Replication in hydroxyurea: It's a matter of time

被引:176
作者
Alvino, Gina M.
Collingwood, David
Murphy, John M.
Delrow, Jeffrey
Brewer, Bonita J.
Raghuraman, M. K. [1 ]
机构
[1] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
[2] Univ Washington, Dept Math, Seattle, WA 98195 USA
[3] Fred Hutchinson Canc Res Ctr, Dept Genom Resources, Seattle, WA 98109 USA
关键词
D O I
10.1128/MCB.00719-07
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
Hydroxyurea (HU) is a DNA replication inhibitor that negatively affects both the elongation and initiation phases of replication and triggers the "intra-S phase checkpoint." Previous work with budding yeast has shown that, during a short exposure to HU, MEC1/RAD53 prevent initiation at some late S phase origins. In this study, we have performed microarray experiments to follow the fate of all origins over an extended exposure to HU. We show that the genome-wide progression of DNA synthesis, including origin activation, follows the same pattern in the presence of HU as in its absence, although the time frames are very different. We find no evidence for a specific effect that excludes initiation from late origins. Rather, HU causes S phase to proceed in slow motion; all temporal classes of origins are affected, but the order in which they become active is maintained. We propose a revised model for the checkpoint response to HU that accounts for the continued but slowed pace of the temporal program of origin activation.
引用
收藏
页码:6396 / 6406
页数:11
相关论文
共 41 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] THE SAD1/RAD53 PROTEIN-KINASE CONTROLS MULTIPLE CHECKPOINTS AND DNA DAMAGE-INDUCED TRANSCRIPTION IN YEAST
    ALLEN, JB
    ZHOU, Z
    SIEDE, W
    FRIEDBERG, EC
    ELLEDGE, SJ
    [J]. GENES & DEVELOPMENT, 1994, 8 (20) : 2401 - 2415
  • [3] Differential assembly of Cdc45p and DNA polymerases at early and late origins of DNA replication
    Aparicio, OM
    Stout, AM
    Bell, SP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (16) : 9130 - 9135
  • [4] 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] The Cdc7 protein kinase is required for origin firing during S phase
    Bousset, K
    Diffley, JFX
    [J]. GENES & DEVELOPMENT, 1998, 12 (04) : 480 - 490
  • [6] The ATM homologue MEC1 is required for phosphorylation of replication protein A in yeast
    Brush, GS
    Morrow, DM
    Hieter, P
    Kelly, TJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (26) : 15075 - 15080
  • [7] Survival of DNA damage in yeast directly depends on increased dNTP levels allowed by relaxed feedback inhibition of ribonucleotide reductase
    Chabes, A
    Georgieva, B
    Domkin, V
    Zhao, XL
    Rothstein, R
    Thelander, L
    [J]. CELL, 2003, 112 (03) : 391 - 401
  • [8] Yeast Sml1, a protein inhibitor of ribonucleotide reductase
    Chabes, A
    Domkin, V
    Thelander, L
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (51) : 36679 - 36683
  • [9] Recovery from DNA replicational stress is the essential function of the S-phase checkpoint pathway
    Desany, BA
    Alcasabas, AA
    Bachant, JB
    Elledge, SJ
    [J]. GENES & DEVELOPMENT, 1998, 12 (18) : 2956 - 2970
  • [10] Cdc7 is required throughout the yeast S phase to activate replication origins
    Donaldson, AD
    Fangman, WL
    Brewer, BJ
    [J]. GENES & DEVELOPMENT, 1998, 12 (04) : 491 - 501