All three SOS-inducible DNA polymerases (Pol II, Pol IV and Pol V) are involved in induced mutagenesis

被引:303
作者
Napolitano, R
Janel-Bintz, R
Wagner, J
Fuchs, RPP [1 ]
机构
[1] ESBS, CNRS Cancerogenese & Mutagenese Mol & Struct, UPR 9003, Strasbourg, France
[2] IRCAD, Strasbourg, France
关键词
chemical carcinogens; DNA polymerases; frameshift mutagenesis; NarI mutation hot spot; slippage mutagenesis;
D O I
10.1093/emboj/19.22.6259
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
Most organisms contain several members of a recently discovered class of DNA polymerases (umuC/dinB superfamily) potentially involved in replication of damaged DNA, In Escherichia coli, only Pol V (umuDC) was known to be essential for base substitution mutagenesis induced by UV light or abasic sites. Here we show that, depending upon the nature of the DNA damage and its sequence context, the two additional SOS-inducible DNA polymerases, Pol II (polB) and Pol IV (dinB), are also involved in error-free and mutagenic translesion synthesis (TLS). For example, bypass of N-2-acetylaminofluorene (AAF) guanine adducts located within the NarI mutation hot spot requires Pol II for -2 frameshifts but Pol V for error-free TLS, On the other hand, error-free and -1 frameshift TLS at a benzo(a)pyrene adduct requires both Pol IV and Pol V, Therefore, in response to the vast diversity of existing DNA damage, the cell uses a pool of 'translesional' DNA polymerases in order to bypass the various DNA lesions.
引用
收藏
页码:6259 / 6265
页数:7
相关论文
共 52 条
[1]  
[Anonymous], 1983, MOL BIOL MUTAGENS CA
[2]  
BACHERREUVEN N, 1999, J BIOL CHEM, V274, P31763
[3]   SOS mutagenesis results from up-regulation of translesion synthesis [J].
Becherel, OJ ;
Fuchs, RPP .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 294 (02) :299-306
[4]   DNA polymerase II (polB) is involved in a new DNA repair pathway for DNA interstrand cross-links in Escherichia coli [J].
Berardini, M ;
Foster, PL ;
Loechler, EL .
JOURNAL OF BACTERIOLOGY, 1999, 181 (09) :2878-2882
[5]  
BONNER CA, 1988, J BIOL CHEM, V263, P18946
[6]   Sequence-dependent modulation of frameshift mutagenesis at NarI-derived mutation hot spots [J].
Broschard, TH ;
Koffel-Schwartz, N ;
Fuchs, RPP .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 288 (01) :191-199
[7]   ROLE OF RECA PROTEIN IN UNTARGETED UV MUTAGENESIS OF BACTERIOPHAGE-LAMBDA - EVIDENCE FOR THE REQUIREMENT FOR THE DINB GENE [J].
BROTCORNELANNOYE, A ;
MAENHAUTMICHEL, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (11) :3904-3908
[8]   SINGLE ADDUCT MUTAGENESIS - STRONG EFFECT OF THE POSITION OF A SINGLE ACETYLAMINOFLUORENE ADDUCT WITHIN A MUTATION HOT SPOT [J].
BURNOUF, D ;
KOEHL, P ;
FUCHS, RPP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (11) :4147-4151
[9]   PURIFICATION AND PROPERTIES OF WILD-TYPE AND EXONUCLEASE-DEFICIENT DNA-POLYMERASE-II FROM ESCHERICHIA-COLI [J].
CAI, H ;
YU, H ;
MCENTEE, K ;
KUNKEL, TA ;
GOODMAN, MF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (25) :15327-15335
[10]   Replication of damaged DNA: molecular defect in Xeroderma pigmentosum variant cells [J].
Cordonnier, AM ;
Fuchs, RPP .
MUTATION RESEARCH-DNA REPAIR, 1999, 435 (02) :111-119