- DNA-PKcs
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DNA-dependent protein kinase, catalytic subunit, also known as DNA-PKcs, is an enzyme that in humans is encoded by the PRKDC gene.[1] DNA-PKcs belongs to the phosphatidylinositol 3-kinase-related kinase protein family.
Contents
Function
DNA-PKcs is the catalytic subunit of a nuclear DNA-dependent serine/threonine protein kinase called DNA-PK. The second component is the autoimmune antigen Ku. On its own, DNA-PKcs is inactive and relies on Ku to direct it to DNA ends and trigger its kinase activity[2] DNA-PKcs is required for the non-homologous end joining (NHEJ) pathway of DNA repair, which rejoins double-strand breaks. It is also required for V(D)J recombination, a process that utilizes NHEJ to promote immune system diversity. DNA-PKcs knockout mice have severe combined immunodeficiency due to their V(D)J recombination defect.
Many proteins have been identified as substrates for the kinase activity of DNA-PK. Autophosphorylation of DNA-PKcs appears to play a key role in NHEJ and is thought to induce a conformational change that allows end processing enzymes to access the ends of the double-strand break.[3] DNA-PK also cooperates with ATR and ATM to phosphorylate proteins involved in the DNA damage checkpoint.
Interactions
DNA-PKcs has been shown to interact with NCOA6,[4] CHEK1,[5][6] Werner syndrome ATP-dependent helicase,[5][7] RPA2,[8] ILF3,[9] DCLRE1C,[10] ILF2,[9] Ataxia telangiectasia mutated,[5][11] Ku80,[12][13][14] CDC5L,[15] P53,[5][6][16] CIB1,[17] C1D[16] and CHUK.[18]
See also
References
- ^ Sipley JD, Menninger JC, Hartley KO, Ward DC, Jackson SP, Anderson CW (August 1995). "Gene for the catalytic subunit of the human DNA-activated protein kinase maps to the site of the XRCC7 gene on chromosome 8". Proc. Natl. Acad. Sci. U.S.A. 92 (16): 7515–9. doi:10.1073/pnas.92.16.7515. PMC 41370. PMID 7638222. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=41370.
- ^ "Entrez Gene: PRKDC protein kinase, DNA-activated, catalytic polypeptide". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5591.
- ^ Meek K, Dang V, Lees-Miller SP (2008). "DNA-PK: the means to justify the ends?". Adv. Immunol. 99: 33–58. doi:10.1016/S0065-2776(08)00602-0. PMID 19117531.
- ^ Ko, L; Cardona G R, Chin W W (May. 2000). "Thyroid hormone receptor-binding protein, an LXXLL motif-containing protein, functions as a general coactivator". Proc. Natl. Acad. Sci. U.S.A. (UNITED STATES) 97 (11): 6212–7. doi:10.1073/pnas.97.11.6212. ISSN 0027-8424. PMC 18584. PMID 10823961. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=18584.
- ^ a b c d Kim, S T; Lim D S, Canman C E, Kastan M B (Dec. 1999). "Substrate specificities and identification of putative substrates of ATM kinase family members". J. Biol. Chem. (UNITED STATES) 274 (53): 37538–43. doi:10.1074/jbc.274.53.37538. ISSN 0021-9258. PMID 10608806.
- ^ a b Goudelock, Dawn Marie; Jiang Kecheng, Pereira Elizabeth, Russell Beatriz, Sanchez Yolanda (Aug. 2003). "Regulatory interactions between the checkpoint kinase Chk1 and the proteins of the DNA-dependent protein kinase complex". J. Biol. Chem. (United States) 278 (32): 29940–7. doi:10.1074/jbc.M301765200. ISSN 0021-9258. PMID 12756247.
- ^ Karmakar, Parimal; Piotrowski Jason, Brosh Robert M, Sommers Joshua A, Miller Susan P Lees, Cheng Wen-Hsing, Snowden Carey M, Ramsden Dale A, Bohr Vilhelm A (May. 2002). "Werner protein is a target of DNA-dependent protein kinase in vivo and in vitro, and its catalytic activities are regulated by phosphorylation". J. Biol. Chem. (United States) 277 (21): 18291–302. doi:10.1074/jbc.M111523200. ISSN 0021-9258. PMID 11889123.
- ^ Shao, R G; Cao C X, Zhang H, Kohn K W, Wold M S, Pommier Y (Mar. 1999). "Replication-mediated DNA damage by camptothecin induces phosphorylation of RPA by DNA-dependent protein kinase and dissociates RPA:DNA-PK complexes". EMBO J. (ENGLAND) 18 (5): 1397–406. doi:10.1093/emboj/18.5.1397. ISSN 0261-4189. PMC 1171229. PMID 10064605. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1171229.
- ^ a b Ting, N S; Kao P N, Chan D W, Lintott L G, Lees-Miller S P (Jan. 1998). "DNA-dependent protein kinase interacts with antigen receptor response element binding proteins NF90 and NF45". J. Biol. Chem. (UNITED STATES) 273 (4): 2136–45. doi:10.1074/jbc.273.4.2136. ISSN 0021-9258. PMID 9442054.
- ^ Ma, Yunmei; Pannicke Ulrich, Schwarz Klaus, Lieber Michael R (Mar. 2002). "Hairpin opening and overhang processing by an Artemis/DNA-dependent protein kinase complex in nonhomologous end joining and V(D)J recombination". Cell (United States) 108 (6): 781–94. doi:10.1016/S0092-8674(02)00671-2. ISSN 0092-8674. PMID 11955432.
- ^ Suzuki, K; Kodama S, Watanabe M (Sep. 1999). "Recruitment of ATM protein to double strand DNA irradiated with ionizing radiation". J. Biol. Chem. (UNITED STATES) 274 (36): 25571–5. doi:10.1074/jbc.274.36.25571. ISSN 0021-9258. PMID 10464290.
- ^ Jin, S; Kharbanda S, Mayer B, Kufe D, Weaver D T (Oct. 1997). "Binding of Ku and c-Abl at the kinase homology region of DNA-dependent protein kinase catalytic subunit". J. Biol. Chem. (UNITED STATES) 272 (40): 24763–6. doi:10.1074/jbc.272.40.24763. ISSN 0021-9258. PMID 9312071.
- ^ Matheos, Diamanto; Ruiz Marcia T, Price Gerald B, Zannis-Hadjopoulos Maria (Oct. 2002). "Ku antigen, an origin-specific binding protein that associates with replication proteins, is required for mammalian DNA replication". Biochim. Biophys. Acta (Netherlands) 1578 (1-3): 59–72. doi:10.1016/S0167-4781(02)00497-9. ISSN 0006-3002. PMID 12393188.
- ^ Gell, D; Jackson S P (Sep. 1999). "Mapping of protein-protein interactions within the DNA-dependent protein kinase complex". Nucleic Acids Res. (ENGLAND) 27 (17): 3494–502. doi:10.1093/nar/27.17.3494. PMC 148593. PMID 10446239. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=148593.
- ^ Ajuh, P; Kuster B, Panov K, Zomerdijk J C, Mann M, Lamond A I (Dec. 2000). "Functional analysis of the human CDC5L complex and identification of its components by mass spectrometry". EMBO J. (ENGLAND) 19 (23): 6569–81. doi:10.1093/emboj/19.23.6569. ISSN 0261-4189. PMC 305846. PMID 11101529. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=305846.
- ^ a b Yavuzer, U; Smith G C, Bliss T, Werner D, Jackson S P (Jul. 1998). "DNA end-independent activation of DNA-PK mediated via association with the DNA-binding protein C1D". Genes Dev. (UNITED STATES) 12 (14): 2188–99. doi:10.1101/gad.12.14.2188. ISSN 0890-9369. PMC 317006. PMID 9679063. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=317006.
- ^ Wu, X; Lieber M R (Oct. 1997). "Interaction between DNA-dependent protein kinase and a novel protein, KIP". Mutat. Res. (NETHERLANDS) 385 (1): 13–20. ISSN 0027-5107. PMID 9372844.
- ^ Liu, L; Kwak Y T, Bex F, García-Martínez L F, Li X H, Meek K, Lane W S, Gaynor R B (Jul. 1998). "DNA-dependent protein kinase phosphorylation of IkappaB alpha and IkappaB beta regulates NF-kappaB DNA binding properties". Mol. Cell. Biol. (UNITED STATES) 18 (7): 4221–34. ISSN 0270-7306. PMC 109006. PMID 9632806. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=109006.
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