CHEMICALLY ALTERED APURINIC SITES IN PHI-X174 DNA GIVE INCREASED MUTAGENESIS IN SOS-INDUCED ESCHERICHIA-COLI

被引:6
作者
BOCKRATH, R [1 ]
KOW, YW [1 ]
WALLACE, SS [1 ]
机构
[1] UNIV VERMONT,MARKEY CTR MOLEC GENET,DEPT MICROBIOL & MOLEC GENET,BURLINGTON,VT 05405
来源
MUTATION RESEARCH | 1993年 / 288卷 / 02期
关键词
APURINIC DNA DAMAGE; SOS MUTAGENESIS; TRANSLESION SYNTHESIS; ELECTROPORATION;
D O I
10.1016/0027-5107(93)90086-U
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Single-strand DNA from bacteriophage (PHIX174 am3 is treated with mild acid and heat to produce increasing numbers of apurinic sites per molecule. Samples are assayed, either directly or after additional chemical reactions, by electroporation into the recipient E. coli strain HF4714(su-1+). Modified apurinic sites are produced by reactions with 0-methyl- or 0-benzyl-hydroxylamine, and reduced apurinic sites by reactions with sodium borohydride. Reversion mutation frequencies are significant only if the recipient strain is SOS-induced (by growth after UV irradiation). A simple apurinic site at the target gives rise to mutation (a transversion) with a probability of 0.07, while the modified or reduced apurinic site has a mutagenic efficiency of 0.22-0.27 or 0.29, respectively. The open ring form of deoxyribose may account for the 3-4-fold increased mutagenicity with altered apurinic lesions. Also considered are effects by temperature and cyclobutane pyrimidine dimers on mutagenicity and the relatively invariant survival curves that obtain regardless of chemical alterations at the apurinic sites and/or SOS induction.
引用
收藏
页码:207 / 214
页数:8
相关论文
共 24 条
[1]   SOS-DEPENDENT REPLICATION PAST A SINGLE TRANS-SYN T-T CYCLOBUTANE DIMER GIVES A DIFFERENT MUTATION SPECTRUM AND INCREASED ERROR RATE COMPARED WITH REPLICATION PAST THIS LESION IN UNINDUCED CELLS [J].
BANERJEE, SK ;
BORDEN, A ;
CHRISTENSEN, RB ;
LECLERC, JE ;
LAWRENCE, CW .
JOURNAL OF BACTERIOLOGY, 1990, 172 (04) :2105-2112
[2]   ANTI-MUTAGENIC EFFECT OF ULTRAVIOLET-LIGHT ON SPONTANEOUS TYROSINE TRANSFER-RNA OCHRE SUPPRESSOR MUTATIONS IN ESCHERICHIA-COLI [J].
BOCKRATH, R ;
RUIZRUBIO, M .
MOLECULAR & GENERAL GENETICS, 1988, 214 (02) :361-364
[3]   CODING PROPERTIES OF POLY(DEOXYCYTIDYLIC ACID) TEMPLATES CONTAINING URACIL OR APYRIMIDINIC SITES - INVITRO MODULATION OF MUTAGENESIS BY DEOXYRIBONUCLEIC-ACID REPAIR ENZYMES [J].
BOITEUX, S ;
LAVAL, J .
BIOCHEMISTRY, 1982, 21 (26) :6746-6751
[4]   ESTIMATION OF APURINIC-APYRIMIDINIC SITES AND PHOSPHOTRIESTERS IN DEOXYRIBONUCLEIC-ACID TREATED WITH ELECTROPHILIC CARCINOGENS AND MUTAGENS [J].
DRINKWATER, NR ;
MILLER, EC ;
MILLER, JA .
BIOCHEMISTRY, 1980, 19 (22) :5087-5092
[5]   COCRYSTAL STRUCTURE OF AN EDITING COMPLEX OF KLENOW FRAGMENT WITH DNA [J].
FREEMONT, PS ;
FRIEDMAN, JM ;
BEESE, LS ;
SANDERSON, MR ;
STEITZ, TA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :8924-8928
[6]  
HIGGINS CF, 1990, BACTERIAL CHROMOSOME, P421
[7]   3-DIMENSIONAL STRUCTURE OF THE BETA-SUBUNIT OF ESCHERICHIA-COLI DNA POLYMERASE-III HOLOENZYME - A SLIDING DNA CLAMP [J].
KONG, XP ;
ONRUST, R ;
ODONNELL, M ;
KURIYAN, J .
CELL, 1992, 69 (03) :425-437
[8]   MECHANISM OF ACTION OF ESCHERICHIA-COLI EXONUCLEASE-III [J].
KOW, YW .
BIOCHEMISTRY, 1989, 28 (08) :3280-3287
[9]   MUTATIONAL SPECIFICITY OF DEPURINATION [J].
KUNKEL, TA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (05) :1494-1498
[10]  
KUNKEL TA, 1986, J BIOL CHEM, V261, P160