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. 2000 Oct;74(19):9152–9166. doi: 10.1128/jvi.74.19.9152-9166.2000

FIG. 6.

FIG. 6

FIG. 6

Cell cycle analysis of HeLa T4 cells expressing P, V, or VΔC proteins. HeLa T4 cells were synchronized as described in the legend to Fig. 2. After release from the G1-S-phase block, cells were transfected with 2 μg of the following plasmids: pCAGGS, pCAGGS-P, pCAGGS-V, or pCAGGS-VΔC. The cells were treated and analyzed as described in the legend for Fig. 3. The population of cells expressing high levels of V protein were selected for analysis. (A) The panels show representative flow cytometry data at the 44-h time point. The density plots graph DNA content (FL2-A) versus the level of P or V protein expression (FL1-H). The density plots show the selection of the high-expressing population of transfected cells (gate R2). (B) The DNA content (FL2-A) histograms of the high-expressing population of cells at 44 h post-release of synchronization block are shown. (C, D, and E) The percentage of cells in G0-G1 phase (C), S phase (D), and G2-M phase (E) are shown. Each time point is the average of three plates of cells. (F, G, and H) Cell cycle analysis and cyclin expression for HeLa T4 cells expressing P, V, or VΔC. Cells were treated as described in the legend for Fig. 2. Each time point represents the average of three plates of cells. Symbols: ⧫, control vector-transfected cells; Created by potrace 1.16, written by Peter Selinger 2001-2019 , P-expressing cells; ▴, V-expressing cells; Inline graphic, VΔC-transfected cells.