Active DNA unwinding dynamics during processive DNA replication

被引:61
作者
Morin, Jose A. [2 ,3 ]
Cao, Francisco J. [4 ]
Lazaro, Jose M. [1 ]
Ricardo Arias-Gonzalez, J. [2 ,5 ]
Valpuesta, Jose M. [5 ]
Carrascosa, Jose L. [2 ,5 ]
Salas, Margarita [1 ]
Ibarra, Borja [2 ,5 ]
机构
[1] Univ Autonoma Madrid, Ctr Biol Mol Severo Ochoa, Consejo Super Invest Cient, E-28049 Madrid, Spain
[2] Inst Madrileno Estudios Avanzados, Madrid 28049, Spain
[3] Ctr Estudios Avanzados Cuba, Havana 17100, Cuba
[4] Univ Complutense, Dept Fis Atom Mol & Nucl, E-28040 Madrid, Spain
[5] Consejo Super Invest Cient, Ctr Nacl Biotecnol, Dept Estruct Macromol, Madrid 28049, Spain
关键词
molecular motors; single-molecule; strand displacement; replicative DNA polymerase; STRAND-DISPLACEMENT; BACTERIOPHAGE PHI-29; HEXAMERIC HELICASE; FINGERS SUBDOMAIN; CRYSTAL-STRUCTURE; SINGLE-MOLECULE; POLYMERASE; MECHANISM; FORCE; TRANSLOCATION;
D O I
10.1073/pnas.1204759109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Duplication of double-stranded DNA (dsDNA) requires a fine-tuned coordination between the DNA replication and unwinding reactions. Using optical tweezers, we probed the coupling dynamics between these two activities when they are simultaneously carried out by individual Phi29 DNA polymerase molecules replicating a dsDNA hairpin. We used the wild-type and an unwinding deficient polymerase variant and found that mechanical tension applied on the DNA and the DNA sequence modulate in different ways the replication, unwinding rates, and pause kinetics of each polymerase. However, incorporation of pause kinetics in a model to quantify the unwinding reaction reveals that both polymerases destabilize the fork with the same active mechanism and offers insights into the topological strategies that could be used by the Phi29 DNA polymerase and other DNA replication systems to couple unwinding and replication reactions.
引用
收藏
页码:8115 / 8120
页数:6
相关论文
共 39 条
[1]   Asymmetric interactions of hexameric bacteriophage T7 DNA helicase with the 5′- and 3′-tails of the forked DNA substrate [J].
Ahnert, P ;
Patel, SS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (51) :32267-32273
[2]   Structures of phi29 DNA polymerase complexed with substrate:: The mechanism of translocation in B-family polymerases [J].
Berman, Andrea J. ;
Kamtekar, Satwik ;
Goodman, Jessica L. ;
Lazaro, José M. ;
de Vega, Miguel ;
Blanco, Luis ;
Salas, Margarita ;
Steitz, Thomas A. .
EMBO JOURNAL, 2007, 26 (14) :3494-3505
[3]   Opening of nucleic-acid double strands by helicases:: Active versus passive opening -: art. no. 011904 [J].
Betterton, MD ;
Jülicher, F .
PHYSICAL REVIEW E, 2005, 71 (01)
[4]  
BLANCO L, 1989, J BIOL CHEM, V264, P8935
[5]   Mechanical processes in biochemistry [J].
Bustamante, C ;
Chemla, YR ;
Forde, NR ;
Izhaky, D .
ANNUAL REVIEW OF BIOCHEMISTRY, 2004, 73 :705-748
[6]   Replication slippage of different DNA polymerases is inversely related to their strand displacement efficiency [J].
Canceill, D ;
Viguera, E ;
Ehrlich, SD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (39) :27481-27490
[7]   NS3 helicase actively separates RNA strands and senses sequence barriers ahead of the opening fork [J].
Cheng, Wei ;
Dumont, Sophie ;
Tinoco, Ignacio, Jr. ;
Bustamante, Carlos .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (35) :13954-13959
[8]   Nucleic acid unwinding by hepatitis C virus and bacteriophage T7 helicases is sensitive to base pair stability [J].
Donmez, Ilker ;
Rajagopal, Vaishnavi ;
Jeong, Yong-Joo ;
Patel, Smita S. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (29) :21116-21123
[9]   Crystal structure of a bacteriophage T7 DNA replication complex at 2.2 Å resolution [J].
Doublié, S ;
Tabor, S ;
Long, AM ;
Richardson, CC ;
Ellenberger, T .
NATURE, 1998, 391 (6664) :251-258
[10]   Mechanism of DNA translocation in a replicative hexameric helicase [J].
Enemark, Eric J. ;
Joshua-Tor, Leemor .
NATURE, 2006, 442 (7100) :270-275