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Mol Cell Biol, July 1998, p. 3692-3698, Vol. 18, No. 7
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Characterization of Structural p53 Mutants Which
Show Selective Defects in Apoptosis but Not Cell Cycle Arrest
Kevin M.
Ryan and
Karen H.
Vousden*
ABL Basic Research Program, NCI-FCRDC,
Frederick, Maryland 21702
Received 24 November 1997/Returned for modification 5 January
1998/Accepted 8 April 1998
Suppression of tumor cell growth by p53 results from the activation
of both apoptosis and cell cycle arrest, functions which have been
shown to be separable activities of p53. We have characterized a series
of p53 mutants with amino acid substitutions at residue 175 and show
that these mutants fall into one of three classes: class I, which is
essentially wild type for apoptotic and cell cycle arrest functions;
class II, which retains cell cycle arrest activity but is impaired in
the induction of apoptosis; and class III, which is defective in both
activities. Several residue 175 mutants which retain cell cycle arrest
function have been detected in cancers, and we show that these have
lost apoptotic function. Furthermore, several class II mutants have
been found to be temperature sensitive for apoptotic activity while
showing constitutive cell cycle arrest function. Taken together, these
mutants comprise an excellent system with which to investigate the
biochemical nature of p53-mediated apoptosis, the function of principal
importance in tumor suppression. All of the mutants that showed loss of
apoptotic function also showed defects in the activation of promoters
from the potential apoptotic targets Bax and the
insulin-like growth factor-binding protein 3 gene
(IGF-BP3), and a correlation between full apoptotic
activity and activation of both of these promoters was also seen with
the temperature-sensitive mutants. However, a role for additional
apoptotic activities of p53 was suggested by the observation that some
mutants retained significant apoptotic function despite being impaired
in the activation of Bax- and IGF-BP3-derived
promoters. In contrast to the case of transcriptional activation, a
perfect correlation between transcriptional repression of the
c-fos promoter and the ability to induce apoptosis was seen, although the observation that Bax expression induced a similar repression of transcription from this promoter suggests that this may
be a consequence, rather than a cause, of apoptotic death.
*
Corresponding author. Mailing address: ABL Basic
Research Program, NCI-FCRDC, Building 560, Room 22-96, West 7th St.,
Frederick, MD 21702-1201. Phone: (301) 846-1726. Fax: (301) 846-1666. E-mail: vousden{at}ncifcrf.gov.
Mol Cell Biol, July 1998, p. 3692-3698, Vol. 18, No. 7
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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