SQ/TQ cluster domains: concentrated ATM/ATR kinase phosphorylation site regions in DNA-damage-response proteins

被引:171
作者
Traven, A
Heierhorst, J
机构
[1] St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia
[2] Univ Melbourne, Dept Med, Fitzroy, Vic 3065, Australia
关键词
D O I
10.1002/bies.20204
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
ATM/ATR-like protein kinases play central roles in the maintenance of genome stability and phosphorylate numerous substrates in response to DNA damage, preferentially on SO or TO motifs. ATM/ATR substrates often contain several closely spaced SQ/TQ motifs in regions that have been termed SQ/TQ cluster domains (SCDs). SCDs are now considered a structural hallmark of DNA-damage-response proteins. Mutational analyses of a number of SCD-containing proteins indicate that multisite phosphorylation of SQ/TQ motifs is required for normal DNA-damage responses, most commonly by mediating protein-protein interactions in the formation of DNA-damage-induced complexes. SCD sequences are highly diverse and these domains may be largely unfolded in their native state rather than adopting a common three-dimensional fold. Structural disorder of SCDs could be advantageous for efficient phosphorylation by ATM/ATR kinases and also enable them to be molded into distinct conformations to facilitate flexible interactions with multiple binding partners. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:397 / 407
页数:11
相关论文
共 94 条
  • [1] Cell cycle checkpoint signaling through the ATM and ATR kinases
    Abraham, RT
    [J]. GENES & DEVELOPMENT, 2001, 15 (17) : 2177 - 2196
  • [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] 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
  • [4] Phosphorylation and rapid relocalization of 53BP1 to nuclear foci upon DNA damage
    Anderson, L
    Henderson, C
    Adachi, Y
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (05) : 1719 - 1729
  • [5] ATR couples FANCD2 monoubiquitination to the DNA-damage response
    Andreassen, PR
    D'Andrea, AD
    Taniguchi, T
    [J]. GENES & DEVELOPMENT, 2004, 18 (16) : 1958 - 1963
  • [6] DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation
    Bakkenist, CJ
    Kastan, MB
    [J]. NATURE, 2003, 421 (6922) : 499 - 506
  • [7] ATR/ATM-mediated phosphorylation of human Rad17 is required for genotoxic stress responses
    Bao, SD
    Tibbetts, RS
    Brumbaugh, KM
    Fang, YN
    Richardson, DA
    Ali, A
    Chen, SM
    Abraham, RT
    Wang, XF
    [J]. NATURE, 2001, 411 (6840) : 969 - 974
  • [8] Direct kinase-to-kinase signaling mediated by the FHA phosphoprotein recognition domain of the Dun1 DNA damage checkpoint kinase
    Bashkirov, VI
    Bashkirova, EV
    Haghnazari, E
    Heyer, WD
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (04) : 1441 - 1452
  • [9] Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome
    Bell, DW
    Varley, JM
    Szydlo, TE
    Kang, DH
    Wahrer, DCR
    Shannon, KE
    Lubratovich, M
    Verselis, SJ
    Isselbacher, KJ
    Fraumeni, JF
    Birch, JM
    Li, FP
    Garber, JE
    Haber, DA
    [J]. SCIENCE, 1999, 286 (5449) : 2528 - 2531
  • [10] DNA damage-induced translocation of the Werner helicase is regulated by acetylation
    Blander, G
    Zalle, N
    Daniely, Y
    Taplick, J
    Gray, MD
    Oren, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (52) : 50934 - 50940