The p53 status of Chinese hamster V79 cells frequently used for studies on DNA damage and DNA repair

被引:88
作者
Chaung, WR
Mi, LJ
Boorstein, RJ
机构
[1] NYU,SCH MED,SACKLER INST GRAD BIOMED SCI,DEPT PATHOL,NEW YORK,NY 10016
[2] RITA & STANLEY KAPLAN CANC CTR,NEW YORK,NY 10016
关键词
MULTIPLE SEQUENCE ALIGNMENT; RADIATION-INDUCED APOPTOSIS; GENE; PROTEIN; EXPRESSION; ANTIGEN; CLONING; MUTAGENESIS; GROWTH;
D O I
10.1093/nar/25.5.992
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
Chinese hamster lung fibroblast V79 cells have been widely used in studies of DNA damage and DNA repair, Since the p53 gene is involved in normal responses to DNA damage, we have analyzed the molecular genetics and functional status of p53 in V79 cells and primary Chinese hamster embryonic fibroblast (CHEF) cells, The coding product of the p53 gene in CHEF cells was 76 and 75% homologous to human and mouse p53 respectively, and was 95% homologous to the Syrian hamster cells, The V79 p53 sequence contained two point mutations located within a presumed DNA binding domain, as compared with the CHEF cells, Additional immunocytochemical and molecular studies confirmed that the p53 protein in V79 cells was mutated and nonfunctional, Our results indicate that caution should be used in interpreting studies of DNA damage, DNA repair and apoptosis in V79 cells.
引用
收藏
页码:992 / 994
页数:3
相关论文
共 32 条
[1]   MOUSE EMBRYO FIBROBLASTS TRANSFORMED BY ACTIVATED RAS OR DOMINANT-NEGATIVE P53 EXPRESS CROSS-REACTIVE TUMOR REJECTION ANTIGENS [J].
APPLEMAN, LJ ;
UYEKI, J ;
FREY, AB .
INTERNATIONAL JOURNAL OF CANCER, 1995, 61 (06) :887-894
[2]   ENHANCED BINDING OF A 95-KDA PROTEIN TO P53 IN CELLS UNDERGOING P53-MEDIATED GROWTH ARREST [J].
BARAK, Y ;
OREN, M .
EMBO JOURNAL, 1992, 11 (06) :2115-2121
[3]  
BOORSTEIN RJ, 1987, CANCER RES, V47, P4372
[4]   A MAMMALIAN-CELL LINE DEFICIENT IN ACTIVITY OF THE DNA-REPAIR ENZYME 5-HYDROXYMETHYLURACIL-DNA GLYCOSYLASE IS RESISTANT TO THE TOXIC EFFECTS OF THE THYMIDINE ANALOG 5-HYDROXYMETHYL-2'-DEOXYURIDINE [J].
BOORSTEIN, RJ ;
CHIU, LN ;
TEEBOR, GW .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (12) :5536-5540
[5]   MUTAGENESIS BY CHEMICAL-AGENTS IN V79 CHINESE-HAMSTER CELLS - A REVIEW AND ANALYSIS OF THE LITERATURE - A REPORT OF THE GENE-TOX PROGRAM [J].
BRADLEY, MO ;
BHUYAN, B ;
FRANCIS, MC ;
LANGENBACH, R ;
PETERSON, A ;
HUBERMAN, E .
MUTATION RESEARCH, 1981, 87 (02) :81-142
[6]   Molecular spectrum of mutations induced by 5-hydroxymethyl-2'-deoxyuridine in (CHO)-PL61 cells [J].
Chaung, WR ;
Boorstein, RJ .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1997, 373 (01) :125-137
[7]   TRANSCRIPTIONAL ACTIVATION BY P53 CORRELATES WITH SUPPRESSION OF GROWTH BUT NOT TRANSFORMATION [J].
CROOK, T ;
MARSTON, NJ ;
SARA, EA ;
VOUSDEN, KH .
CELL, 1994, 79 (05) :817-827
[8]   MOLECULAR-CLONING AND INVITRO EXPRESSION OF A CDNA CLONE FOR HUMAN CELLULAR TUMOR-ANTIGEN P53 [J].
HARLOW, E ;
WILLIAMSON, NM ;
RALSTON, R ;
HELFMAN, DM ;
ADAMS, TE .
MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (07) :1601-1610
[9]  
HIGGINS DG, 1992, COMPUT APPL BIOSCI, V8, P189
[10]   THE REPRODUCTIVE EFFECTS ASSESSMENT GROUPS REVIEW OF THE MUTAGENICITY OF VINYLIDENE-CHLORIDE [J].
JACOBSONKRAM, D .
ENVIRONMENTAL MUTAGENESIS, 1986, 8 (01) :161-169