Does BCA3 Play a Role in the HIV-1 Replication Cycle?
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
29677171
PubMed Central
PMC5923506
DOI
10.3390/v10040212
PII: v10040212
Knihovny.cz E-zdroje
- Klíčová slova
- AKIP-1, BCA3, HIV-1, M-PMV, PKAc, virus incorporation,
- MeSH
- adaptorové proteiny signální transdukční genetika metabolismus MeSH
- HEK293 buňky MeSH
- HeLa buňky MeSH
- HIV-1 metabolismus fyziologie MeSH
- jaderné proteiny genetika metabolismus MeSH
- lidé MeSH
- proteinkinasy závislé na cyklickém AMP metabolismus MeSH
- replikace viru genetika MeSH
- sestavení viru MeSH
- vazba proteinů MeSH
- virion metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adaptorové proteiny signální transdukční MeSH
- AKIP1 protein, human MeSH Prohlížeč
- jaderné proteiny MeSH
- proteinkinasy závislé na cyklickém AMP MeSH
The cellular role of breast carcinoma-associated protein (BCA3), also known as A-kinase-interacting protein 1 (AKIP-1), is not fully understood. Recently, we reported that full-length, but not C-terminally truncated, BCA3 is incorporated into virions of Mason-Pfizer monkey virus, and that BCA3 enhances HIV-1 protease-induced apoptosis. In the present study, we report that BCA3 is associated with purified and subtilisin-treated HIV particles. Using a combination of immune-based methods and confocal microscopy, we show that the C-terminus of BCA3 is required for packaging into HIV-1 particles. However, we were unable to identify an HIV-1 binding domain for BCA3, and we did not observe any effect of incorporated BCA3 on HIV-1 infectivity. Interestingly, the BCA3 C-terminus was previously identified as a binding site for the catalytic subunit of protein kinase A (PKAc), a cellular protein that is specifically packaged into HIV-1 particles. Based on our analysis of PKAc⁻BCA3 interactions, we suggest that BCA3 incorporation into HIV-1 particles is mediated by its ability to interact with PKAc.
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