The "A" rule revisited: polymerases as determinants of mutational specificity

被引:90
作者
Strauss, BS [1 ]
机构
[1] Univ Chicago, Dept Mol Genet & Cell Biol, Chicago, IL 60637 USA
关键词
DNA polymerase; mutation; mismatch repair; frameshift; proofreading;
D O I
10.1016/S1568-7864(01)00014-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Organisms control the specificity and frequency with which they mutate via their complement of proteins. The mismatch repair (MMR) proteins correct errors after they are made. The DNA polymerases of the cell determine the response to damaged DNA which has not been repaired by excision. Polymerase action can be considered as consisting of three main steps: addition of a base, proofreading of the added nucleotide and elongation. Each of these steps is kinetically complex and can be modulated. The modulation accounts for different behaviors of organisms in response to stress. The recent findings of DNA polymerases with properties appropriate for dealing with damaged DNA may help to account for the phenomenon of spontaneous mutation and for the hypermutability associated with immunoglobulin maturation and carcinogenesis. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:125 / 135
页数:11
相关论文
共 82 条
[1]   5′-Deoxyribose phosphate lyase activity of human DNA polymerase ι in vitro [J].
Bebenek, K ;
Tissier, A ;
Frank, EG ;
McDonald, JP ;
Prasad, R ;
Wilson, SH ;
Woodgate, R ;
Kunkel, TA .
SCIENCE, 2001, 291 (5511) :2156-2159
[2]   MUTAGENESIS BY ALKYLATING-AGENTS - CODING PROPERTIES FOR DNA-POLYMERASE OF POLY (DC) TEMPLATE CONTAINING 3-METHYLCYTOSINE [J].
BOITEUX, S ;
LAVAL, J .
BIOCHIMIE, 1982, 64 (8-9) :637-641
[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]  
BOOSALIS MS, 1989, J BIOL CHEM, V264, P11360
[5]   Hypermutation in pathogenic bacteria: Frequent phase variation in meningococci is a phenotypic trait of a specialized mutator biotype [J].
Bucci, C ;
Lavitola, A ;
Salvatore, P ;
Del Giudice, L ;
Massardo, DR ;
Bruni, CB ;
Alifano, P .
MOLECULAR CELL, 1999, 3 (04) :435-445
[6]   Stationary-phase mutation in the bacterial chromosome: Recombination protein and DNA polymerase IV dependence [J].
Bull, HJ ;
Lombardo, MJ ;
Rosenberg, SM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (15) :8334-8341
[7]   Historical overview: Searching for replication help in all of the rec places [J].
Cox, MM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (15) :8173-8180
[8]   THE ABASIC SITE AS A CHALLENGE TO DNA-POLYMERASE - A NUCLEAR-MAGNETIC-RESONANCE STUDY OF G, C AND T OPPOSITE A MODEL ABASIC SITE [J].
CUNIASSE, P ;
FAZAKERLEY, GV ;
GUSCHLBAUER, W ;
KAPLAN, BE ;
SOWERS, LC .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 213 (02) :303-314
[9]   Decreased frequency of somatic hypermutation and impaired affinity maturation but intact germinal center formation in mice expressing antisense RNA to DNA polymerase ζ [J].
Diaz, M ;
Verkoczy, LK ;
Flajnik, MF ;
Klinman, NR .
JOURNAL OF IMMUNOLOGY, 2001, 167 (01) :327-335
[10]  
Foster PL, 1998, GENETICS, V148, P1453