DNA Damage

Ataxia telangiectasia mutated kinase (ATM) and ataxia telangiectasia and Rad3-related kinase (ATR) are PI3 Kinase-related kinase (PIKK) family members that phosphorylate multiple substrates on serine or threonine residues that are followed by a glutamine in response to DNA damage or replication blocks (1-3). p53 is phosphorylated by ATM, ATR and DNA-PK at Ser15. This phosphorylation impairs the ability of MDM2 to bind p53, promoting both the accumulation and activation of p53 in response to DNA damage (4,5). Chk1 and Chk2, downstream protein kinases of ATM/ATR, plays an important role in DNA damage checkpoint control, embryonic development and tumor suppression (6). Chk1 is phosphorylated at Ser280 and Ser296 following DNA damage. The amino-terminal domain of Chk2 contains a series of seven serine or threonine residues, including Thr68, each followed by glutamine (SQ or TQ motif). After DNA damage by ionizing radiation (IR), UV irradiation or hydroxyurea treatment, Thr68 and other sites in this region become phosphorylated by ATM/ATR (7-9). The breast cancer susceptibility proteins BRCA1 and BRCA2 are frequently mutated in cases of hereditary breast and ovarian cancers and have roles in multiple processes related to DNA damage, repair, cell cycle progression, transcription, ubiquitination and apoptosis. Numerous DNA-damage induced phosphorylation sites on BRCA1 have been identified, including serine 1524, and kinases activated in a cell cycle-dependent manner, including Aurora A and CDK2, can also phosphorylate BRCA1. IR, DNA and radiometric-induced DNA damage also results in rapid phosphorylation of the histone H2A.X family member H2A.X at Ser139 by ATM (10,11). Within minutes following DNA damage, Ser139-phosphorylated H2A.X localizes to sites of DNA damage at subnuclear foci (12).

DNA damage repair pathways

DNA damage repair pathways. Base excision repair (BER), single strand break repair (SSBR), nucleotide excision repair (NER), mismatch repair (MMR), homologous recombination repair (HRR), non-homologous end joining (NHEJ), translesion synthesis (TLS), fanconi anemia (FA), and methylguanine methyltransferase (MGMT) are shown.

Relevant Antibodies

Catalog#Product NameApplicationReactivity
APRab04285ATR (phospho Ser428) Rabbit Polyclonal AntibodyIHC-P,IF-P,IF-F,ICC/IF,ELISAHuman,Rat,Mouse
APRab04332BRCA1 (phospho Ser1524) Rabbit Polyclonal AntibodyWB,IHC-P,IF-P,IF-F,ICC/IF,ELISAHuman,Rat,Mouse
AMRe21000Chk2 (Phospho Thr68) Rabbit Monoclonal antibodyWB,IF,IP,ELISAHuman,Mouse,Rat
APRab04456Chk1 (phospho Ser345) Rabbit Polyclonal AntibodyIHC-P,IF-P,IF-F,ICC/IF,ELISAHuman,Mouse,Rat
AMRe21478Histone H2A.X (Phospho Ser139) Rabbit Monoclonal antibodyWB,IHC,IF,IP,ELISAHuman,Mouse,Rat
APRab00821Phospho-p53 (Ser15) Rabbit Polyclonal AntibodyWB,IHC-F,IHC-P,ICC/IF,IP,ELISAHuman,Rat
AMRe05856Phospho-ATM (S1981) (3F17) Rabbit Monoclonal AntibodyWB,IHC-P,FC,IP,IF-PHuman
APS0635HRP-conjugated Polyclonal Goat Anti-Rabbit IgG(H+L) Secondary AntibodyELISA,WB,DotblotMouse
AMRe80004GAPDH (12R9) Rabbit Monoclonal AntibodyWB,ELISAHuman,Mouse,Rat,Rabbit,Dog,Monkey

Related Products

References

  • Kastan, M.B. and Lim, D.S. (2000) Nat. Rev. Mol. Cell Biol. 1, 179-186.
  • Abraham, R.T. DNA Repair (Amst) 3, 883-887.
  • Shechter, D. et al. DNA Repair (Amst) 3, 901-908.
  • Shieh, S.Y. et al. (1997) Cell 91, 325-334.
  • Tibbetts, R.S. et al. (1999) Genes Dev. 13, 152-157.
  • Martinho, R.G. et al. (1998) EMBO J. 17, 7239-17249.
  • Matsuoka, S. et al. (2000) Proc. Natl. Acad. Sci. USA 97, 10389-10394.
  • Melchionna, R. et al. (2000) Nat. Cell Biol. 2, 762-765.
  • Ahn, J.Y. et al. (2000) Cancer Res. 60, 5934-5936.
  • Rogakou, E.P. et al. (1998) J. Biol. Chem. 273, 5858-5868.
  • Burma, S. et al. (2001) J. Biol. Chem. 276, 42462-42467.
  • Rogakou, E.P. et al. (1999) J. Cell Biol. 146, 905-916.
Voisey

Voisey 

Voisey is a technical support specialist at EnkiLife, proficient in immunology and cell biology. She is committed to providing customers with professional and efficient technical support. Additionally, she is involved in research on customers' fields of study and designs highly cost-effective solutions for them.

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