HIV-1 uncoats in the nucleus near sites of integration

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 117; no. 10; pp. 5486 - 5493
• Main Authors: Burdick, Ryan C., Li, Chenglei, Munshi, MohamedHusen, Rawson, Jonathan M. O., Nagashima, Kunio, Hu, Wei-Shau, Pathak, Vinay K.
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 10-03-2020
• Series: From the Cover
• Subjects: Biological Sciences; Capsid protein; Chromosomes; Cores; Cytoplasm; Deoxyribonucleic acid; DNA; Genomics; HIV; Human immunodeficiency virus; Imports; Innate immunity; Integration; Labeling; Nuclear pores; Nuclear transport; Polyadenylation; Protein transport; Proteins; Reverse transcription; Uncoating; Virions; HIV-1; integration; uncoating; transcription; capsid
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1920631117

HIV-1 capsid core disassembly (uncoating) must occur before integration of viral genomic DNA into the host chromosomes, yet remarkably, the timing and cellular location of uncoating is unknown. Previous studies have proposed that intact viral cores are too large to fit through nuclear pores and uncoating occurs in the cytoplasm in coordination with reverse transcription or at the nuclear envelope during nuclear import. The capsid protein (CA) content of the infectious viral cores is not well defined because methods for directly labeling and quantifying the CA in viral cores have been unavailable. In addition, it has been difficult to identify the infectious virions because only one of ~50 virions in infected cells leads to productive infection. Here, we developed methods to analyze HIV-1 uncoating by direct labeling of CA with GFP and to identify infectious virions by tracking viral cores in living infected cells through viral DNA integration and proviral DNA transcription. Astonishingly, our results show that intact (or nearly intact) viral cores enter the nucleus through a mechanism involving interactions with host protein cleavage and polyadenylation specificity factor 6 (CPSF6), complete reverse transcription in the nucleus before uncoating, and uncoat <1.5 h before integration near (<1.5 μm) their genomic integration sites. These results fundamentally change our current understanding of HIV-1 postentry replication events including mechanisms of nuclear import, uncoating, reverse transcription, integration, and evasion of innate immunity.