DNA replication and homologous recombination factors: acting together to maintain genome stability

被引:36
作者
Aze, Antoine [1 ]
Zhou, Jin Chuan [1 ]
Costa, Alessandro [1 ]
Costanzo, Vincenzo [1 ]
机构
[1] Imperial Canc Res Fund, Clare Hall Labs, London Res Inst, S Mimms EN6 3LD, Herts, England
基金
欧洲研究理事会;
关键词
MINICHROMOSOME MAINTENANCE PROTEIN; BREAK-INDUCED REPLICATION; HUMAN GINS COMPLEX; POLYMERASE-EPSILON; CRYSTAL-STRUCTURE; FUNCTIONAL INSIGHTS; MCM2-7; HELICASE; POL EPSILON; SCHIZOSACCHAROMYCES-POMBE; CATALYTIC DOMAINS;
D O I
10.1007/s00412-013-0411-3
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
Genome duplication requires the coordinated action of multiple proteins to ensure a fast replication with high fidelity. These factors form a complex called the Replisome, which is assembled onto the DNA duplex to promote its unwinding and to catalyze the polymerization of two new strands. Key constituents of the Replisome are the Cdc45-Mcm2-7-GINS helicase and the And1-Claspin-Tipin-Tim1 complex, which coordinate DNA unwinding with polymerase alpha-, delta-, and epsilon- dependent DNA polymerization. These factors encounter numerous obstacles, such as endogenous DNA lesions leading to template breakage and complex structures arising from intrinsic features of specific DNA sequences. To overcome these roadblocks, homologous recombination DNA repair factors, such as Rad51 and the Mre11-Rad50-Nbs1 complex, are required to ensure complete and faithful replication. Consistent with this notion, many of the genes involved in this process result in lethal phenotypes when inactivated in organisms with complex and large genomes. Here, we summarize the architectural and functional properties of the Replisome and propose a unified view of DNA replication and repair processes.
引用
收藏
页码:401 / 413
页数:13
相关论文
共 121 条
[1]   The Histone Chaperone Facilitates Chromatin Transcription (FACT) Protein Maintains Normal Replication Fork Rates [J].
Abe, Takuya ;
Sugimura, Kazuto ;
Hosono, Yoshifumi ;
Takami, Yasunari ;
Akita, Motomu ;
Yoshimura, Akari ;
Tada, Shusuke ;
Nakayama, Tatsuo ;
Murofushi, Hiromu ;
Okumura, Katsuzumi ;
Takeda, Shunichi ;
Horikoshi, Masami ;
Seki, Masayuki ;
Enomoto, Takemi .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (35) :30504-30512
[2]   Mrc1 transduces signals of DNA replication stress to activate Rad53 [J].
Alcasabas, AA ;
Osborn, AJ ;
Bachant, J ;
Hu, FH ;
Werler, PJH ;
Bousset, K ;
Furuya, K ;
Diffley, JFX ;
Carr, AM ;
Elledge, SJ .
NATURE CELL BIOLOGY, 2001, 3 (11) :958-965
[3]   Strength in numbers: preventing rereplication via multiple mechanisms in eukaryotic cells [J].
Arias, Emily E. ;
Walter, Johannes C. .
GENES & DEVELOPMENT, 2007, 21 (05) :497-518
[4]   Structure of Saccharomyces cerevisiae DNA polymerase epsilon by cryo-electron microscopy [J].
Asturias, FJ ;
Cheung, IK ;
Sabouri, N ;
Chilkova, O ;
Wepplo, D ;
Johansson, E .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2006, 13 (01) :35-43
[5]   Crystal structure of a DNA-dependent RNA polymerase (DNA primase) [J].
Augustin, MA ;
Huber, R ;
Kaiser, JT .
NATURE STRUCTURAL BIOLOGY, 2001, 8 (01) :57-61
[6]   X-ray structure of the complex of regulatory subunits of human DNA polymerase δ [J].
Baranovskiy, Andrey G. ;
Babayeva, Nigar D. ;
Liston, Victoria G. ;
Rogozin, Igor B. ;
Koonin, Eugene V. ;
Pavlov, Youri I. ;
Vassylyev, Dmitry G. ;
Tahirov, Tahir H. .
CELL CYCLE, 2008, 7 (19) :3026-3036
[7]   Intersubunit allosteric communication mediated by a conserved loop in the MCM helicase [J].
Barry, Elizabeth R. ;
Lovett, Janet E. ;
Costa, Alessandro ;
Lea, Susan M. ;
Bell, Stephen D. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (04) :1051-1056
[8]   Studies on Human DNA Polymerase ε and GINS Complex and Their Role in DNA Replication [J].
Bermudez, Vladimir P. ;
Farina, Andrea ;
Raghavan, Vineetha ;
Tappin, Inger ;
Hurwitz, Jerard .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (33) :28963-28977
[9]   The Mcm2-7 complex has in vitro helicase activity [J].
Bochman, Matthew L. ;
Schwacha, Anthony .
MOLECULAR CELL, 2008, 31 (02) :287-293
[10]   The Saccharomyces cerevisiae Mcm6/2 and Mcm5/3 ATPase active sites contribute to the function of the putative Mcm2-7 'gate' [J].
Bochman, Matthew L. ;
Schwacha, Anthony .
NUCLEIC ACIDS RESEARCH, 2010, 38 (18) :6078-6088