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Differential regulation of transcription and induction of programmed cell death by human p53‐family members p63 and p73
Author(s) -
Dietz Sebastian,
Rother Karen,
Bamberger Casimir,
Schmale Hartwig,
Mössner Joachim,
Engeland Kurt
Publication year - 2002
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/s0014-5793(02)03093-4
Subject(s) - programmed cell death , microbiology and biotechnology , transcription (linguistics) , transcription factor , human cell , biology , chemistry , apoptosis , genetics , cell culture , gene , philosophy , linguistics
The p53 tumor suppressor acts as a transcription factor and has a central function in controlling apoptosis. With p63 and p73 two genes coding for proteins homologous to p53 have been identified. We describe the properties of seven human p63 and p73 proteins as transcriptional activators of p21WAF1 / CIP1 expression and apoptotic inducers in direct comparison to p53 in the same assay systems employing DLD‐1‐tet‐off colon cells. Programmed cell death is detected in cells expressing high levels of p53 and p73α. Cells overexpressing TAp63α, TAp63γ, TA*p63α, TA*p63γ, ΔNp63α, and ΔNp63γ display low or no detectable apoptosis.