The C-terminus of mutant p53 is necessary for its ability to interfere with growth arrest or apoptosis

被引:12
作者
Sigal, A [1 ]
Matas, D [1 ]
Almog, N [1 ]
Goldfinger, N [1 ]
Rotter, V [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
关键词
mutant p53; gain of function; apoptosis; growth arrest; G(2);
D O I
10.1038/sj.onc.1204724
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ability to suppress wild type p53-independent apoptosis may play an important role in the oncogenicity of p53 mutant proteins. However, structural elements necessary for this activity are unknown. Furthermore, it is unclear whether this mutant p53 mediated inhibition is specific to the apoptotic pathway or a more general suppression of the cellular response to stress. We observed that an unmodified C-terminus was required for the suppression of apoptosis by the p53 135(Ala to Val) oncogenic p53 mutant. It was also required for the novel activity of G(2) arrest suppression, the predominant response at low levels of genotoxic stress. These observations are consistent with a model whereby mutant p53 suppressive activity is not specific to the apoptotic pathway, but rather increases the threshold of genotoxic stress needed for a DNA damage response to occur. Furthermore, these observations indicate that it may be possible to selectively kill mutant p53 expressing cells based on the lower sensitivity of their growth arrest response.
引用
收藏
页码:4891 / 4898
页数:8
相关论文
共 61 条
[1]  
Agami R, 1999, NATURE, V399, P809
[2]   The murine C'-terminally alternatively spliced form of p53 induces attenuated apoptosis in myeloid cells [J].
Almog, N ;
Li, RZ ;
Peled, A ;
Schwartz, D ;
Wolkowicz, R ;
Goldfinger, N ;
Pei, HP ;
Rotter, V .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (02) :713-722
[3]   p53-dependent apoptosis is regulated by a C-terminally alternatively spliced form of murine p53 [J].
Almog, N ;
Goldfinger, N ;
Rotter, V .
ONCOGENE, 2000, 19 (30) :3395-3403
[4]   ACCUMULATION OF WILD-TYPE P53 PROTEIN UPON GAMMA-IRRADIATION INDUCES A G(2) ARREST-DEPENDENT IMMUNOGLOBULIN-KAPPA LIGHT-CHAIN GENE-EXPRESSION [J].
ALONIGRINSTEIN, R ;
SCHWARTZ, D ;
ROTTER, V .
EMBO JOURNAL, 1995, 14 (07) :1392-1401
[5]   Reciprocal interference between the sequence-specific core and nonspecific C-terminal DNA binding domains of p53: Implications for regulation [J].
Anderson, ME ;
Woelker, B ;
Reed, M ;
Wang, P ;
Tegtmeyer, P .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (11) :6255-6264
[6]   IMMUNOLOGICALLY DISTINCT P53 MOLECULES GENERATED BY ALTERNATIVE SPLICING [J].
ARAI, N ;
NOMURA, D ;
YOKOTA, K ;
WOLF, D ;
BRILL, E ;
SHOHAT, O ;
ROTTER, V .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (09) :3232-3239
[7]   Pretreatment with DNA-damaging agents permits selective killing of checkpoint-deficient cells by microtubule-active drugs [J].
Blagosklonny, MV ;
Robey, R ;
Bates, S ;
Fojo, T .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (04) :533-539
[8]  
Blagosklonny MV, 2000, CANCER RES, V60, P3425
[9]   Mutant p53 gain of function: differential effects of different p53 mutants on resistance of cultured cells to chemotherapy [J].
Blandino, G ;
Levine, AJ ;
Oren, M .
ONCOGENE, 1999, 18 (02) :477-485
[10]   14-3-3σ is required to prevent mitotic catastrophe after DNA damage [J].
Chan, TA ;
Hermeking, H ;
Lengauer, C ;
Kinzler, KW ;
Vogelstein, B .
NATURE, 1999, 401 (6753) :616-620