THE EMERGING PICTURE OF P53

被引:57
作者
SELTER, H
MONTENARH, M
机构
来源
INTERNATIONAL JOURNAL OF BIOCHEMISTRY | 1994年 / 26卷 / 02期
关键词
D O I
10.1016/0020-711X(94)90139-2
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
1. The cellular phosphoprotein p53 is a negative regulator of the cell growth. A great majority of human malignancies expresses a mutated p53 that represents an oncogenic version of the protein. 2. However, in the meantime many tumors were identified containing a p53 protein without any mutation. Here also other events than genomic alterations of p53 might be implicated in the process of cell transformation. 3. The expression of wild-type or mutant conformation is not exclusively defined by the p53 DNA sequence but also influenced by the subcellular environment and the interaction of cellular proteins with p53. 4. In particular, the mdm-2 gene product appears to be an important partner of p53 somehow involved in these complex regulatory processes. 5. Recent findings supported a role for p53 in transcriptional regulation, perhaps by reducing the expression of genes that are needed for ongoing cell proliferation. 6. This property may be based upon the ability of p53 to bind DNA as well as different proteins from viral or cellular origin. 7. Especially transcription factors or further cellular proteins connected in any way with the regulation of cell proliferation are possible candidates. 8. Thus, it is not surprising that p53 is implicated in the regulation of the cell cycle and in the decision of a cell to replicate DNA or to go into apoptosis.
引用
收藏
页码:145 / 154
页数:10
相关论文
共 132 条
[91]   THE MDM-2 ONCOGENE PRODUCT FORMS A COMPLEX WITH THE P53 PROTEIN AND INHIBITS P53-MEDIATED TRANSACTIVATION [J].
MOMAND, J ;
ZAMBETTI, GP ;
OLSON, DC ;
GEORGE, D ;
LEVINE, AJ .
CELL, 1992, 69 (07) :1237-1245
[92]   DIMERS AND COMPLEXES WITH P53 ARE THE PREVALENT OLIGOMERIC FORMS OF A TRANSFORMING NONKARYOPHILIC T-ANTIGEN OF SIMIAN VIRUS-40 [J].
MONTENARH, M ;
VESCO, C ;
SCHEIDTMANN, KH .
JOURNAL OF VIROLOGY, 1987, 61 (03) :940-944
[93]   HUMAN P53 AND CDC2HS GENES COMBINE TO INHIBIT THE PROLIFERATION OF SACCHAROMYCES-CEREVISIAE [J].
NIGRO, JM ;
SIKORSKI, R ;
REED, SI ;
VOGELSTEIN, B .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (03) :1357-1365
[94]   P53-CATALYZED ANNEALING OF COMPLEMENTARY SINGLE-STRANDED NUCLEIC-ACIDS [J].
OBEROSLER, P ;
HLOCH, P ;
RAMSPERGER, U ;
STAHL, H .
EMBO JOURNAL, 1993, 12 (06) :2389-2396
[95]   ONCOPROTEIN MDM2 CONCEALS THE ACTIVATION DOMAIN OF TUMOR SUPPRESSOR-P53 [J].
OLINER, JD ;
PIETENPOL, JA ;
THIAGALINGAM, S ;
GVURIS, J ;
KINZLER, KW ;
VOGELSTEIN, B .
NATURE, 1993, 362 (6423) :857-860
[96]   COOPERATION BETWEEN GENE ENCODING P53 TUMOR-ANTIGEN AND RAS IN CELLULAR-TRANSFORMATION [J].
PARADA, LF ;
LAND, H ;
WEINBERG, RA ;
WOLF, D ;
ROTTER, V .
NATURE, 1984, 312 (5995) :649-651
[97]  
REIHSAUS E, 1990, ONCOGENE, V5, P137
[98]   P53 TRANSFORMATION-RELATED PROTEIN ACCUMULATES IN THE NUCLEUS OF TRANSFORMED FIBROBLASTS IN ASSOCIATION WITH THE CHROMATIN AND IS FOUND IN THE CYTOPLASM OF NON-TRANSFORMED FIBROBLASTS [J].
ROTTER, V ;
ABUTBUL, H ;
BENZEEV, A .
EMBO JOURNAL, 1983, 2 (07) :1041-1047
[99]   ANALYSIS OF A PROTEIN-BINDING DOMAIN OF P53 [J].
RUPPERT, JM ;
STILLMAN, B .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (06) :3811-3820
[100]   CELL-CYCLE ANALYSIS OF P53-INDUCED CELL-DEATH IN MURINE ERYTHROLEUKEMIA-CELLS [J].
RYAN, JJ ;
DANISH, R ;
GOTTLIEB, CA ;
CLARKE, MF .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (01) :711-719