Reconstitution and visualization of HIV-1 capsid-dependent replication and integration in vitro.
Devin E ChristensenBarbie K Ganser-PornillosJarrod S JohnsonOwen PornillosWesley I SundquistPublished in: Science (New York, N.Y.) (2020)
During the first half of the viral life cycle, HIV-1 reverse transcribes its RNA genome and integrates the double-stranded DNA copy into a host cell chromosome. Despite progress in characterizing and inhibiting these processes, in situ mechanistic and structural studies remain challenging. This is because these operations are executed by individual viral preintegration complexes deep within cells. We therefore reconstituted and imaged the early stages of HIV-1 replication in a cell-free system. HIV-1 cores released from permeabilized virions supported efficient, capsid-dependent endogenous reverse transcription to produce double-stranded DNA genomes, which sometimes looped out from ruptured capsid walls. Concerted integration of both viral DNA ends into a target plasmid then proceeded in a cell extract-dependent reaction. This reconstituted system uncovers the role of the capsid in templating replication.
Keyphrases
- cell free
- antiretroviral therapy
- hiv positive
- hiv infected
- hiv testing
- circulating tumor
- human immunodeficiency virus
- hepatitis c virus
- hiv aids
- men who have sex with men
- sars cov
- nucleic acid
- single molecule
- single cell
- induced apoptosis
- life cycle
- oxidative stress
- escherichia coli
- high density
- signaling pathway
- south africa
- cell proliferation
- endoplasmic reticulum stress
- gene expression
- transcription factor
- cell death
- pi k akt