INVIVO FATE OF MMS-INDUCED DNA LESIONS THAT ELICIT SCE

被引:7
作者
MORALESRAMIREZ, P
RODRIGUEZREYES, R
VALLARINOKELLY, T
机构
[1] Departamento de Radiobiología, Instituto Nacional de Investigaciones Nucleares, Mexico, D.F.
来源
MUTATION RESEARCH | 1992年 / 272卷 / 03期
关键词
SISTER-CHROMATID EXCHANGE; METHYL METHANESULFONATE; 3-WAY DIFFERENTIAL STAINING;
D O I
10.1016/0165-1161(92)91534-X
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A previously reported in vivo protocol, which uses three-way differential staining (TWD) of sister chromatids, allows the screening of mutagen-induced sister-chromatid exchange (SCE) in each of the two cell divisions after mutagen treatment and also those occurring at apparently the same locus in both divisions. In the present work the effect of methyl methanesulfonate (MMS) was studied by means of this protocol. The results showed that MMS-induced DNA lesions that cause SCE are persistent. Some lesions were induced in the second division, as was inferred from the analysis of the response in single cells. The data also indicate that bromodeoxyuridine reduces DNA sensitivity to SCE induction by MMS.
引用
收藏
页码:215 / 221
页数:7
相关论文
共 24 条
[1]   DNA CROSSLINKING, SISTER-CHROMATID EXCHANGE AND SPECIFIC-LOCUS MUTATIONS [J].
CARRANO, AV ;
THOMPSON, LH ;
STETKA, DG ;
MINKLER, JL ;
MAZRIMAS, JA ;
FONG, S .
MUTATION RESEARCH, 1979, 63 (01) :175-188
[2]   RELATIONSHIP BETWEEN DNA ADDUCT FORMATION AND SISTER CHROMATID EXCHANGE INDUCTION BY [8-METHOXYPSORALEN-H-3 IN CHINESE-HAMSTER OVARY CELLS [J].
CASSEL, DM ;
LATT, SA .
EXPERIMENTAL CELL RESEARCH, 1980, 128 (01) :15-22
[3]   SIMPLE DIFFERENTIAL GIEMSA STAINING OF SISTER CHROMATIDS AFTER TREATMENT WITH PHOTOSENSITIVE DYES AND EXPOSURE TO LIGHT AND MECHANISM OF STAINING [J].
GOTO, K ;
AKEMATSU, T ;
SHIMAZU, H ;
SUGIYAMA, T .
CHROMOSOMA, 1975, 53 (03) :223-230
[4]   EFFECTS OF INHIBITORS OF DNA-SYNTHESIS ON SPONTANEOUS AND ULTRAVIOLET LIGHT-INDUCED SISTER-CHROMATID EXCHANGES IN CHINESE-HAMSTER CELLS [J].
ISHII, Y ;
BENDER, MA .
MUTATION RESEARCH, 1980, 79 (01) :19-32
[5]   NATURE OF THE MITOMYCIN-C INDUCED LESION CAUSING SISTER-CHROMATID EXCHANGE [J].
ISHII, Y .
MUTATION RESEARCH, 1981, 91 (01) :51-55
[6]   DYSKERATOSIS CONGENITA - SURVIVAL, SISTER-CHROMATID EXCHANGE AND REPAIR FOLLOWING TREATMENTS WITH CROSSLINKING AGENTS [J].
KANO, Y ;
FUJIWARA, Y .
MUTATION RESEARCH, 1982, 103 (3-6) :327-332
[7]   EVIDENCE THAT THE REPLICATION POINT IS THE SITE OF SISTER CHROMATID EXCHANGE [J].
KATO, H .
CANCER GENETICS AND CYTOGENETICS, 1980, 2 (01) :69-77
[8]   EFFECT OF SERA ON SISTER CHROMATID EXCHANGES INVITRO [J].
KATO, H ;
SANDBERG, AA .
EXPERIMENTAL CELL RESEARCH, 1977, 109 (02) :445-448
[9]   FATE OF UV-INDUCED LESIONS AFFECTING SCES, CHROMOSOME ABERRATIONS AND SURVIVAL OF CHO CELLS ARRESTED BY DEPRIVATION OF ARGININE [J].
MACRAE, WD ;
MACKINNON, EA ;
STICH, HF .
CHROMOSOMA, 1979, 72 (01) :15-22
[10]   CHEMICAL CARCINOGENESIS IN NERVOUS-SYSTEM - PREFERENTIAL ACCUMULATION OF O6-METHYLGUANINE IN RAT-BRAIN DEOXYRIBONUCLEIC-ACID DURING REPETITIVE ADMINISTRATION OF N-METHYL-N-NITROSOUREA [J].
MARGISON, GP ;
KLEIHUES, P .
BIOCHEMICAL JOURNAL, 1975, 148 (03) :521-525