On the mutagenicity of homologous recombination and double-strand break repair in bacteriophage

被引:1
作者
Shcherbakov, Victor P. [1 ]
Plugina, Lidiya [1 ]
Shcherbakova, Tamara [1 ]
Sizova, Svetlana [1 ]
Kudryashova, Elena [1 ]
机构
[1] RAS, Inst Problems Chem Phys, Chernogolovka 142432, Moscow Region, Russia
关键词
Genetic recombination; Bacteriophage T4; Double-strand break repair; Fidelity; DNA replication; Gene uvsX; 46/47; protein; DEPENDENT DNA-REPLICATION; AFFECTING GENETIC-RECOMBINATION; JOINT MOLECULES; POLYMERASE-ETA; MUTATIONS; PROTEINS; UVSX; MRE11; PURIFICATION; CHECKPOINT;
D O I
10.1016/j.dnarep.2010.09.006
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The double-strand break (DSB) repair via homologous recombination is generally construed as a high-fidelity process. However, some molecular genetic observations show that the recombination and the recombinational DSB repair may be mutagenic and even highly mutagenic. Here we developed an effective and precise method for studying the fidelity of DSB repair in vivo by combining DSBs produced site-specifically by the SegC endonuclease with the famous advantages of the recombination analysis of bacteriophage T4 rII mutants. The method is based on the comparison of the rate of reversion of rII mutation in the presence and in the absence of a DSB repair event initiated in the proximity of the mutation. We observed that DSB repair may moderately (up to 6-fold) increase the apparent reversion frequency, the effect of being dependent on the mutation structure. We also studied the effect of the 14 recombinase deficiency (amber mutation in the uvsX gene) on the fidelity of DSB repair. We observed that DSBs are still repaired via homologous recombination in the uvsX mutants, and the apparent fidelity of this repair is higher than that seen in the wild-type background. The mutator effect of the DSB repair may look unexpected given that most of the normal DNA synthesis in bacteriophage T4 is performed via a recombination-dependent replication (RDR) pathway, which is thought to be indistinguishable from DSB repair. There are three possible explanations for the observed mutagenicity of DSB repair: (1) the origin-dependent (early) DNA replication may be more accurate than the RDR; (2) the step of replication initiation may be more mutagenic than the process of elongation; and (3) the apparent mutagenicity may just reflect some non-randomness in the pool of replicating DNA, i.e., preferential replication of the sequences already involved in replication. We discuss the DSB repair pathway in the absence of UvsX recombinase. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:16 / 23
页数:8
相关论文
共 73 条
[1]   T4 BACTERIOPHAGE GENE-32 - A STRUCTURAL PROTEIN IN REPLICATION AND RECOMBINATION OF DNA [J].
ALBERTS, BM ;
FREY, L .
NATURE, 1970, 227 (5265) :1313-&
[2]   A GENERAL-MODEL FOR THE EVOLUTION OF RECOMBINATION [J].
BARTON, NH .
GENETICAL RESEARCH, 1995, 65 (02) :123-144
[3]   RMPs: Recombination/replication mediator proteins [J].
Beernink, HTH ;
Morrical, SW .
TRENDS IN BIOCHEMICAL SCIENCES, 1999, 24 (10) :385-389
[4]   VARIATIONS IN GENETIC RECOMBINATION DUE TO AMBER MUTATIONS IN T4D BACTERIOPHAGE [J].
BERGER, H ;
WARREN, AJ ;
FRY, KE .
JOURNAL OF VIROLOGY, 1969, 3 (02) :171-&
[5]   Mediator proteins orchestrate enzyme-ssDNA assembly during T4 recombination-dependent DNA replication and repair [J].
Bleuit, JS ;
Xu, H ;
Ma, YJ ;
Wang, TS ;
Liu, J ;
Morrical, SW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (15) :8298-8305
[6]   MOLECULAR AND GENETIC RECOMBINATION OF BACTERIOPHAGE-T4 [J].
BROKER, TR ;
DOERMANN, AH .
ANNUAL REVIEW OF GENETICS, 1975, 9 :213-244
[7]   ACTIVE CISTRON FRAGMENT [J].
CHAMPE, SP ;
BENZER, S .
JOURNAL OF MOLECULAR BIOLOGY, 1962, 4 (03) :288-&
[8]   Tethering on the brink: the evolutionarily conserved Mre11-Rad50 complex [J].
Connelly, JC ;
Leach, DRF .
TRENDS IN BIOCHEMICAL SCIENCES, 2002, 27 (08) :410-418
[9]   Recombination at double-strand breaks and DNA ends: Conserved mechanisms from phage to humans [J].
Cromie, GA ;
Connelly, JC ;
Leach, DRF .
MOLECULAR CELL, 2001, 8 (06) :1163-1174
[10]   MUTATIONS AFFECTING GENETIC-RECOMBINATION IN BACTERIOPHAGE-T4D .1. PATHWAY ANALYSIS [J].
CUNNINGHAM, RP ;
BERGER, H .
VIROLOGY, 1977, 80 (01) :67-82