RuvAB-directed branch migration of individual Holliday junctions is impeded by sequence

被引:22
作者
Dennis, C
Fedorov, A
Käs, E
Salomé, L
Grigoriev, M
机构
[1] CNRS, Lab Biol Mol Eucaryote, UMR 5099, Inst Explorat Fonct Genom, F-31062 Toulouse, France
[2] Univ Toulouse 3, F-31062 Toulouse, France
[3] CNRS, Ctr Etud Spatiale Rayonnements, UPR 8002, Toulouse, France
[4] CNRS, UMR 5089, Inst Pharmacol & Biol Struct, Toulouse, France
关键词
hexameric helicase; Holliday junction; homologous recombination; RuvAB; tethered-particle motion;
D O I
10.1038/sj.emboj.7600249
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
The Holliday junction, the key intermediate of recombination, is generated by strand exchange resulting in a covalent connection between two recombining DNA molecules. Translocation of a Holliday junction along DNA, or branch migration, progressively exchanges one DNA strand for another and determines the amount of information that is transferred between two recombining partners. In Escherichia coli, the RuvAB protein complex promotes rapid and unidirectional branch migration of Holliday junctions. We have studied translocation of Holliday junctions using a quantitative biochemical system together with a 'single-molecule' branch migration assay. We demonstrate that RuvAB translocates the junctions through identical DNA sequences in a processive manner with a broad distribution of individual branch migration rates. However, when the complex encounters short heterologous sequences, translocation of the Holliday junctions is impeded. We conclude that translocation of the junctions through a sequence heterology occurs with a probability of bypass being determined both by the length of the heterologous region and the lifetime of the stalled RuvAB complex.
引用
收藏
页码:2413 / 2422
页数:10
相关论文
共 32 条
[1]   Bypass of DNA heterologies during RuvAB-mediated three- and four-strand branch migration [J].
Adams, DE ;
West, SC .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 263 (04) :582-596
[2]   Crystal structure of the Holliday junction DNA in complex with a single RuvA tetramer [J].
Ariyoshi, M ;
Nishino, T ;
Iwasaki, H ;
Shinagawa, H ;
Morikawa, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) :8257-8262
[3]   Processive translocation and DNA unwinding by individual RecBCD enzyme molecules [J].
Bianco, PR ;
Brewer, LR ;
Corzett, M ;
Balhorn, R ;
Yeh, Y ;
Kowalczykowski, SC ;
Baskin, RJ .
NATURE, 2001, 409 (6818) :374-378
[4]   SINGLE-TURNOVER KINETICS OF HELICASE-CATALYZED DNA UNWINDING MONITORED CONTINUOUSLY BY FLUORESCENCE ENERGY-TRANSFER [J].
BJORNSON, KP ;
AMARATUNGA, M ;
MOORE, KJM ;
LOHMAN, TM .
BIOCHEMISTRY, 1994, 33 (47) :14306-14316
[5]   Homologous recombination proteins in prokaryotes and eukaryotes [J].
CameriniOtero, RD ;
Hsieh, P .
ANNUAL REVIEW OF GENETICS, 1995, 29 :509-552
[6]   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
[7]   χ-Sequence recognition and DNA translocation by single RecBCD helicase/nuclease molecules [J].
Dohoney, KM ;
Gelles, J .
NATURE, 2001, 409 (6818) :370-374
[8]   MEASUREMENT OF LACTOSE REPRESSOR-MEDIATED LOOP FORMATION AND BREAKDOWN IN SINGLE DNA-MOLECULES [J].
FINZI, L ;
GELLES, J .
SCIENCE, 1995, 267 (5196) :378-380
[9]   Migration of a holliday junction through a nucleosome directed by the E-coli RuvAB motor protein [J].
Grigoriev, M ;
Hsieh, P .
MOLECULAR CELL, 1998, 2 (03) :373-381
[10]   Crystal structure of E-coli RuvA with bound DNA Holliday junction at 6 Å resolution [J].
Hargreaves, D ;
Rice, DW ;
Sedelnikova, SE ;
Artymiuk, PJ ;
Lloyd, RG ;
Rafferty, JB .
NATURE STRUCTURAL BIOLOGY, 1998, 5 (06) :441-446