Fig. 3.
Fig. 3. p53-dependent transcription determined by luciferase activity of reporter plasmid pG13PYluc. / (A) Jurkat cells stably expressing ZEBRA (Z+) and control cells (Z−) were transiently transfected with 200 ng of reporter plasmids (pG13PYluc or pGM15PYluc) and with 500 ng of p53 expression plasmids for either p53W or p53C. Significant transcription activation was detected with pG13PYluc reporter, but not with mutated pGM15PYluc reporter in Z+ cells with cotransfection of 53W (*P < .05) or 53C (**P < .05). In the absence of cotransfected p53, transcription of p53 reporter genes was extremely low in both Z+ and Z− cells. (B) Parental Jurkat cells were transiently transfected with ZEBRA (500 ng) and p53 expression plasmids (500 ng) with reporter plasmids (200 ng). Transcription of pG13PYluc with cotransfection of p53W was slightly increased by transient cotransfection of pSV2-neo-WZhet ZEBRA expression plasmid (Z+) compared to transient transfection of control plasmid pSV2-neo (Z−), but this increase was not significant (P > .05) in pooled experimental data. Transcription of mutated pGM15PYluc reporter was not activated by transient transfection of either p53 or ZEBRA.

p53-dependent transcription determined by luciferase activity of reporter plasmid pG13PYluc.

(A) Jurkat cells stably expressing ZEBRA (Z+) and control cells (Z−) were transiently transfected with 200 ng of reporter plasmids (pG13PYluc or pGM15PYluc) and with 500 ng of p53 expression plasmids for either p53W or p53C. Significant transcription activation was detected with pG13PYluc reporter, but not with mutated pGM15PYluc reporter in Z+ cells with cotransfection of 53W (*P < .05) or 53C (**P < .05). In the absence of cotransfected p53, transcription of p53 reporter genes was extremely low in both Z+ and Z− cells. (B) Parental Jurkat cells were transiently transfected with ZEBRA (500 ng) and p53 expression plasmids (500 ng) with reporter plasmids (200 ng). Transcription of pG13PYluc with cotransfection of p53W was slightly increased by transient cotransfection of pSV2-neo-WZhet ZEBRA expression plasmid (Z+) compared to transient transfection of control plasmid pSV2-neo (Z−), but this increase was not significant (P > .05) in pooled experimental data. Transcription of mutated pGM15PYluc reporter was not activated by transient transfection of either p53 or ZEBRA.

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