Figure 1.
Figure 1. Increased posttranslational modification of p27kip1 correlates with cell-cycle entry. FACS analysis shows the percentage of cells arrested in G1/G0 (A, left panel) in primary B cells with or without treatment with PMA for 72 hours (labeled as primary B or primary B + PMA, respectively), Burkitt lymphoma cell line BL40 (labeled as BL40), (C) in H1299 cells with or without the inducible expression of p27kip1 (labeled as H1299, H1299 + p27kip1) and in Cal51 cells. Right-hand panels of A and C are Western blots showing the expression levels of p27kip1 in the corresponding cell populations used to carry out the FACS and 2D gel analysis. The isoforms 1 to 7 are indicated with arrows in panels B and D and their isoelectric points are 6.76, 6.59, 6.37, 6.12, 6.05, 5.93, and 5.83, respectively. Horizontal bars in panels A and C represent the marker used to calculate mean values of G0/G1 peak cell populations. PCNA indicates proliferating cell nuclear antigen.

Increased posttranslational modification of p27kip1 correlates with cell-cycle entry. FACS analysis shows the percentage of cells arrested in G1/G0 (A, left panel) in primary B cells with or without treatment with PMA for 72 hours (labeled as primary B or primary B + PMA, respectively), Burkitt lymphoma cell line BL40 (labeled as BL40), (C) in H1299 cells with or without the inducible expression of p27kip1 (labeled as H1299, H1299 + p27kip1) and in Cal51 cells. Right-hand panels of A and C are Western blots showing the expression levels of p27kip1 in the corresponding cell populations used to carry out the FACS and 2D gel analysis. The isoforms 1 to 7 are indicated with arrows in panels B and D and their isoelectric points are 6.76, 6.59, 6.37, 6.12, 6.05, 5.93, and 5.83, respectively. Horizontal bars in panels A and C represent the marker used to calculate mean values of G0/G1 peak cell populations. PCNA indicates proliferating cell nuclear antigen.

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