Ireplicon assay revealed that the X proteins of ABVs, but not RBV, can inhibit the polymerase activity of BDV. Our results suggest that although RBV may have evolved the X 57773-65-6 web protein in a genotype- and/or host-specific manner, the fundamental function of the X protein as a regulator of the intranuclear level of P has been preserved among bornaviruses throughout their evolution.Plasmid ConstructionTo generate the eukaryotic expression plasmids, PCR amplified (-)-Indolactam V bornavirus X and P genes were cloned into the plasmid pcDNA3 (Invitrogen). The BDV X and P genes were amplified from cDNA from BDV-infected OL cells. The X gene primer included a Flag tag sequence and the P gene vector contained a HA tag sequence. Then, each X protein was expressed as a Flag fusion protein and each P protein was expressed as an HA fusion protein. Nucleotide sequences of the recombinant constructs were confirmed by DNA sequencing.Immunoprecipitation AssaysThe 293T cells were seeded in 10 cm plates. One day after seeding, cells were transfected with Flag-tagged bornavirus X and/ or HA-tagged bornavirus P plasmids using Lipofectamine 2000. At 24 h posttransfection, the media were removed from the plates by aspiration and the 293T cells were washed with PBS. Cells were then scraped with 1 ml PBS. After centrifugation (2,500 rpm, 1 min), the PBS was aspirated and the cells were lysed using lysis buffer (20 mM Tris-HCl pH 7.4, 150 mM NaCl, 1 TritonX100, 1 mM EDTA, protease inhibitor). To homogenize, the cell lysates were sonicated and rotated for 30 min. After centrifugation (15,000 rpm, 20 min), the supernatants were incubated with 40 ml of pre-equilibrated anti-HA resin (Sigma-Aldrich) overnight with rotation. After incubation, beads were collected by centrifugation at 12,000 rpm for 1 min and washed three times with 1 ml of lysis buffer. The proteins immunoprecipitated with anti-HA resin were detected by western blotting. All methods used during the harvesting procedure were performed at 4uC. Western blot analysis was performed using standard techniques and 15 SDS polyacrylamide gel electrophoresis (PAGE). The rabbit anti-Flag antibody (Sigma-Aldrich) was diluted 1:1,000, the rabbit anti-HA antibody (Santa Cruz) was diluted 1:1,000 in 5 low-fat milk powder in PBS or Can Get Signal (TOYOBO) and incubated 1317923 with membranes overnight at 4uC. After washing the samples three times for 10 min with PBS-0.1 Tween-20, antibodies were detected using horseradish peroxidase-coupled goat anti-rabbit or anti-mouse antibodies (Jackson ImmunoResearch) diluted 1:5,000 in 5 low-fat milk powder in PBS or Can Get Signal, and visualization was performed using ECL Plus Western Blot Detection Reagents (GE Healthcare) according to the manufacturer’s instructions.Materials and Methods CellsThe OL cell line [19], derived from a human oligodendroglioma, and BDV-infected OL cells were cultured in Dulbecco’s modified Eagle’s medium containing 5 fetal bovine serum. Human HEK-293T cells and QT6 cells (American Type Culture Collection, CRL-1708), derived from quail were maintained in Dulbecco’s modified Eagle’s medium containing 10 fatal bovine serum. Cells were cultured at 37uC under 5 CO2.Figure 1. Schematic representation of BDV genome. An illustration of the genome organization of BDV is shown at the top. The genome region corresponding to the 59 UTR of X/P mRNA is enlarged in the center. The arrow indicates a schematic structure of X/P mRNA. The open circle on X/P mRNA indicates the region of a.Ireplicon assay revealed that the X proteins of ABVs, but not RBV, can inhibit the polymerase activity of BDV. Our results suggest that although RBV may have evolved the X protein in a genotype- and/or host-specific manner, the fundamental function of the X protein as a regulator of the intranuclear level of P has been preserved among bornaviruses throughout their evolution.Plasmid ConstructionTo generate the eukaryotic expression plasmids, PCR amplified bornavirus X and P genes were cloned into the plasmid pcDNA3 (Invitrogen). The BDV X and P genes were amplified from cDNA from BDV-infected OL cells. The X gene primer included a Flag tag sequence and the P gene vector contained a HA tag sequence. Then, each X protein was expressed as a Flag fusion protein and each P protein was expressed as an HA fusion protein. Nucleotide sequences of the recombinant constructs were confirmed by DNA sequencing.Immunoprecipitation AssaysThe 293T cells were seeded in 10 cm plates. One day after seeding, cells were transfected with Flag-tagged bornavirus X and/ or HA-tagged bornavirus P plasmids using Lipofectamine 2000. At 24 h posttransfection, the media were removed from the plates by aspiration and the 293T cells were washed with PBS. Cells were then scraped with 1 ml PBS. After centrifugation (2,500 rpm, 1 min), the PBS was aspirated and the cells were lysed using lysis buffer (20 mM Tris-HCl pH 7.4, 150 mM NaCl, 1 TritonX100, 1 mM EDTA, protease inhibitor). To homogenize, the cell lysates were sonicated and rotated for 30 min. After centrifugation (15,000 rpm, 20 min), the supernatants were incubated with 40 ml of pre-equilibrated anti-HA resin (Sigma-Aldrich) overnight with rotation. After incubation, beads were collected by centrifugation at 12,000 rpm for 1 min and washed three times with 1 ml of lysis buffer. The proteins immunoprecipitated with anti-HA resin were detected by western blotting. All methods used during the harvesting procedure were performed at 4uC. Western blot analysis was performed using standard techniques and 15 SDS polyacrylamide gel electrophoresis (PAGE). The rabbit anti-Flag antibody (Sigma-Aldrich) was diluted 1:1,000, the rabbit anti-HA antibody (Santa Cruz) was diluted 1:1,000 in 5 low-fat milk powder in PBS or Can Get Signal (TOYOBO) and incubated 1317923 with membranes overnight at 4uC. After washing the samples three times for 10 min with PBS-0.1 Tween-20, antibodies were detected using horseradish peroxidase-coupled goat anti-rabbit or anti-mouse antibodies (Jackson ImmunoResearch) diluted 1:5,000 in 5 low-fat milk powder in PBS or Can Get Signal, and visualization was performed using ECL Plus Western Blot Detection Reagents (GE Healthcare) according to the manufacturer’s instructions.Materials and Methods CellsThe OL cell line [19], derived from a human oligodendroglioma, and BDV-infected OL cells were cultured in Dulbecco’s modified Eagle’s medium containing 5 fetal bovine serum. Human HEK-293T cells and QT6 cells (American Type Culture Collection, CRL-1708), derived from quail were maintained in Dulbecco’s modified Eagle’s medium containing 10 fatal bovine serum. Cells were cultured at 37uC under 5 CO2.Figure 1. Schematic representation of BDV genome. An illustration of the genome organization of BDV is shown at the top. The genome region corresponding to the 59 UTR of X/P mRNA is enlarged in the center. The arrow indicates a schematic structure of X/P mRNA. The open circle on X/P mRNA indicates the region of a.
