Phospho-Ser/Thr-binding domains: navigating the cell cycle and DNA damage response

被引:217
作者
Reinhardt, H. Christian [1 ,2 ,3 ,4 ]
Yaffe, Michael B. [1 ,2 ,5 ]
机构
[1] MIT, Dept Biol, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[2] MIT, Dept Biol Engn, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[3] Univ Hosp Cologne, Ctr Internal Med, Div Hematol & Oncol, D-50937 Cologne, Germany
[4] Cluster Excellence Cellular Stress Responses Agin, Cologne, Germany
[5] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Surg, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
POLO-LIKE KINASE-1; PEPTIDYL-PROLYL ISOMERASE; REPLICATION CHECKPOINT RESPONSE; SCF UBIQUITIN-LIGASE; DOUBLE-STRAND BREAKS; CHK2; PROTEIN-KINASE; S-PHASE CHECKPOINT; F-BOX PROTEINS; STRUCTURAL BASIS; FHA DOMAIN;
D O I
10.1038/nrm3640
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Coordinated progression through the cell cycle is a complex challenge for eukaryotic cells. Following genotoxic stress, diverse molecular signals must be integrated to establish checkpoints specific for each cell cycle stage, allowing time for various types of DNA repair. Phospho-Ser/Thr-binding domains have emerged as crucial regulators of cell cycle progression and DNA damage signalling. Such domains include 14-3-3 proteins, WW domains, Polo-box domains (in PLK1), WD40 repeats (including those in the E3 ligase SCF beta TrCP), BRCT domains (including those in BRCA1) and FHA domains (such as in CHK2 and MDC1). Progress has been made in our understanding of the motif (or motifs) that these phospho-Ser/Thr-binding domains connect with on their targets and how these interactions influence the cell cycle and DNA damage response.
引用
收藏
页码:563 / 580
页数:18
相关论文
共 248 条
  • [81] CDK11p58 is required for the maintenance of sister chromatid cohesion
    Hu, Dongli
    Valentine, Marcus
    Kidd, Vincent J.
    Lahti, Jill M.
    [J]. JOURNAL OF CELL SCIENCE, 2007, 120 (14) : 2424 - 2434
  • [82] RNF8 transduces the DNA-damage signal via histone ubiquitylation and checkpoint protein assembly
    Huen, Michael S. Y.
    Grant, Robert
    Manke, Isaac
    Minn, Kay
    Yu, Xiaochun
    Yaffe, Michael B.
    Chen, Junjie
    [J]. CELL, 2007, 131 (05) : 901 - 914
  • [83] Methylated lysine 79 of histone H3 targets 53BP1 to DNA double-strand breaks
    Huyen, Y
    Zgheib, O
    DiTullio, RA
    Gorgoulis, VG
    Zacharatos, P
    Petty, TJ
    Sheston, EA
    Mellert, HS
    Stavridi, ES
    Halazonetis, TD
    [J]. NATURE, 2004, 432 (7015) : 406 - 411
  • [84] ELIMINATION OF CDC2 PHOSPHORYLATION SITES IN THE CDC25 PHOSPHATASE BLOCKS INITIATION OF M-PHASE
    IZUMI, T
    MALLER, JL
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1993, 4 (12) : 1337 - 1350
  • [85] Phosphorylation of threonine 210 and the role of serine 137 in the regulation of mammalian polo-like kinase
    Jang, YJ
    Ma, S
    Terada, Y
    Erikson, RL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (46) : 44115 - 44120
  • [86] SCFβ-TRCP links Chk1 signaling to degradation of the Cdc25A protein phosphatase
    Jin, JP
    Shirogane, T
    Xu, L
    Nalepa, G
    Qin, J
    Elledge, SJ
    Harper, JW
    [J]. GENES & DEVELOPMENT, 2003, 17 (24) : 3062 - 3074
  • [87] Plk1 activation by Ste20-like kinase (Slk) phosphorylation and polo-box phosphopeptide binding assayed with the substrate translationally controlled tumor protein (TCTP)
    Johnson, Tim M.
    Antrobus, Robin
    Johnson, Louise N.
    [J]. BIOCHEMISTRY, 2008, 47 (12) : 3688 - 3696
  • [88] Structure of the 53BP1 BRCT region bound to p53 and its comparison to the Brcal1 BRCT structure
    Joo, WS
    Jeffrey, PD
    Cantor, SB
    Finnin, MS
    Livingston, DM
    Pavletich, NP
    [J]. GENES & DEVELOPMENT, 2002, 16 (05) : 583 - 593
  • [89] Human PTIP facilitates ATM-mediated activation of p53 and promotes cellular resistance to ionizing radiation
    Jowsey, PA
    Doherty, AJ
    Rouse, J
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (53) : 55562 - 55569
  • [90] Identification of a novel kinesin-related protein, KRMP1, as a target for mitotic peptidyl-prolyl isomerase Pin1
    Kamimoto, T
    Zama, T
    Aoki, R
    Muro, Y
    Hagiwara, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (40) : 37520 - 37528