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
  • [1] Normalization of nomenclature for peptide motifs as ligands of modular protein domains
    Aasland, R
    Abrams, C
    Ampe, C
    Ball, LJ
    Bedford, MT
    Cesareni, G
    Gimona, M
    Hurley, JH
    Jarchau, T
    Lehto, VP
    Lemmon, MA
    Linding, R
    Mayer, BJ
    Nagai, M
    Sudol, M
    Walter, U
    Winder, SJ
    [J]. FEBS LETTERS, 2002, 513 (01) : 141 - 144
  • [2] Phosphorylation of threonine 68 promotes oligomerization and autophosphorylation of the Chk2 protein kinase via the forkhead-associated domain
    Ahn, JY
    Li, XH
    Davis, HL
    Canman, CE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (22) : 19389 - 19395
  • [3] Ahn JY, 2000, CANCER RES, V60, P5934
  • [4] POSTTRANSLATIONALLY MODIFIED 14-3-3-ISOFORMS AND INHIBITION OF PROTEIN-KINASE-C
    AITKEN, A
    HOWELL, S
    JONES, D
    MADRAZO, J
    MARTIN, H
    PATEL, Y
    ROBINSON, K
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 1995, 149 : 41 - 49
  • [5] Functional specificity in 14-3-3 isoform interactions through dimer formation and phosphorylation. Chromosome location of mammalian isoforms and variants.
    Aitken, A
    [J]. PLANT MOLECULAR BIOLOGY, 2002, 50 (06) : 993 - 1010
  • [6] The Drosophila orthologue of xPlkk1 is not essential for Polo activation and is necessary for proper contractile ring formation
    Alves, PS
    Godinho, SA
    Tavares, AA
    [J]. EXPERIMENTAL CELL RESEARCH, 2006, 312 (03) : 308 - 321
  • [7] Kip1 meets SKP2: new links in cell-cycle control
    Amati, B
    Vlach, J
    [J]. NATURE CELL BIOLOGY, 1999, 1 (04) : E91 - E93
  • [8] Polo-like kinases: conservation and divergence in their functions and regulation
    Archambault, Vincent
    Glover, David M.
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (04) : 265 - 275
  • [9] Mitotic Phosphorylation of Cdc25B Ser321 Disrupts 14-3-3 Binding to the High Affinity Ser323 Site
    Astuti, Puji
    Boutros, Rose
    Ducommun, Bernard
    Gabrielli, Brian
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (45) : 34364 - 34370
  • [10] Chk2 kinase - A busy messenger
    Bartek, J
    Falck, J
    Lukas, J
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2001, 2 (12) : 877 - 886