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Nuclear Envelope Protein SUN2 Promotes Cyclophilin-A-Dependent Steps of HIV Replication
Author(s) -
Xavier Lahaye,
Takeshi Satoh,
Matteo Gentili,
Silvia Cerboni,
Aymeric Silvin,
Cécile Conrad,
Abdelhakim Ahmed–Belkacem,
Elisa C. Rodriguez,
JeanFrançois Guichou,
Nathalie Bosquet,
Matthieu Piel,
Roger Le Grand,
Megan C. King,
JeanMichel Pawlotsky,
Nicolas Manel
Publication year - 2016
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2016.03.074
Subject(s) - cypa , cyclophilin a , biology , capsid , viral replication , microbiology and biotechnology , host factor , virology , nuclear transport , samhd1 , reverse transcriptase , genetics , virus , rna , cell nucleus , gene , nucleus
During the early phase of replication, HIV reverse transcribes its RNA and crosses the nuclear envelope while escaping host antiviral defenses. The host factor Cyclophilin A (CypA) is essential for these steps and binds the HIV capsid; however, the mechanism underlying this effect remains elusive. Here, we identify related capsid mutants in HIV-1, HIV-2, and SIVmac that are restricted by CypA. This antiviral restriction of mutated viruses is conserved across species and prevents nuclear import of the viral cDNA. Importantly, the inner nuclear envelope protein SUN2 is required for the antiviral activity of CypA. We show that wild-type HIV exploits SUN2 in primary CD4 + T cells as an essential host factor that is required for the positive effects of CypA on reverse transcription and infection. Altogether, these results establish essential CypA-dependent functions of SUN2 in HIV infection at the nuclear envelope.

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