The S-cerevisiae Rrm3p DNA helicase moves with the replication fork and affects replication of all yeast chromosomes

被引:136
作者
Azvolinsky, Anna [1 ]
Dunaway, Stephen [1 ]
Torres, Jorge Z. [1 ]
Bessler, Jessica B. [1 ]
Zakian, Virginia A. [1 ]
机构
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
关键词
Rrm3p; Mrc1p; DNA replication; helicase; yeast; chromatin;
D O I
10.1101/gad.1478906
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Saccharomyces cerevisiae DNA helicase Rrm3p is needed for normal fork progression through > 1000 discrete sites scattered throughout the genome. Here we show that replication of all yeast chromosomes was markedly delayed in rrm3 cells. Delayed replication was seen even in a region that lacks any predicted Rrm3p-dependent sites. Based on the pattern of replication intermediates in two-dimensional gels, the rate of fork movement in rrm3 cells appeared similar to wild-type except at known Rrm3p-dependent sites. These data suggest that although Rrm3p has a global role in DNA replication, its activity is needed only or primarily at specific, difficult-to-replicate sites. By the criterion of chromatin immunoprecipitation, Rrm3p was associated with both Rrm3p-dependent and -independent sites, and moved with the replication fork through both. In addition, Rrm3p interacted with Pol2p, the catalytic subunit of DNA polymerase epsilon, in vivo. Thus, rather than being recruited to its sites of action when replication forks stall at these sites, Rrm3p is likely a component of the replication fork apparatus.
引用
收藏
页码:3104 / 3116
页数:13
相关论文
共 42 条
  • [1] Cycles of chromosome instability are associated with a fragile site and are increased by defects in DNA replication and checkpoint controls in yeast
    Admire, A
    Shanks, L
    Danzl, N
    Wang, M
    Weier, U
    Stevens, W
    Hunt, E
    Weinert, T
    [J]. GENES & DEVELOPMENT, 2006, 20 (02) : 159 - 173
  • [2] 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
  • [3] 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
  • [5] PROPERTIES OF THE BACTERIOPHAGE-T4 DNA-REPLICATION APPARATUS - THE T4 DDA DNA HELICASE IS REQUIRED TO PASS A BOUND RNA-POLYMERASE MOLECULE
    BEDINGER, P
    HOCHSTRASSER, M
    JONGENEEL, CV
    ALBERTS, BM
    [J]. CELL, 1983, 34 (01) : 115 - 123
  • [6] Roles of Pif1-like helicases in the maintenance of genomic stability
    Boule, Jean-Baptiste
    Zakian, Virginia A.
    [J]. NUCLEIC ACIDS RESEARCH, 2006, 34 (15) : 4147 - 4153
  • [7] 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
  • [8] Helicase structure and mechanism
    Caruthers, JM
    McKay, DB
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 2002, 12 (01) : 123 - 133
  • [9] ATR homolog Mec1 promotes fork progression, thus averting breaks in replication slow zones
    Cha, RS
    Kleckner, N
    [J]. SCIENCE, 2002, 297 (5581) : 602 - 606
  • [10] Helicase-catalysed translocation and strand separation
    Eoff, RL
    Raney, KD
    [J]. BIOCHEMICAL SOCIETY TRANSACTIONS, 2005, 33 : 1474 - 1478