Mcm8 and Mcm9 Form a Complex that Functions in Homologous Recombination Repair Induced by DNA Interstrand Cross links

被引:108
作者
Nishimura, Kohei [1 ]
Ishiai, Masamichi [2 ]
Horikawa, Kazuki [1 ,3 ]
Fukagawa, Tatsuo [3 ,4 ]
Takata, Minoru [2 ]
Takisawa, Haruhiko [5 ]
Kanemaki, Masato T. [1 ,3 ]
机构
[1] Res Org Informat & Syst, Natl Inst Genet, Frontier Res Ctr, Mishima, Shizuoka 4118540, Japan
[2] Kyoto Univ, Ctr Radiat Biol, Dept Late Effects Studies, Sakyo Ku, Kyoto 6068501, Japan
[3] SOKENDAI, Dept Genet, Mishima, Shizuoka 4118540, Japan
[4] Natl Inst Genet, Div Mol Genet, Mishima, Shizuoka 4118540, Japan
[5] Osaka Univ, Grad Sch Sci, Dept Biol Sci, Toyonaka, Osaka 5600043, Japan
关键词
FANCONI-ANEMIA PATHWAY; DOUBLE-STRAND BREAKS; PROTEIN FAMILY; THERMOCOCCUS KODAKARENSIS; GENOMIC STABILITY; TUMOR SUPPRESSION; CELL-CYCLE; S-PHASE; PROMOTES; REPLICATION;
D O I
10.1016/j.molcel.2012.05.047
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
DNA interstrand crosslinks (ICLs) are highly toxic lesions that stall the replication fork to initiate the repair process during the S phase of vertebrates. Proteins involved in Fanconi anemia (FA), nucleotide excision repair (NER), and translesion synthesis (TS) collaboratively lead to homologous recombination (HR) repair. However, it is not understood how ICL-induced HR repair is carried out and completed. Here, we showed that the replicative helicase-related Mm family of proteins, Mcm8 and Mcm9, forms a complex required for HR repair induced by ICLs. Chicken DT40 cells lacking MCM8 or MCM9 are viable but highly sensitive to ICL-inducing agents, and exhibit more chromosome aberrations in the presence of mitomycin C compared with wild-type cells. During ICL repair, Mcm8 and Mcm9 form nuclear foci that partly colocalize with Rad51. Mcm8-9 works downstream of the FA and BRCA2/Rad51 pathways, and is required for HR that promotes sister chromatid exchanges, probably as a hexameric ATPase/helicase.
引用
收藏
页码:511 / 522
页数:12
相关论文
共 50 条
[21]   Mammalian XRCC2 promotes the repair of DNA double-strand breaks by homologous recombination [J].
Johnson, RD ;
Liu, N ;
Jasin, M .
NATURE, 1999, 401 (6751) :397-399
[22]   Stalled Fork Rescue via Dormant Replication Origins in Unchallenged S Phase Promotes Proper Chromosome Segregation and Tumor Suppression [J].
Kawabata, Tsuyoshi ;
Luebben, Spencer W. ;
Yamaguchi, Satoru ;
Ilves, Ivar ;
Matise, Ilze ;
Buske, Tavanna ;
Botchan, Michael P. ;
Shima, Naoko .
MOLECULAR CELL, 2011, 41 (05) :543-553
[23]   Expanded roles of the Fanconi anemia pathway in preserving genomic stability [J].
Kee, Younghoon ;
D'Andrea, Alan D. .
GENES & DEVELOPMENT, 2010, 24 (16) :1680-1694
[24]   Functional interplay between BRCA2/FancD1 and FancC in DNA repair [J].
Kitao, Hiroyuki ;
Yamamoto, Kazuhiko ;
Matsushita, Nobuko ;
Ohzeki, Mioko ;
Ishiai, Masamichi ;
Takata, Minoru .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (30) :21312-21320
[25]   XRCC2 and XRCC3, new human Rad51-family members, promote chromosome stability and protect against DNA cross-links and other damages [J].
Liu, N ;
Lamerdin, JE ;
Tebbs, RS ;
Schild, D ;
Tucker, JD ;
Shen, MR ;
Brookman, KW ;
Siciliano, MJ ;
Walter, CA ;
Fan, WF ;
Narayana, LS ;
Zhou, ZQ ;
Adamson, AW ;
Sorensen, KJ ;
Chen, DJ ;
Jones, NJ ;
Thompson, LH .
MOLECULAR CELL, 1998, 1 (06) :783-793
[26]   Ancient diversification of eukaryotic MCM DNA replication proteins [J].
Liu, Yuan ;
Richards, Thomas A. ;
Aves, Stephen J. .
BMC EVOLUTIONARY BIOLOGY, 2009, 9
[27]   Mechanism of RAD51-Dependent DNA Interstrand Cross-Link Repair [J].
Long, David T. ;
Raeschle, Markus ;
Joukov, Vladimir ;
Walter, Johannes C. .
SCIENCE, 2011, 333 (6038) :84-87
[28]   Identification of full genes and proteins of MCM9, a novel, vertebrate-specific member of the MCM2-8 protein family [J].
Lutzmann, M ;
Maiorano, D ;
Méchali, M .
GENE, 2005, 362 :51-56
[29]   MCM9 binds Cdt1 and is required for the assembly of prereplication complexes [J].
Lutzmann, Malik ;
Mechali, Marcel .
MOLECULAR CELL, 2008, 31 (02) :190-200
[30]   MCM8 is an MCM2-7-related protein that functions as a DNA helicase during replication elongation and not initiation [J].
Maiorano, D ;
Cuvier, O ;
Danis, E ;
Méchali, M .
CELL, 2005, 120 (03) :315-328