TP53BP1
| |
| Identificadores | |
| Símbolo | TP53BP1 |
| Símbolos alt. | 53BP1, p202, p53BP1, TP53, TDRD30, tumor protein p53 binding protein 1 |
| Entrez | 7158 |
| RefSeq | NP_001135451 |
| UniProt | Q12888 |
| Outros datos | |
| Locus | Cr. 15 15q15.3(43.4 – 43.51 Mb) |
A TP53BP1 ou proteína 1 que se une a p53 supresora de tumores (en inglés tumor suppressor p53-binding protein 1) tamén chamada proteína 1 que se une a p53 ou 53BP1 é unha proteína que nos humanos está codificada no xene TP53BP1 do cromosoma 15.[1][2][3]
Importancia clínica editar
A 53BP1 está subexpresada na maioría dos casos de cancro de mama triplo negativo.[4]
Reparación do ADN editar
As roturas do ADN de dobre febra (DSB) son danos citotóxicos que poden ser reparados ou ben por reparación pola vía da recombinación homóloga (HR) ou ben pola vía de unión de extremos non homólogos (NHEJ). A unión de extremos non homólogos, aínda que é máis rápida que a vía da recombinación homóloga, é menos exacta. O paso diverxente inicial entre as dúas vías é a resección dos extremos, e este paso é regulado por numerosos factores. En particular, BRCA1 e 53BP1 xogan un papel na determinación do balance entre as dúas vías.[5][6] A 53BP1 restrinxe a resección e promove a unión de extremos non homólogos.
Interaccións editar
A 53BP1 interacciona fisicamente con:
Notas editar
- ↑ Iwabuchi K, Bartel PL, Li B, Marraccino R, Fields S (Jun 1994). "Two cellular proteins that bind to wild-type but not mutant p53". Proceedings of the National Academy of Sciences of the United States of America 91 (13): 6098–102. PMC 44145. PMID 8016121. doi:10.1073/pnas.91.13.6098.
- ↑ Iwabuchi K, Li B, Massa HF, Trask BJ, Date T, Fields S (Oct 1998). "Stimulation of p53-mediated transcriptional activation by the p53-binding proteins, 53BP1 and 53BP2". The Journal of Biological Chemistry 273 (40): 26061–8. PMID 9748285. doi:10.1074/jbc.273.40.26061.
- ↑ "Entrez Gene: TP53BP1 tumor protein p53 binding protein 1".
- ↑ Bouwman P, Aly A, Escandell JM, Pieterse M, Bartkova J, van der Gulden H, Hiddingh S, Thanasoula M, Kulkarni A, Yang Q, Haffty BG, Tommiska J, Blomqvist C, Drapkin R, Adams DJ, Nevanlinna H, Bartek J, Tarsounas M, Ganesan S, Jonkers J (Jun 2010). "53BP1 loss rescues BRCA1 deficiency and is associated with triple-negative and BRCA-mutated breast cancers". Nature Structural & Molecular Biology 17 (6): 688–95. PMC 2912507. PMID 20453858. doi:10.1038/nsmb.1831.
- ↑ Panier S, Boulton SJ (2014). "Double-strand break repair: 53BP1 comes into focus". Nat. Rev. Mol. Cell Biol. 15 (1): 7–18. PMID 24326623. doi:10.1038/nrm3719.
- ↑ Li J, Xu X (2016). "DNA double-strand break repair: a tale of pathway choices". Acta Biochim. Biophys. Sin. (Shanghai) 48 (7): 641–6. PMID 27217474. doi:10.1093/abbs/gmw045.
- ↑ Botuyan MV, Lee J, Ward IM, Kim JE, Thompson JR, Chen J, Mer G (Dec 2006). "Structural basis for the methylation state-specific recognition of histone H4-K20 by 53BP1 and Crb2 in DNA repair". Cell 127 (7): 1361–73. PMC 1804291. PMID 17190600. doi:10.1016/j.cell.2006.10.043.
- ↑ Derbyshire DJ, Basu BP, Serpell LC, Joo WS, Date T, Iwabuchi K, Doherty AJ (Jul 2002). "Crystal structure of human 53BP1 BRCT domains bound to p53 tumour suppressor". The EMBO Journal 21 (14): 3863–72. PMC 126127. PMID 12110597. doi:10.1093/emboj/cdf383.
- ↑ Ekblad CM, Friedler A, Veprintsev D, Weinberg RL, Itzhaki LS (Mar 2004). "Comparison of BRCT domains of BRCA1 and 53BP1: a biophysical analysis". Protein Science 13 (3): 617–25. PMC 2286730. PMID 14978302. doi:10.1110/ps.03461404.
- ↑ Joo WS, Jeffrey PD, Cantor SB, Finnin MS, Livingston DM, Pavletich NP (Mar 2002). "Structure of the 53BP1 BRCT region bound to p53 and its comparison to the Brca1 BRCT structure". Genes & Development 16 (5): 583–93. PMC 155350. PMID 11877378. doi:10.1101/gad.959202.
- ↑ Derbyshire DJ, Basu BP, Date T, Iwabuchi K, Doherty AJ (Oct 2002). "Purification, crystallization and preliminary X-ray analysis of the BRCT domains of human 53BP1 bound to the p53 tumour suppressor". Acta Crystallographica Section D 58 (Pt 10 Pt 2): 1826–9. PMID 12351827. doi:10.1107/S0907444902010910.
- ↑ Lo KW, Kan HM, Chan LN, Xu WG, Wang KP, Wu Z, Sheng M, Zhang M (Mar 2005). "The 8-kDa dynein light chain binds to p53-binding protein 1 and mediates DNA damage-induced p53 nuclear accumulation". The Journal of Biological Chemistry 280 (9): 8172–9. PMID 15611139. doi:10.1074/jbc.M411408200.
Véxase tamén editar
Bibliografía editar
- Choubey D, Lengyel P (Mar 1995). "Binding of an interferon-inducible protein (p202) to the retinoblastoma protein". The Journal of Biological Chemistry 270 (11): 6134–40. PMID 7890747. doi:10.1074/jbc.270.11.6134.
- Choubey D, Li SJ, Datta B, Gutterman JU, Lengyel P (Oct 1996). "Inhibition of E2F-mediated transcription by p202". The EMBO Journal 15 (20): 5668–78. PMC 452311. PMID 8896460.
- Datta B, Li B, Choubey D, Nallur G, Lengyel P (Nov 1996). "p202, an interferon-inducible modulator of transcription, inhibits transcriptional activation by the p53 tumor suppressor protein, and a segment from the p53-binding protein 1 that binds to p202 overcomes this inhibition". The Journal of Biological Chemistry 271 (44): 27544–55. PMID 8910340. doi:10.1074/jbc.271.44.27544.
- Wen Y, Yan DH, Spohn B, Deng J, Lin SY, Hung MC (Jan 2000). "Tumor suppression and sensitization to tumor necrosis factor alpha-induced apoptosis by an interferon-inducible protein, p202, in breast cancer cells". Cancer Research 60 (1): 42–6. PMID 10646849.
- Xia Z, Morales JC, Dunphy WG, Carpenter PB (Jan 2001). "Negative cell cycle regulation and DNA damage-inducible phosphorylation of the BRCT protein 53BP1". The Journal of Biological Chemistry 276 (4): 2708–18. PMID 11042216. doi:10.1074/jbc.M007665200.
- Joo WS, Jeffrey PD, Cantor SB, Finnin MS, Livingston DM, Pavletich NP (Mar 2002). "Structure of the 53BP1 BRCT region bound to p53 and its comparison to the Brca1 BRCT structure". Genes & Development 16 (5): 583–93. PMC 155350. PMID 11877378. doi:10.1101/gad.959202.
- Derbyshire DJ, Basu BP, Serpell LC, Joo WS, Date T, Iwabuchi K, Doherty AJ (Jul 2002). "Crystal structure of human 53BP1 BRCT domains bound to p53 tumour suppressor". The EMBO Journal 21 (14): 3863–72. PMC 126127. PMID 12110597. doi:10.1093/emboj/cdf383.
- Lai H, Lin L, Nadji M, Lai S, Trapido E, Meng L (2002). "Mutations in the p53 tumor suppressor gene and early onset breast cancer". Cancer Biology & Therapy 1 (1): 31–6. PMID 12170762. doi:10.4161/cbt.1.1.37.
- Derbyshire DJ, Basu BP, Date T, Iwabuchi K, Doherty AJ (Oct 2002). "Purification, crystallization and preliminary X-ray analysis of the BRCT domains of human 53BP1 bound to the p53 tumour suppressor". Acta Crystallographica Section D 58 (Pt 10 Pt 2): 1826–9. PMID 12351827. doi:10.1107/S0907444902010910.
- Wang B, Matsuoka S, Carpenter PB, Elledge SJ (Nov 2002). "53BP1, a mediator of the DNA damage checkpoint". Science 298 (5597): 1435–8. PMID 12364621. doi:10.1126/science.1076182.
- Richie CT, Peterson C, Lu T, Hittelman WN, Carpenter PB, Legerski RJ (Dec 2002). "hSnm1 colocalizes and physically associates with 53BP1 before and after DNA damage". Molecular and Cellular Biology 22 (24): 8635–47. PMC 139863. PMID 12446782. doi:10.1128/MCB.22.24.8635-8647.2002.
- DiTullio RA, Mochan TA, Venere M, Bartkova J, Sehested M, Bartek J, Halazonetis TD (Dec 2002). "53BP1 functions in an ATM-dependent checkpoint pathway that is constitutively activated in human cancer". Nature Cell Biology 4 (12): 998–1002. PMID 12447382. doi:10.1038/ncb892.
- Fernandez-Capetillo O, Chen HT, Celeste A, Ward I, Romanienko PJ, Morales JC, Naka K, Xia Z, Camerini-Otero RD, Motoyama N, Carpenter PB, Bonner WM, Chen J, Nussenzweig A (Dec 2002). "DNA damage-induced G2-M checkpoint activation by histone H2AX and 53BP1". Nature Cell Biology 4 (12): 993–7. PMID 12447390. doi:10.1038/ncb884.
- Peng A, Chen PL (Mar 2003). "NFBD1, like 53BP1, is an early and redundant transducer mediating Chk2 phosphorylation in response to DNA damage". The Journal of Biological Chemistry 278 (11): 8873–6. PMID 12551934. doi:10.1074/jbc.C300001200.
- Stewart GS, Wang B, Bignell CR, Taylor AM, Elledge SJ (Feb 2003). "MDC1 is a mediator of the mammalian DNA damage checkpoint". Nature 421 (6926): 961–6. PMID 12607005. doi:10.1038/nature01446.
- Yan DH, Abramian A, Li Z, Ding Y, Wen Y, Liu TJ, Hunt K (Mar 2003). "P202, an interferon-inducible protein, inhibits E2F1-mediated apoptosis in prostate cancer cells". Biochemical and Biophysical Research Communications 303 (1): 219–22. PMID 12646190. doi:10.1016/S0006-291X(03)00320-6.
- Kao GD, McKenna WG, Guenther MG, Muschel RJ, Lazar MA, Yen TJ (Mar 2003). "Histone deacetylase 4 interacts with 53BP1 to mediate the DNA damage response". The Journal of Cell Biology 160 (7): 1017–27. PMC 2172769. PMID 12668657. doi:10.1083/jcb.200209065.
- Caldwell RB, Braselmann H, Schoetz U, Heuer S, Scherthan H, Zitzelsberger H (July 4, 2016). "Positive Cofactor 4 (PC4) is critical for DNA repair pathway re-routing in DT40 cells.". Sci. Rep. 6: 28890. PMC 4931448. PMID 27374870. doi:10.1038/srep28890.