Document Type
Journal Article
Publication Date
7-11-2016
Journal
Virology
Volume
497
Inclusive Pages
11-22
DOI
10.1016/j.virol.2016.06.023
Abstract
The post-entry events of HIV-1 infection occur within reverse transcription complexes derived from the viral cores entering the target cell. HIV-1 cores contain host proteins incorporated from virus-producing cells. In this report, we show that MCM5, a subunit of the hexameric minichromosome maintenance (MCM) DNA helicase complex, associates with Gag polyprotein and is incorporated into HIV-1 virions. The progeny virions depleted of MCM5 demonstrated reduced reverse transcription in newly infected cells, but integration and subsequent replication steps were not affected. Interestingly, increased packaging of MCM5 into the virions also led to reduced reverse transcription, but here viral replication was impaired. Our data suggest that incorporation of physiological amounts of MCM5 promotes aberrant reverse transcription, leading to partial incapacitation of cDNA, whereas increased MCM5 abundance leads to reduced reverse transcription and infection. Therefore, MCM5 has the properties of an inhibitory factor that interferes with production of an integration-competent cDNA product.
APA Citation
Santos, S., Obukhov, Y., Nekhai, S., Pushkarsky, T., Brichacek, B., Bukrinsky, M., & Iordanskiy, S. (2016). Cellular minichromosome maintenance complex component 5 (MCM5) is incorporated into HIV-1 virions and modulates viral replication in the newly infected cells.. Virology, 497 (). http://dx.doi.org/10.1016/j.virol.2016.06.023
Peer Reviewed
1
Open Access
1
Included in
Medical Immunology Commons, Medical Microbiology Commons, Virology Commons, Virus Diseases Commons
Comments
Reproduced with permission of Elsevier B.V. Virology