ALTERNATIVELY SPLICED P53-RNA IN TRANSFORMED AND NORMAL-CELLS OF DIFFERENT TISSUE TYPES

被引:58
作者
HAN, KA
KULESZMARTIN, MF
机构
[1] ROSWELL PK CANC INST,GRACE CANC DRUG CTR,PROGRAM BIOCHEM,BUFFALO,NY 14263
[2] ROSWELL PK CANC INST,GRACE CANC DRUG CTR,DEPT EXPTL THERAPEUT,BUFFALO,NY 14263
关键词
D O I
10.1093/nar/20.8.1979
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 alternatively spliced RNA species of tumor suppressor gene p53, containing an additional 96 bases derived from intron 10, is present at approximately 25 to 30% the level of regularly spliced p53 RNA in both normal epidermal and carcinoma cells. The presence of this alternatively spliced RNA in 10T1/2 fibroblast cells, mouse liver and testis suggests that this alternative splicing may be universal. The level of alternatively spliced p53 RNA was increased coordinately with that of regularly spliced p53 in 10T1/2 cells in response to epidermal growth factor. Immunoprecipitation analysis of epidermal cells using monoclonal antibodies which recognize different epitopes of p53 suggested that distinct p53 proteins may be translated from both RNA species. Considering previous observations on the potential importance of carboxyl terminal sequences in p53 function, knowledge of the ubiquitous presence of alternatively spliced p53 is important for future studies of p53 function in normal cells and in oncogenesis.
引用
收藏
页码:1979 / 1981
页数:3
相关论文
共 20 条
[1]   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
[2]   EVIDENCE FOR ALLOSTERIC VARIANTS OF WILD-TYPE-P53, A TUMOR SUPPRESSOR PROTEIN [J].
COOK, A ;
MILNER, J .
BRITISH JOURNAL OF CANCER, 1990, 61 (04) :548-552
[3]   TRANSFORMING GROWTH-FACTOR ALPHA (TGF-ALPHA) INDUCTION OF C-FOS AND C-MYC EXPRESSION IN C3H 1OT1/2 CELLS [J].
CUTRY, AF ;
KINNIBURGH, AJ ;
TWARDZIK, DR ;
WENNER, CE .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 152 (01) :216-222
[4]  
GILMAN M, 1989, CURRENT PROTOCOLS MO, V1
[5]  
GINSBERG D, 1990, ONCOGENE, V5, P1285
[6]   ALTERED LEVELS OF ENDOGENOUS RETROVIRUS-LIKE SEQUENCE (VL30) RNA DURING MOUSE EPIDERMAL-CELL CARCINOGENESIS [J].
HAN, KA ;
ROTHBERG, P ;
KULESZMARTIN, M .
MOLECULAR CARCINOGENESIS, 1990, 3 (02) :75-82
[7]  
HAN KA, 1992, CANCER RES, V2, P749
[8]  
HEROLD KM, 1988, ONCOGENE, V3, P423
[9]  
KAWASKAI ES, 1990, PCR PROTOCOLS GUIDE, P23
[10]   MOUSE-CELL CLONES FOR IMPROVED QUANTITATION OF CARCINOGEN-INDUCED ALTERED DIFFERENTIATION [J].
KULESZMARTIN, M ;
YOSHIDA, MA ;
PRESTINE, L ;
YUSPA, SH ;
BERTRAM, JS .
CARCINOGENESIS, 1985, 6 (09) :1245-1254