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Characterization of Endogenous SERINC5 Protein as Anti-HIV-1 Factor

Authors :
Passos, Vania
Zillinger, Thomas
Casartelli, Nicoletta
Wachs, Amelie S.
Xu, Shuting
Malassa, Angelina
Steppich, Katja
Schilling, Hildegard
Franz, Sergej
Todt, Daniel
Steinmann, Eike
Sutter, Kathrin
Dittmer, Ulf
Bohne, Jens
Schwartz, Olivier
Barchet, Winfried
Goffinet, Christine
Passos, Vania
Zillinger, Thomas
Casartelli, Nicoletta
Wachs, Amelie S.
Xu, Shuting
Malassa, Angelina
Steppich, Katja
Schilling, Hildegard
Franz, Sergej
Todt, Daniel
Steinmann, Eike
Sutter, Kathrin
Dittmer, Ulf
Bohne, Jens
Schwartz, Olivier
Barchet, Winfried
Goffinet, Christine
Publication Year :
2019

Abstract

When expressed in virus-producing cells, the cellular multipass transmembrane protein SERINC5 reduces the infectivity of HIV-1 particles and is counteracted by HIV-1 Nef. Due to the unavailability of an antibody of sufficient specificity and sensitivity, investigation of SERINC5 protein expression and subcellular localization has been limited to heterologously expressed SERINC5. We generated, via CRISPR/Cas9-assisted gene editing, Jurkat T-cell clones expressing endogenous SERINC5 bearing an extracellularly exposed hemagglutinin (HA) epitope [Jurkat SERINC5(iHA knock-in) T cells]. This modification enabled quantification of endogenous SERINC5 protein levels and demonstrated a predominant localization in lipid rafts. Interferon alpha (IFN-alpha) treatment enhanced cell surface levels of SERINC5 in a ruxolitinib-sensitive manner in the absence of modulation of mRNA and protein quantities. Parental and SERINC5(iHA knock-in) T cells shared the ability to produce infectious wild-type HIV-1 but not an HIV-1 Delta nef mutant. SERINC5-imposed reduction of infectivity involved a modest reduction of virus fusogenicity. An association of endogenous SERINC5 protein with HIV-1 Delta nef virions was consistently detectable as a 35-kDa species, as opposed to heterologous SERINC5, which presented as a 51-kDa species. Nef-mediated functional counteraction did not correlate with virion exclusion of SERINC5, arguing for the existence of additional counteractive mechanisms of Nef that act on virusassociated SERINC5. In HIV-1-infected cells, Nef triggered the internalization of SERINC5 in the absence of detectable changes of steady-state protein levels. These findings establish new properties of endogenous SERINC5 expression and subcellular localization, challenge existing concepts of HIV-1 Nef-mediated antagonism of SERINC5, and uncover an unprecedented role of IFN-alpha in modulating SERINC5 through accumulation at the cell surface. IMPORTANCE SERINC5 is the long-searched-for antivira

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1364904665
Document Type :
Electronic Resource