Frequency of HPRT gene mutations induced by N-methyl-N′-nitro-N-nitrosoguanidine corresponds to replication error phenotypes of cell lines

被引:11
作者
Zhu, WB [1 ]
Yamasaki, H [1 ]
Mironov, N [1 ]
机构
[1] Int Agcy Res Canc, Unit Multistage Carcinogenesis, F-69372 Lyon 08, France
关键词
HPRT; MNNG; RER; mutation; mismatch repair;
D O I
10.1016/S0027-5107(97)00244-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have examined whether cells with replication error-positive (RER+) and -negative phenotype (RER-) respond differently to the mutagen MNNG, employing three RER+ and two RER- human cell lines. Cells were treated with several concentrations of MNNG, and HPRT mutants were selected phenotypically by their growth in the presence of 6-thioguanine. While the variation of the mutation frequency within each group was about an order of magnitude, it was found that MNNG induced a level of mutations in the HPRT gene some 100- to 1000-fold higher in RER+ cells than in cells with RER- phenotype. MNNG, at a concentration of 30 mu M, produced a mutation frequency 450-fold higher in HCT116 (RER+) cells than in SW480 (RER-) cells. Our findings suggest that the RER+ phenotype predisposes cells to MNNG-induced hypermutability. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:93 / 99
页数:7
相关论文
共 32 条
[1]   CLUES TO THE PATHOGENESIS OF FAMILIAL COLORECTAL-CANCER [J].
AALTONEN, LA ;
PELTOMAKI, P ;
LEACH, FS ;
SISTONEN, P ;
PYLKKANEN, L ;
MECKLIN, JP ;
JARVINEN, H ;
POWELL, SM ;
JEN, J ;
HAMILTON, SR ;
PETERSEN, GM ;
KINZLER, KW ;
VOGELSTEIN, B ;
DELACHAPELLE, A .
SCIENCE, 1993, 260 (5109) :812-816
[2]   hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6 [J].
Acharya, S ;
Wilson, T ;
Gradia, S ;
Kane, MF ;
Guerrette, S ;
Marsischky, GT ;
Kolodner, R ;
Fishel, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :13629-13634
[3]  
Aebi S, 1996, CANCER RES, V56, P3087
[4]   A MISMATCH RECOGNITION DEFECT IN COLON-CARCINOMA CONFERS DNA MICROSATELLITE INSTABILITY AND A MUTATOR PHENOTYPE [J].
AQUILINA, G ;
HESS, P ;
BRANCH, P ;
MACGEOCH, C ;
CASCIANO, I ;
KARRAN, P ;
BIGNAMI, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (19) :8905-8909
[5]  
AQUILINA G, 1995, CANCER RES, V55, P2569
[6]   MOLECULAR ANALYSIS OF MUTATIONS IN MUTATOR COLORECTAL-CARCINOMA CELL-LINES [J].
BHATTACHARYYA, NP ;
GANESH, A ;
PHEAR, G ;
RICHARDS, B ;
SKANDALIS, A ;
MEUTH, M .
HUMAN MOLECULAR GENETICS, 1995, 4 (11) :2057-2064
[7]   MUTATOR PHENOTYPES IN HUMAN COLORECTAL-CARCINOMA CELL-LINES [J].
BHATTACHARYYA, NP ;
SKANDALIS, A ;
GANESH, A ;
GRODEN, J ;
MEUTH, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6319-6323
[8]  
BLACK KA, 1989, AM J PATHOL, V134, P53
[9]  
BRANCH P, 1995, CANCER RES, V55, P2304
[10]   Competency in mismatch repair prohibits clonal expansion of cancer cells treated with N-methyl-N'-nitro-N-nitrosoguanidine [J].
Carethers, JM ;
Hawn, MT ;
Chauhan, DP ;
Luce, MC ;
Marra, G ;
Koi, M ;
Boland, CR .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (01) :199-206