THE ROLE OF EXCISION REPAIR IN THE REMOVAL OF TRANSIENT BENZO[A]PYRENE-INDUCED DNA LESIONS IN CHINESE HAMSTER OVARY CELLS

被引:13
作者
BLAKEY, DH
DOUGLAS, GR
机构
[1] Mutagenesis Section, Environmental Health Directorate, Department of National Health and Welfare, Ottawa
来源
MUTATION RESEARCH | 1990年 / 236卷 / 01期
关键词
ASG sites; Benzo[a]pyrene; CHO cells; Excision repair;
D O I
10.1016/0921-8777(90)90030-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In Chinese hamster ovary (CHO) cells, benzo[a]pyrene induces both persistent and transient lesions that are detected by alkaline sucrose gradient sedimentation analysis (ASG sites). The transient lesions disappear within 15 min while the persistent lesions can be detected for several hours following treatment. Although the persistent ASG sites are believed to be repaired by excision repair, the process responsible for the disappearance of the transient ASG sites is unknown. To determine the contribution of excision repair to the removal of these transient lesions, CHO cells were treated with benzo[a]pyrene (B(a)P) in the presence of the inhibitors of excision repair, araC and novobiocin. The results indicate that: (1) araC inhibits the removal of persistent, but not the transient B(a)P-induced ASG sites; (2) novobiocin, a putative inhibitor of the incision step of DNA excision repair, reduced the number of lesions detected immediately following treatment, indicating that many of these lesions may represent single-strand discontinuities generated during repair; and (3) the lesions detected in the presence of novobiocin disappear rapidly following treatment. Based on these results, we concluded that B(a)P-induced transient ASG sites are repaired by a process other than excision repair. © 1990.
引用
收藏
页码:35 / 41
页数:7
相关论文
共 31 条
[1]   MOLECULAR DOSIMETRY OF DNA DAMAGE CAUSED BY ALKYLATION .1. SINGLE-STRAND BREAKS INDUCED BY ETHYLATING AGENTS IN CULTURED MAMMALIAN-CELLS IN RELATION TO SURVIVAL [J].
ABBONDANDOLO, A ;
DOGLIOTTI, E ;
LOHMAN, PHM ;
BERENDS, F .
MUTATION RESEARCH, 1982, 92 (1-2) :361-377
[2]   METHODS FOR DETECTING CARCINOGENS AND MUTAGENS WITH SALMONELLA-MAMMALIAN-MICROSOME MUTAGENICITY TEST [J].
AMES, BN ;
MCCANN, J ;
YAMASAKI, E .
MUTATION RESEARCH, 1975, 31 (06) :347-363
[3]   ALKYLATION OF PHOSPHATES AND STABILITY OF PHOSPHATE TRIESTERS IN DNA [J].
BANNON, P ;
VERLY, W .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1972, 31 (01) :103-&
[4]   TRANSIENT DNA LESIONS INDUCED BY BENZO-[ALPHA]PYRENE IN CHINESE-HAMSTER OVARY CELLS [J].
BLAKEY, DH ;
DOUGLAS, GR .
MUTATION RESEARCH, 1984, 140 (2-3) :141-145
[5]  
BLAKEY DH, 1982, ENVIRON MUTAGEN, V4, P404
[6]   THE EFFECT OF VARIOUS INHIBITORS OF DNA-SYNTHESIS ON THE REPAIR OF DNA PHOTOPRODUCTS [J].
CLARKSON, JM ;
MITCHELL, DL .
BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 740 (04) :355-361
[7]   SPECIFICITY AND COMPLETENESS OF INHIBITION OF DNA-REPAIR BY NOVOBIOCIN AND APHIDICOLIN [J].
CLEAVER, JE .
CARCINOGENESIS, 1982, 3 (10) :1171-1174
[8]   NOVOBIOCIN - INHIBITOR OF THE REPAIR OF UV-INDUCED BUT NOT X-RAY-INDUCED DAMAGE IN MAMMALIAN-CELLS [J].
COLLINS, A ;
JOHNSON, R .
NUCLEIC ACIDS RESEARCH, 1979, 7 (05) :1311-1320
[9]   THE TIME COURSE OF REPAIR OF ULTRAVIOLET-INDUCED DNA DAMAGE - IMPLICATIONS FOR THE STRUCTURAL ORGANIZATION OF REPAIR [J].
COLLINS, A ;
SQUIRES, S .
MUTATION RESEARCH, 1986, 166 (01) :113-119