Csm3, Tof1, and Mrc1 Form a Heterotrimeric Mediator Complex That Associates with DNA Replication Forks

被引:110
作者
Bando, Masashige [1 ]
Katou, Yuki [1 ]
Komata, Makiko [1 ]
Tanaka, Hirokazu [1 ]
Itoh, Takehiko [1 ]
Sutani, Takashi [1 ]
Shirahige, Katsuhiko [1 ]
机构
[1] Tokyo Inst Technol, Dept Biol Sci, Lab Chromosome Struct & Funct, Grad Sch Biosci & Biotechnol,Midori Ku, Yokohama, Kanagawa 2268501, Japan
关键词
S-PHASE CHECKPOINT; SACCHAROMYCES-CEREVISIAE; EUKARYOTIC DNA; PROGRESSION; HELICASE; STRESS; RAD53; MCM; COMPONENTS; RESPONSES;
D O I
10.1074/jbc.M109.065730
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
Mrc1(mediator of replication checkpoint), Tof1 (topoisomerase I interacting factor), and Csm3 (chromosome segregation in meiosis) are checkpoint-mediator proteins that function during DNA replication and activate the effector kinase Rad53. We reported previously that Mrc1 and Tof1 are constituents of the replication machinery and that both proteins are required for the proper arrest and stabilization of replication forks in the presence of hydroxyurea. In our current study, we show that Csm3 is a component of moving replication forks and that both Tof1 and Csm3 are specifically required for the association of Mrc1 with these structures. In contrast, the deletion of mrc1 did not affect the association of Tof1 and Csm3 with the replication fork complex. In agreement with previous observations in yeast cells, the results of a baculovirus coexpression system showed that these three proteins interact directly with each other to form a mediator complex in the absence of replication forks.
引用
收藏
页码:34355 / 34365
页数:11
相关论文
共 30 条
  • [1] Mrc1 transduces signals of DNA replication stress to activate Rad53
    Alcasabas, AA
    Osborn, AJ
    Bachant, J
    Hu, FH
    Werler, PJH
    Bousset, K
    Furuya, K
    Diffley, JFX
    Carr, AM
    Elledge, SJ
    [J]. NATURE CELL BIOLOGY, 2001, 3 (11) : 958 - 965
  • [2] Components and dynamics of DNA replication complexes in S-cerevisiae: Redistribution of MCM proteins and Cdc45p during S phase
    Aparicio, OM
    Weinstein, DM
    Bell, SP
    [J]. CELL, 1997, 91 (01) : 59 - 69
  • [3] The DNA damage response during DNA replication
    Branzei, D
    Foiani, M
    [J]. CURRENT OPINION IN CELL BIOLOGY, 2005, 17 (06) : 568 - 575
  • [4] The Rad53 signal transduction pathway: Replication fork stabilization, DNA repair, and adaptation
    Branzei, Dana
    Foiani, Marco
    [J]. EXPERIMENTAL CELL RESEARCH, 2006, 312 (14) : 2654 - 2659
  • [5] Molecular anatomy and regulation of a stable replisome eukaryotic DNA at a paused replication fork
    Calzada, A
    Hodgson, B
    Kanemaki, M
    Bueno, A
    Labib, K
    [J]. GENES & DEVELOPMENT, 2005, 19 (16) : 1905 - 1919
  • [6] A novel multi-purpose cassette for repeated integrative epitope tagging of genes in Saccharomyces cerevisiae
    De Antoni, A
    Gallwitz, D
    [J]. GENE, 2000, 246 (1-2) : 179 - 185
  • [7] Foss EJ, 2001, GENETICS, V157, P567
  • [8] GINS maintains association of Cdc45 with MCM in replisome progression complexes at eukaryotic DNA replication forks
    Gambus, A
    Jones, RC
    Sanchez-Diaz, A
    Kanemaki, M
    van Deursen, F
    Edmondson, RD
    Labib, K
    [J]. NATURE CELL BIOLOGY, 2006, 8 (04) : 358 - U41
  • [9] The S phase checkpoint: When the crowd meets at the fork
    Gottifredi, V
    Prives, C
    [J]. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2005, 16 (03) : 355 - 368
  • [10] Mrc1 and Tof1 regulate DNA replication forks in different ways during normal S Phase
    Hodgson, Ben
    Calzada, Arturo
    Labib, Karim
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2007, 18 (10) : 3894 - 3902