Levels of MCM4 phosphorylation and DNA synthesis in DNA replication block checkpoint control

被引:24
作者
Ishimi, Y
Komamura-Kohno, Y
Karasawa-Shimizu, K
Yamada, K
机构
[1] Mitsubishi Kagaku Inst Life Sci, Tokyo 1948511, Japan
[2] Natl Inst Hlth & Nutr, Shinjuku Ku, Tokyo 1628636, Japan
关键词
MCM proteins; DNA helicase; DNA replication checkpoint; UV irradiation; phosphorylation of MCM4; DNA synthesis; phosphoantibodies;
D O I
10.1016/j.jsb.2003.11.027
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
Blockage of a DNA replication fork movement not only stabilizes the fork structure but also prevents initiation of DNA replication. We reported that MCM4, a subunit of a putative replicative DNA helicase, is extensively phosphorylated in the presence of hydroxyurea (HU) or after exposure to UV irradiation. Here we examined the relationship between levels of MCM4 phosphorylation and DNA synthesis during DNA replication checkpoint control and after release of the control. The results suggest that there is roughly inverse correlation between these two levels; namely the higher the level of MCM4 phosphorylation, the lower the level of DNA synthesis. The presence of HU or UV irradiation can stimulate phosphorylation at several cyclin-dependent kinase (CDK) sites in MCM4, which can lead to inhibition of MCM4/6/7 helicase activity. These results are consistent with the notion that the phosphorylation of MCM4 is involved in regulation of DNA synthesis in the checkpoint control. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:234 / 241
页数:8
相关论文
共 32 条
  • [1] A globular complex formation by Nda1 and the other five members of the MCM protein family in fission yeast
    Adachi, Y
    Usukura, J
    Yanagida, M
    [J]. GENES TO CELLS, 1997, 2 (07) : 467 - 479
  • [2] DNA replication in eukaryotic cells
    Bell, SP
    Dutta, A
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 2002, 71 : 333 - 374
  • [3] DNA replication checkpoint
    Boddy, MN
    Russell, P
    [J]. CURRENT BIOLOGY, 2001, 11 (23) : R953 - R956
  • [4] An ATR- and Cdc7-dependent DNA damage checkpoint that inhibits initiation of DNA replication
    Costanzo, V
    Shechter, D
    Lupardus, PJ
    Cimprich, KA
    Gottesman, M
    Gautier, J
    [J]. MOLECULAR CELL, 2003, 11 (01) : 203 - 213
  • [5] Activation of mammalian Chk1 during DNA replication arrest: a role for Chk1 in the intra-S phase checkpoint monitoring replication origin firing
    Feijoo, C
    Hall-Jackson, C
    Wu, R
    Jenkins, D
    Leitch, J
    Gilbert, DM
    Smythe, C
    [J]. JOURNAL OF CELL BIOLOGY, 2001, 154 (05) : 913 - 923
  • [6] Cell cycle- and chromatin binding state-dependent phosphorylation of human MCM heterohexameric complexes - A role for cdc2 kinase
    Fujita, M
    Yamada, C
    Tsurumi, T
    Hanaoka, F
    Matsuzawa, K
    Inagaki, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (27) : 17095 - 17101
  • [7] Phosphorylation of MCM4 by cdc2 protein kinase inhibits the activity of the minichromosome maintenance complex
    Hendrickson, M
    Madine, M
    Dalton, S
    Gautier, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (22) : 12223 - 12228
  • [8] Inhibition of Mcm4,6,7 helicase activity by phosphorylation with cyclin A/Cdk2
    Ishimi, Y
    Komamura-Kohno, Y
    You, ZY
    Omori, A
    Kitagawa, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (21) : 16235 - 16241
  • [9] Identification of MCM4 as a target of the DNA replication block checkpoint system
    Ishimi, Y
    Komamura-Kohno, Y
    Kwon, HJ
    Yamada, K
    Nakanishi, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (27) : 24644 - 24650
  • [10] A DNA helicase activity is associated with an MCM4, -6, and -7 protein complex
    Ishimi, Y
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (39) : 24508 - 24513