期刊
OPEN BIOLOGY
卷 7, 期 10, 页码 -出版社
ROYAL SOC
DOI: 10.1098/rsob.170115
关键词
HIV-1; PHF13; integration; Vpr; virus restriction factor
资金
- Else Kroner-Fresenius Stiftung [2012_A264]
- Deutsche Forschungsgemeinschaft part of the DFG priority programme SPP1923 'Innate Sensing and Restriction of Retroviruses' [SCHI 1073/7-1]
Viruses interact with multiple host cell factors. Some of these are required to promote viral propagation, others have roles in inhibiting infection. Here, we delineate the function of the cellular factor PHF13 (or SPOC1), a putative HIV-1 restriction factor. Early in the HIV-1 replication cycle PHF13 increased the number of integrated proviral copies and the number of infected cells. However, after HIV-1 integration, high levels of PHF13 suppressed viral gene expression. The antiviral activity of PHF13 is counteracted by the viral accessory protein Vpr, which mediates PHF13 degradation. Altogether, the transcriptional master regulator and chromatin binding protein PHF13 does not have purely repressive effects on HIV-1 replication, but also promotes viral integration. By the functional characterization of the dual role of PHF13 during the HIV-1 replication cycle, we reveal a surprising and intricate mechanism through which HIV-1 might regulate the switch from integration to viral gene expression. Furthermore, we identify PHF13 as a cellular target specifically degraded by HIV-1 Vpr.
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