Pathway maps

DNA damage_ATM/ATR regulation of G1/S checkpoint
DNA damage_ATM/ATR regulation of G1/S checkpoint

Object List (links open in MetaCore):

ATR, I-kB, Cyclin D, Chk2, GADD45 beta, Ubiquitin, Nibrin, USP1, MDM2, GADD45 alpha, BLM, NFBD1, p53, p21, SMC1, Brca1, Claspin, CDC25A, FANCD2, FANCL, Chk1, PCNA, ATRIP, Cyclin E, Cyclin A, ATM, NF-kB, Bard1, CDK4, c-Myc, CDK2, RAD9

Description

ATM/ATR regulation of G1/S and S/G2 checkpoints

DNA damage checkpoints are biochemical pathways that delay or arrest the cell cycle progression in response to the DNA damage. All eukaryotic cells have four phases within the cell cycle, G1, S, G2, and M, and one outside, G0 [1].

The G1/S checkpoint prevents cells from entering the S phase in the presence of the DNA damage by inhibiting the initiation of replication. There are two signal transduction pathways, one to initiate and one to maintain the G1/S arrest [1].

If the DNA damages are double-strand breaks (DSB) caused by ionizing radiation or radiomimetic agents, ataxia telangiectasia mutated serine-protein kinase ( ATM ) is activated [2].

The reaction that initiates the G1/S arrest is phosphorylation of cell cycle checkpoint kinase 2 ( Chk2 ) [1] or cell cycle checkpoint kinase 1 ( Chk1 ) [3] by ATM. Nuclear factor with BRCT domians protein 1 ( NFBD1 ) may participates in transfer signal from ATM to Chk2 [4] and other regulators (e.g. tumor suppressor p53 [5], [6] and breast and ovarian cancer susceptibility protein 1 ( Brca1 ) [7].

Phosphorylated Chk2 in turn inactivates by phosphorylation cell division cycle 25A phosphatase ( Cdc25A ). Lack of active Cdc25A results in the accumulation of the phosphorylated (inactive) form of Cdk2, which is incapable to participate in initiation of replication [1].

14-3-3 proteins participate in regulation activity of some elements G1/S checkpoint pathway (e.g. Chk1 [8], Cdc25A [9] and p53 [10], [11] by controlling the nuclear and cytoplasmic distribution it.

In addition, ATM may regulate oxidative stress-induced signaling cascades involving nuclear factor-kappaB ( NF-KB ), a transcription factor that is upstream of a wide variety of stress-responsive genes. For example, NF-KB activates the transcription of c-Myc [12] (which in turn activates transcription of Cdc25A [13] and tumor suppressor p53 [14].

If the DNA damage is caused by UV light or UV-mimetic agents, the signal leads to phosphorylation of serine/threonine-protein kinase Chk1 by ataxia telangiectasia and Rad3 related protein kinase ( ATR ) with a participation cell cycle checkpoint control rell cycle regulator RAD9 and claspin. The activated Chk1 then phosphorylates Cdc25A, leading to G1 arrest. It is shown, that ATR phosphorylates ATR interacting protein ( ATRIP ), which in turn regulates ATR expression, and is an essential component of the DNA damage checkpoint pathway [15].

Then this rapid response via Chk - Cdc25A pathways is followed by the p53 -mediated maintenance of G1/S arrest. In the maintenance stage, ATM or ATR phosphorylates Ser15 of p53 directly and Ser20 through activation of Chk2 or Chk1 [1]. In addition, the essential elements of p53 regulation are ubiquitination [16] and sumoylation [17].

Phosphorylated p53 activates its target genes, including cyclin-dependent kinase inhibitor 1A ( p21 ), which binds to cyclin-dependent kinase 2 ( Cdk2 ) and cyclin-dependent kinase 4 ( Cdk4 ). It inhibits binding between Cdk and cyclins [1]. Moreover, the DNA damage activates p53 via inhibition its repressor - the ubiquitin-protein ligase E3 MDM2 [18].

The intra-S-phase checkpoint is activated by damage encountered during the S phase or by unrepaired damage that escapes the S/G2 checkpoint and leads to a block in replication. In this pathway ATM phosphorylation of structural maintenance of chromosomes 1-like 1 protein ( SMC1 ) and Fanconi anemia complementation group D2 protein, isoform 1 ( FANCD2 ), with the help of Nibrin, leads to inhibition of replication. It supposed, that phosphorylation of SMC1 results to the repression sister chromatid cohesion [19]. FANCD2 may participate in inhibition of replication via activation Brca1. Brca1 is phosphorylated by ATR (perhaps, with the aid of BML ) or ATM, and activates transcription of growth arrest and DNA-damage-inducible transcripts alpha and beta ( GADD45 alpha/beta ). In addition, the transcription of GADD45 alpha/beta may be regulated by p53. GADD45 alpha/beta was found to bind to proliferating cell nuclear antigen ( PCNA ), a protein involved in DNA replication and repair. p21 blocks the ability of PCNA to bind with Gadd45 [20].

In addition, Chk2/ Cdc25A pathway participates in the S/G2 checkpoint arrest too [21].

References:

  1. Sancar A, Lindsey-Boltz LA, Unsal-Kacmaz K, Linn S
    Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints. Annual review of biochemistry 2004;73:39-85
  2. Bakkenist CJ, Kastan MB
    DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation. Nature 2003 Jan 30;421(6922):499-506
  3. Zhao H, Watkins JL, Piwnica-Worms H
    Disruption of the checkpoint kinase 1/cell division cycle 25A pathway abrogates ionizing radiation-induced S and G2 checkpoints. Proceedings of the National Academy of Sciences of the United States of America 2002 Nov 12;99(23):14795-800
  4. Peng A, Chen PL
    NFBD1, like 53BP1, is an early and redundant transducer mediating Chk2 phosphorylation in response to DNA damage. The Journal of biological chemistry 2003 Mar 14;278(11):8873-6
  5. Xu X, Stern DF
    NFBD1/MDC1 regulates ionizing radiation-induced focus formation by DNA checkpoint signaling and repair factors. The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2003 Oct;17(13):1842-8
  6. Joo WS, Jeffrey PD, Cantor SB, Finnin MS, Livingston DM, Pavletich NP
    Structure of the 53BP1 BRCT region bound to p53 and its comparison to the Brca1 BRCT structure. Genes & development 2002 Mar 1;16(5):583-93
  7. Stucki M, Jackson SP
    MDC1/NFBD1: a key regulator of the DNA damage response in higher eukaryotes. DNA repair 2004 Aug-Sep;3(8-9):953-7
  8. Jiang K, Pereira E, Maxfield M, Russell B, Goudelock DM, Sanchez Y
    Regulation of Chk1 includes chromatin association and 14-3-3 binding following phosphorylation on Ser-345. The Journal of biological chemistry 2003 Jul 4;278(27):25207-17
  9. Conklin DS, Galaktionov K, Beach D
    14-3-3 proteins associate with cdc25 phosphatases. Proceedings of the National Academy of Sciences of the United States of America 1995 Aug 15;92(17):7892-6
  10. Stavridi ES, Chehab NH, Malikzay A, Halazonetis TD
    Substitutions that compromise the ionizing radiation-induced association of p53 with 14-3-3 proteins also compromise the ability of p53 to induce cell cycle arrest. Cancer research 2001 Oct 1;61(19):7030-3
  11. Mhawech P
    14-3-3 proteins--an update. Cell research 2005 Apr;15(4):228-36
  12. Bourgarel-Rey V, Vallee S, Rimet O, Champion S, Braguer D, Desobry A, Briand C, Barra Y
    Involvement of nuclear factor kappaB in c-Myc induction by tubulin polymerization inhibitors. Molecular pharmacology 2001 May;59(5):1165-70
  13. Zornig M, Evan GI
    Cell cycle: on target with Myc. Current biology : CB 1996 Dec 1;6(12):1553-6
  14. Aleyasin H, Cregan SP, Iyirhiaro G, O'Hare MJ, Callaghan SM, Slack RS, Park DS
    Nuclear factor-(kappa)B modulates the p53 response in neurons exposed to DNA damage. The Journal of neuroscience : the official journal of the Society for Neuroscience 2004 Mar 24;24(12):2963-73
  15. Cortez D, Guntuku S, Qin J, Elledge SJ
    ATR and ATRIP: partners in checkpoint signaling. Science 2001 Nov 23;294(5547):1713-6
  16. Oren M, Damalas A, Gottlieb T, Michael D, Taplick J, Leal JF, Maya R, Moas M, Seger R, Taya Y, Ben-Ze'Ev A
    Regulation of p53: intricate loops and delicate balances. Annals of the New York Academy of Sciences 2002 Nov;973:374-83
  17. Melchior F, Hengst L
    SUMO-1 and p53. Cell cycle (Georgetown, Tex.) 2002 Jul-Aug;1(4):245-9
  18. de Toledo SM, Azzam EI, Dahlberg WK, Gooding TB, Little JB
    ATM complexes with HDM2 and promotes its rapid phosphorylation in a p53-independent manner in normal and tumor human cells exposed to ionizing radiation. Oncogene 2000 Dec 14;19(54):6185-93
  19. Kim ST, Xu B, Kastan MB
    Involvement of the cohesin protein, Smc1, in Atm-dependent and independent responses to DNA damage. Genes & development 2002 Mar 1;16(5):560-70
  20. Chen IT, Smith ML, O'Connor PM, Fornace AJ Jr
    Direct interaction of Gadd45 with PCNA and evidence for competitive interaction of Gadd45 and p21Waf1/Cip1 with PCNA. Oncogene 1995 Nov 16;11(10):1931-7
  21. Yazdi PT, Wang Y, Zhao S, Patel N, Lee EY, Qin J
    SMC1 is a downstream effector in the ATM/NBS1 branch of the human S-phase checkpoint. Genes & development 2002 Mar 1;16(5):571-82