral complexes exhibited a brief fast phase (<9 min), followed by a long slow phase lasting several hours. A comparison of the movement of viral complexes to those of proviral transcription sites supports the hypothesis that HIV-1 complexes quickly tether to chromatin at or near their sites of integration in both wild-type cells and cells in which LEDGF/p75 was deleted using CRISPR/cas9, indicating that the tethering interactions do not require LEDGF/p75. These studies provide novel insights into the dynamics of viral complex-NE association, regulation of nuclear import, viral core uncoating, and intranuclear movements that precede integration site selection.