Histona deacetilasa 1

Histona deacetilasa 1
Histona deacetilasa 1
HUGO 4852
Símbolo HDAC1
Símbolos alt. DKFZp686H12203; GON-10; HD1; RPD3; RPD3L1
Datos genéticos
Locus Cr. 1 p35.1
Bases de datos
Entrez 3065
OMIM 601241
RefSeq NP_004955
UniProt Q13547

La histona deacetilasa 1 (HDAC1) es una enzima codificada en humanos por el gen hdac1.[1]

Contenido

Función

Las histonas juegan un papel crucial en la regulación de la transcripción, en la progresión del ciclo celular y en procesos de desarrollo. La acetilación/desacetilación de histonas altera la estructura del cromosoma, variando así la accesibilidad de los factores de transcripción al ADN. La HDAC1 pertenece a la familia de histona deacetilasas acuc/alfa y es uno de los componentes del complejo histona deacetilasa. Esta proteína interacciona con la proteína del retinoblastoma formando un complejo que es un elemento clave en el control de la proliferación celular y la diferenciación celular. Junto con la proteína 2 asociada a metástasis, deacetila a p53 y modula su acción sobre la proliferación celular y la apoptosis.[2]

Interacciones

La histona deacetilasa 1 ha demostrado ser capaz de interaccionar con:

Véase también

Referencias

  1. ↑ Taunton J, Hassig CA, Schreiber SL (May 1996). «A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p». Science 272 (5260):  pp. 408–11. PMID 8602529. 
  2. ↑ «Entrez Gene: HDAC1 histone deacetylase 1».
  3. ↑ a b Cai, R L; Yan-Neale Y, Cueto M A, Xu H, Cohen D (Sep. 2000). «HDAC1, a histone deacetylase, forms a complex with Hus1 and Rad9, two G2/M checkpoint Rad proteins». J. Biol. Chem. (UNITED STATES) 275 (36):  pp. 27909–16. doi:10.1074/jbc.M000168200. ISSN 0021-9258. PMID 10846170. 
  4. ↑ Aapola, Ulla; Liiv Ingrid, Peterson Pärt (Aug. 2002). «Imprinting regulator DNMT3L is a transcriptional repressor associated with histone deacetylase activity». Nucleic Acids Res. (England) 30 (16):  pp. 3602–8. PMID 12177302. 
  5. ↑ Deplus, Rachel; Brenner Carmen, Burgers Wendy A, Putmans Pascale, Kouzarides Tony, de Launoit Yvan, Fuks François (Sep. 2002). «Dnmt3L is a transcriptional repressor that recruits histone deacetylase». Nucleic Acids Res. (England) 30 (17):  pp. 3831–8. PMID 12202768. 
  6. ↑ a b c d e f g Yao, Ya-Li; Yang Wen-Ming (Oct. 2003). «The metastasis-associated proteins 1 and 2 form distinct protein complexes with histone deacetylase activity». J. Biol. Chem. (United States) 278 (43):  pp. 42560–8. doi:10.1074/jbc.M302955200. ISSN 0021-9258. PMID 12920132. 
  7. ↑ Mazumdar, A; Wang R A, Mishra S K, Adam L, Bagheri-Yarmand R, Mandal M, Vadlamudi R K, Kumar R (Jan. 2001). «Transcriptional repression of oestrogen receptor by metastasis-associated protein 1 corepressor». Nat. Cell Biol. (England) 3 (1):  pp. 30–7. doi:10.1038/35050532. ISSN 1465-7392. PMID 11146623. 
  8. ↑ Yang, W M; Yao Y L, Seto E (Sep. 2001). «The FK506-binding protein 25 functionally associates with histone deacetylases and with transcription factor YY1». EMBO J. (England) 20 (17):  pp. 4814–25. doi:10.1093/emboj/20.17.4814. ISSN 0261-4189. PMID 11532945. 
  9. ↑ a b c d e f Yoon, Young-Mee; Baek Kwan-Hyuck, Jeong Sook-Jung, Shin Hyun-Jin, Ha Geun-Hyoung, Jeon Ae-Hwa, Hwang Sang-Gu, Chun Jang-Soo, Lee Chang-Woo (Sep. 2004). «WD repeat-containing mitotic checkpoint proteins act as transcriptional repressors during interphase». FEBS Lett. (Netherlands) 575 (1-3):  pp. 23–9. doi:10.1016/j.febslet.2004.07.089. ISSN 0014-5793. PMID 15388328. 
  10. ↑ Wysocka, Joanna; Myers Michael P, Laherty Carol D, Eisenman Robert N, Herr Winship (Apr. 2003). «Human Sin3 deacetylase and trithorax-related Set1/Ash2 histone H3-K4 methyltransferase are tethered together selectively by the cell-proliferation factor HCF-1». Genes Dev. (United States) 17 (7):  pp. 896–911. doi:10.1101/gad.252103. ISSN 0890-9369. PMID 12670868. 
  11. ↑ a b Fischer, Denise D; Cai Richard, Bhatia Umesh, Asselbergs Fred A M, Song Chuanzheng, Terry Robert, Trogani Nancy, Widmer Roland, Atadja Peter, Cohen Dalia (Feb. 2002). «Isolation and characterization of a novel class II histone deacetylase, HDAC10». J. Biol. Chem. (United States) 277 (8):  pp. 6656–66. doi:10.1074/jbc.M108055200. ISSN 0021-9258. PMID 11739383. 
  12. ↑ Underhill, C; Qutob M S, Yee S P, Torchia J (Dec. 2000). «A novel nuclear receptor corepressor complex, N-CoR, contains components of the mammalian SWI/SNF complex and the corepressor KAP-1». J. Biol. Chem. (UNITED STATES) 275 (51):  pp. 40463–70. doi:10.1074/jbc.M007864200. ISSN 0021-9258. PMID 11013263. 
  13. ↑ a b Koipally, J; Renold A, Kim J, Georgopoulos K (Jun. 1999). «Repression by Ikaros and Aiolos is mediated through histone deacetylase complexes». EMBO J. (ENGLAND) 18 (11):  pp. 3090–100. doi:10.1093/emboj/18.11.3090. ISSN 0261-4189. PMID 10357820. 
  14. ↑ Koipally, Joseph; Georgopoulos Katia (Aug. 2002). «A molecular dissection of the repression circuitry of Ikaros». J. Biol. Chem. (United States) 277 (31):  pp. 27697–705. doi:10.1074/jbc.M201694200. ISSN 0021-9258. PMID 12015313. 
  15. ↑ Joshi, Bharat; Ko Danette, Ordonez-Ercan Dalia, Chellappan Srikumar P (Dec. 2003). «A putative coiled-coil domain of prohibitin is sufficient to repress E2F1-mediated transcription and induce apoptosis». Biochem. Biophys. Res. Commun. (United States) 312 (2):  pp. 459–66. ISSN 0006-291X. PMID 14637159. 
  16. ↑ a b Wang, Sheng; Fusaro Gina, Padmanabhan Jaya, Chellappan Srikumar P (Dec. 2002). «Prohibitin co-localizes with Rb in the nucleus and recruits N-CoR and HDAC1 for transcriptional repression». Oncogene (England) 21 (55):  pp. 8388–96. doi:10.1038/sj.onc.1205944. ISSN 0950-9232. PMID 12466959. 
  17. ↑ Vinatzer, U; Taplick J, Seiser C, Fonatsch C, Wieser R (Sep. 2001). «The leukaemia-associated transcription factors EVI-1 and MDS1/EVI1 repress transcription and interact with histone deacetylase». Br. J. Haematol. (England) 114 (3):  pp. 566–73. ISSN 0007-1048. PMID 11552981. 
  18. ↑ Chakraborty, S; Senyuk V, Sitailo S, Chi Y, Nucifora G (Nov. 2001). «Interaction of EVI1 with cAMP-responsive element-binding protein-binding protein (CBP) and p300/CBP-associated factor (P/CAF) results in reversible acetylation of EVI1 and in co-localization in nuclear speckles». J. Biol. Chem. (United States) 276 (48):  pp. 44936–43. doi:10.1074/jbc.M106733200. ISSN 0021-9258. PMID 11568182. 
  19. ↑ a b Wilson, Brian J; Bates Gaynor J, Nicol Samantha M, Gregory David J, Perkins Neil D, Fuller-Pace Frances V (Aug. 2004). «The p68 and p72 DEAD box RNA helicases interact with HDAC1 and repress transcription in a promoter-specific manner». BMC Mol. Biol. (England) 5:  pp. 11. doi:10.1186/1471-2199-5-11. PMID 15298701. 
  20. ↑ Fuks, F; Burgers W A, Godin N, Kasai M, Kouzarides T (May. 2001). «Dnmt3a binds deacetylases and is recruited by a sequence-specific repressor to silence transcription». EMBO J. (England) 20 (10):  pp. 2536–44. doi:10.1093/emboj/20.10.2536. ISSN 0261-4189. PMID 11350943. 
  21. ↑ Wotton, D; Lo R S, Lee S, Massagué J (Apr. 1999). «A Smad transcriptional corepressor». Cell (UNITED STATES) 97 (1):  pp. 29–39. ISSN 0092-8674. PMID 10199400. 
  22. ↑ a b c d Hakimi, Mohamed-Ali; Bochar Daniel A, Chenoweth Josh, Lane William S, Mandel Gail, Shiekhattar Ramin (May. 2002). «A core-BRAF35 complex containing histone deacetylase mediates repression of neuronal-specific genes». Proc. Natl. Acad. Sci. U.S.A. (United States) 99 (11):  pp. 7420–5. doi:10.1073/pnas.112008599. ISSN 0027-8424. PMID 12032298. 
  23. ↑ Hakimi, Mohamed-Ali; Dong Yuanshu, Lane William S, Speicher David W, Shiekhattar Ramin (Feb. 2003). «A candidate X-linked mental retardation gene is a component of a new family of histone deacetylase-containing complexes». J. Biol. Chem. (United States) 278 (9):  pp. 7234–9. doi:10.1074/jbc.M208992200. ISSN 0021-9258. PMID 12493763. 
  24. ↑ Fischle, Wolfgang; Dequiedt Franck, Hendzel Michael J, Guenther Matthew G, Lazar Mitchell A, Voelter Wolfgang, Verdin Eric (Jan. 2002). «Enzymatic activity associated with class II HDACs is dependent on a multiprotein complex containing HDAC3 and SMRT/N-CoR». Mol. Cell (United States) 9 (1):  pp. 45–57. ISSN 1097-2765. PMID 11804585. 
  25. ↑ a b Johnson, Colin A; White Darren A, Lavender Jayne S, O'Neill Laura P, Turner Bryan M (Mar. 2002). «Human class I histone deacetylase complexes show enhanced catalytic activity in the presence of ATP and co-immunoprecipitate with the ATP-dependent chaperone protein Hsp70». J. Biol. Chem. (United States) 277 (11):  pp. 9590–7. doi:10.1074/jbc.M107942200. ISSN 0021-9258. PMID 11777905. 
  26. ↑ Fischle, W; Dequiedt F, Fillion M, Hendzel M J, Voelter W, Verdin E (Sep. 2001). «Human HDAC7 histone deacetylase activity is associated with HDAC3 in vivo». J. Biol. Chem. (United States) 276 (38):  pp. 35826–35. doi:10.1074/jbc.M104935200. ISSN 0021-9258. PMID 11466315. 
  27. ↑ a b Ashburner, B P; Westerheide S D, Baldwin A S (Oct. 2001). «The p65 (RelA) subunit of NF-kappaB interacts with the histone deacetylase (HDAC) corepressors HDAC1 and HDAC2 to negatively regulate gene expression». Mol. Cell. Biol. (United States) 21 (20):  pp. 7065–77. doi:10.1128/MCB.21.20.7065-7077.2001. ISSN 0270-7306. PMID 11564889. 
  28. ↑ a b c d e f g h i Zhang, Y; Ng H H, Erdjument-Bromage H, Tempst P, Bird A, Reinberg D (Aug. 1999). «Analysis of the NuRD subunits reveals a histone deacetylase core complex and a connection with DNA methylation». Genes Dev. (UNITED STATES) 13 (15):  pp. 1924–35. ISSN 0890-9369. PMID 10444591. 
  29. ↑ a b c d Tong, J K; Hassig C A, Schnitzler G R, Kingston R E, Schreiber S L (Oct. 1998). «Chromatin deacetylation by an ATP-dependent nucleosome remodelling complex». Nature (ENGLAND) 395 (6705):  pp. 917–21. doi:10.1038/27699. ISSN 0028-0836. PMID 9804427. 
  30. ↑ a b c Hassig, C A; Tong J K, Fleischer T C, Owa T, Grable P G, Ayer D E, Schreiber S L (Mar. 1998). «A role for histone deacetylase activity in HDAC1-mediated transcriptional repression». Proc. Natl. Acad. Sci. U.S.A. (UNITED STATES) 95 (7):  pp. 3519–24. ISSN 0027-8424. PMID 9520398. 
  31. ↑ a b c Zhang, Y; Iratni R, Erdjument-Bromage H, Tempst P, Reinberg D (May. 1997). «Histone deacetylases and SAP18, a novel polypeptide, are components of a human Sin3 complex». Cell (UNITED STATES) 89 (3):  pp. 357–64. ISSN 0092-8674. PMID 9150135. 
  32. ↑ a b c van der Vlag, J; Otte A P (Dec. 1999). «Transcriptional repression mediated by the human polycomb-group protein EED involves histone deacetylation». Nat. Genet. (UNITED STATES) 23 (4):  pp. 474–8. doi:10.1038/70602. ISSN 1061-4036. PMID 10581039. 
  33. ↑ Ding, Zhihu; Gillespie Laura L, Paterno Gary D (Jan. 2003). «Human MI-ER1 alpha and beta function as transcriptional repressors by recruitment of histone deacetylase 1 to their conserved ELM2 domain». Mol. Cell. Biol. (United States) 23 (1):  pp. 250–8. ISSN 0270-7306. PMID 12482978. 
  34. ↑ a b Zhang, Ying; Dufau Maria L (Jun. 2003). «Dual mechanisms of regulation of transcription of luteinizing hormone receptor gene by nuclear orphan receptors and histone deacetylase complexes». J. Steroid Biochem. Mol. Biol. (England) 85 (2-5):  pp. 401–14. ISSN 0960-0760. PMID 12943729. 
  35. ↑ a b Fleischer, Tracey C; Yun Ui Jeong, Ayer Donald E (May. 2003). «Identification and characterization of three new components of the mSin3A corepressor complex». Mol. Cell. Biol. (United States) 23 (10):  pp. 3456–67. ISSN 0270-7306. PMID 12724404. 
  36. ↑ Yang, Liu; Mei Qi, Zielinska-Kwiatkowska Anna, Matsui Yoshito, Blackburn Michael L, Benedetti Daniel, Krumm Anton A, Taborsky Gerald J, Chansky Howard A (Feb. 2003). «An ERG (ets-related gene)-associated histone methyltransferase interacts with histone deacetylases 1/2 and transcription co-repressors mSin3A/B». Biochem. J. (England) 369 (Pt 3):  pp. 651–7. doi:10.1042/BJ20020854. ISSN 0264-6021. PMID 12398767. 
  37. ↑ a b c Grozinger, C M; Hassig C A, Schreiber S L (Apr. 1999). «Three proteins define a class of human histone deacetylases related to yeast Hda1p». Proc. Natl. Acad. Sci. U.S.A. (UNITED STATES) 96 (9):  pp. 4868–73. ISSN 0027-8424. PMID 10220385. 
  38. ↑ Zhang, Jinsong; Kalkum Markus, Chait Brian T, Roeder Robert G (Mar. 2002). «The N-CoR-HDAC3 nuclear receptor corepressor complex inhibits the JNK pathway through the integral subunit GPS2». Mol. Cell (United States) 9 (3):  pp. 611–23. ISSN 1097-2765. PMID 11931768. 
  39. ↑ a b c d You, A; Tong J K, Grozinger C M, Schreiber S L (Feb. 2001). «CoREST is an integral component of the CoREST- human histone deacetylase complex». Proc. Natl. Acad. Sci. U.S.A. (United States) 98 (4):  pp. 1454–8. doi:10.1073/pnas.98.4.1454. ISSN 0027-8424. PMID 11171972. 
  40. ↑ a b c Zhang, Ying; Dufau Maria L (Sep. 2002). «Silencing of transcription of the human luteinizing hormone receptor gene by histone deacetylase-mSin3A complex». J. Biol. Chem. (United States) 277 (36):  pp. 33431–8. doi:10.1074/jbc.M204417200. ISSN 0021-9258. PMID 12091390. 
  41. ↑ a b c Yasui, Dag; Miyano Masaru, Cai Shutao, Varga-Weisz Patrick, Kohwi-Shigematsu Terumi (Oct. 2002). «SATB1 targets chromatin remodelling to regulate genes over long distances». Nature (England) 419 (6907):  pp. 641–5. doi:10.1038/nature01084. ISSN 0028-0836. PMID 12374985. 
  42. ↑ Huang, E Y; Zhang J, Miska E A, Guenther M G, Kouzarides T, Lazar M A (Jan. 2000). «Nuclear receptor corepressors partner with class II histone deacetylases in a Sin3-independent repression pathway». Genes Dev. (UNITED STATES) 14 (1):  pp. 45–54. ISSN 0890-9369. PMID 10640275. 
  43. ↑ a b c d Kuzmichev, A; Zhang Y, Erdjument-Bromage H, Tempst P, Reinberg D (Feb. 2002). «Role of the Sin3-histone deacetylase complex in growth regulation by the candidate tumor suppressor p33(ING1)». Mol. Cell. Biol. (United States) 22 (3):  pp. 835–48. ISSN 0270-7306. PMID 11784859. 
  44. ↑ Li, H; Leo C, Zhu J, Wu X, O'Neil J, Park E J, Chen J D (Mar. 2000). «Sequestration and inhibition of Daxx-mediated transcriptional repression by PML». Mol. Cell. Biol. (UNITED STATES) 20 (5):  pp. 1784–96. ISSN 0270-7306. PMID 10669754. 
  45. ↑ Gaughan, Luke; Logan Ian R, Cook Susan, Neal David E, Robson Craig N (Jul. 2002). «Tip60 and histone deacetylase 1 regulate androgen receptor activity through changes to the acetylation status of the receptor». J. Biol. Chem. (United States) 277 (29):  pp. 25904–13. doi:10.1074/jbc.M203423200. ISSN 0021-9258. PMID 11994312. 
  46. ↑ Vietor, Ilja; Vadivelu Santhosh K, Wick Nikolaus, Hoffman Robert, Cotten Matt, Seiser Christian, Fialka Irene, Wunderlich Winfried, Haase Astrid, Korinkova Gabriela, Brosch Gerald, Huber Lukas A (Sep. 2002). «TIS7 interacts with the mammalian SIN3 histone deacetylase complex in epithelial cells». EMBO J. (England) 21 (17):  pp. 4621–31. ISSN 0261-4189. PMID 12198164. 
  47. ↑ Xia, Zhen-Biao; Anderson Melanie, Diaz Manuel O, Zeleznik-Le Nancy J (Jul. 2003). «MLL repression domain interacts with histone deacetylases, the polycomb group proteins HPC2 and BMI-1, and the corepressor C-terminal-binding protein». Proc. Natl. Acad. Sci. U.S.A. (United States) 100 (14):  pp. 8342–7. doi:10.1073/pnas.1436338100. ISSN 0027-8424. PMID 12829790. 
  48. ↑ Vieyra, Diego; Loewith Robbie, Scott Michelle, Bonnefin Paul, Boisvert Francois-Michel, Cheema Parneet, Pastyryeva Svitlana, Meijer Maria, Johnston Randal N, Bazett-Jones David P, McMahon Steven, Cole Michael D, Young Dallan, Riabowol Karl (Aug. 2002). «Human ING1 proteins differentially regulate histone acetylation». J. Biol. Chem. (United States) 277 (33):  pp. 29832–9. doi:10.1074/jbc.M200197200. ISSN 0021-9258. PMID 12015309. 
  49. ↑ a b Puri, P L; Iezzi S, Stiegler P, Chen T T, Schiltz R L, Muscat G E, Giordano A, Kedes L, Wang J Y, Sartorelli V (Oct. 2001). «Class I histone deacetylases sequentially interact with MyoD and pRb during skeletal myogenesis». Mol. Cell (United States) 8 (4):  pp. 885–97. ISSN 1097-2765. PMID 12479798. 
  50. ↑ Mal, A; Sturniolo M, Schiltz R L, Ghosh M K, Harter M L (Apr. 2001). «A role for histone deacetylase HDAC1 in modulating the transcriptional activity of MyoD: inhibition of the myogenic program». EMBO J. (England) 20 (7):  pp. 1739–53. doi:10.1093/emboj/20.7.1739. ISSN 0261-4189. PMID 11285237. 
  51. ↑ Watamoto, Kouichi; Towatari Masayuki, Ozawa Yukiyasu, Miyata Yasuhiko, Okamoto Mitsunori, Abe Akihiro, Naoe Tomoki, Saito Hidehiko (Dec. 2003). «Altered interaction of HDAC5 with GATA-1 during MEL cell differentiation». Oncogene (England) 22 (57):  pp. 9176–84. doi:10.1038/sj.onc.1206902. ISSN 0950-9232. PMID 14668799. 
  52. ↑ Shi, Y; Downes M, Xie W, Kao H Y, Ordentlich P, Tsai C C, Hon M, Evans R M (May. 2001). «Sharp, an inducible cofactor that integrates nuclear receptor repression and activation». Genes Dev. (United States) 15 (9):  pp. 1140–51. doi:10.1101/gad.871201. ISSN 0890-9369. PMID 11331609. 
  53. ↑ Khan, M M; Nomura T, Kim H, Kaul S C, Wadhwa R, Shinagawa T, Ichikawa-Iwata E, Zhong S, Pandolfi P P, Ishii S (Jun. 2001). «Role of PML and PML-RARalpha in Mad-mediated transcriptional repression». Mol. Cell (United States) 7 (6):  pp. 1233–43. ISSN 1097-2765. PMID 11430826. 
  54. ↑ Wu, W S; Vallian S, Seto E, Yang W M, Edmondson D, Roth S, Chang K S (Apr. 2001). «The growth suppressor PML represses transcription by functionally and physically interacting with histone deacetylases». Mol. Cell. Biol. (United States) 21 (7):  pp. 2259–68. doi:10.1128/MCB.21.7.2259-2268.2001. ISSN 0270-7306. PMID 11259576. 
  55. ↑ a b Melhuish, T A; Wotton D (Dec. 2000). «The interaction of the carboxyl terminus-binding protein with the Smad corepressor TGIF is disrupted by a holoprosencephaly mutation in TGIF». J. Biol. Chem. (UNITED STATES) 275 (50):  pp. 39762–6. doi:10.1074/jbc.C000416200. ISSN 0021-9258. PMID 10995736. 
  56. ↑ Melhuish, T A; Gallo C M, Wotton D (Aug. 2001). «TGIF2 interacts with histone deacetylase 1 and represses transcription». J. Biol. Chem. (United States) 276 (34):  pp. 32109–14. doi:10.1074/jbc.M103377200. ISSN 0021-9258. PMID 11427533. 
  57. ↑ a b c Ferreira, R; Magnaghi-Jaulin L, Robin P, Harel-Bellan A, Trouche D (Sep. 1998). «The three members of the pocket proteins family share the ability to repress E2F activity through recruitment of a histone deacetylase». Proc. Natl. Acad. Sci. U.S.A. (UNITED STATES) 95 (18):  pp. 10493–8. ISSN 0027-8424. PMID 9724731. 
  58. ↑ Bouzahzah, B; Fu M, Iavarone A, Factor V M, Thorgeirsson S S, Pestell R G (Aug. 2000). «Transforming growth factor-beta1 recruits histone deacetylase 1 to a p130 repressor complex in transgenic mice in vivo». Cancer Res. (UNITED STATES) 60 (16):  pp. 4531–7. ISSN 0008-5472. PMID 10969803. 
  59. ↑ a b Lai, A; Lee J M, Yang W M, DeCaprio J A, Kaelin W G, Seto E, Branton P E (Oct. 1999). «RBP1 recruits both histone deacetylase-dependent and -independent repression activities to retinoblastoma family proteins». Mol. Cell. Biol. (UNITED STATES) 19 (10):  pp. 6632–41. ISSN 0270-7306. PMID 10490602. 
  60. ↑ a b c Ng, H H; Zhang Y, Hendrich B, Johnson C A, Turner B M, Erdjument-Bromage H, Tempst P, Reinberg D, Bird A (Sep. 1999). «MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase complex». Nat. Genet. (UNITED STATES) 23 (1):  pp. 58–61. doi:10.1038/12659. ISSN 1061-4036. PMID 10471484. 
  61. ↑ Anderson, Lisa A; Perkins Neil D (Aug. 2002). «The large subunit of replication factor C interacts with the histone deacetylase, HDAC1». J. Biol. Chem. (United States) 277 (33):  pp. 29550–4. doi:10.1074/jbc.M200513200. ISSN 0021-9258. PMID 12045192. 
  62. ↑ Dick, F A; Sailhamer E, Dyson N J (May. 2000). «Mutagenesis of the pRB pocket reveals that cell cycle arrest functions are separable from binding to viral oncoproteins». Mol. Cell. Biol. (UNITED STATES) 20 (10):  pp. 3715–27. ISSN 0270-7306. PMID 10779361. 
  63. ↑ Fuks, F; Burgers W A, Brehm A, Hughes-Davies L, Kouzarides T (Jan. 2000). «DNA methyltransferase Dnmt1 associates with histone deacetylase activity». Nat. Genet. (UNITED STATES) 24 (1):  pp. 88–91. doi:10.1038/71750. ISSN 1061-4036. PMID 10615135. 
  64. ↑ Luo, R X; Postigo A A, Dean D C (Feb. 1998). «Rb interacts with histone deacetylase to repress transcription». Cell (UNITED STATES) 92 (4):  pp. 463–73. ISSN 0092-8674. PMID 9491888. 
  65. ↑ Nicolas, E; Ait-Si-Ali S, Trouche D (Aug. 2001). «The histone deacetylase HDAC3 targets RbAp48 to the retinoblastoma protein». Nucleic Acids Res. (England) 29 (15):  pp. 3131–6. PMID 11470869. 
  66. ↑ Hassig, C A; Fleischer T C, Billin A N, Schreiber S L, Ayer D E (May. 1997). «Histone deacetylase activity is required for full transcriptional repression by mSin3A». Cell (UNITED STATES) 89 (3):  pp. 341–7. ISSN 0092-8674. PMID 9150133. 
  67. ↑ Iwase, Shigeki; Januma Aya, Miyamoto Kiyoko, Shono Naomi, Honda Arata, Yanagisawa Junn, Baba Tadashi (Sep. 2004). «Characterization of BHC80 in BRAF-HDAC complex, involved in neuron-specific gene repression». Biochem. Biophys. Res. Commun. (United States) 322 (2):  pp. 601–8. doi:10.1016/j.bbrc.2004.07.163. ISSN 0006-291X. PMID 15325272. 
  68. ↑ Kiernan, Rosemary; Brès Vanessa, Ng Raymond W M, Coudart Marie-Pierre, El Messaoudi Selma, Sardet Claude, Jin Dong-Yan, Emiliani Stephane, Benkirane Monsef (Jan. 2003). «Post-activation turn-off of NF-kappa B-dependent transcription is regulated by acetylation of p65». J. Biol. Chem. (United States) 278 (4):  pp. 2758–66. doi:10.1074/jbc.M209572200. ISSN 0021-9258. PMID 12419806. 
  69. ↑ a b Zhong, Haihong; May Michael J, Jimi Eijiro, Ghosh Sankar (Mar. 2002). «The phosphorylation status of nuclear NF-kappa B determines its association with CBP/p300 or HDAC-1». Mol. Cell (United States) 9 (3):  pp. 625–36. ISSN 1097-2765. PMID 11931769. 
  70. ↑ Ito, Akihiro; Kawaguchi Yoshiharu, Lai Chun-Hsiang, Kovacs Jeffrey J, Higashimoto Yuichiro, Appella Ettore, Yao Tso-Pang (Nov. 2002). «MDM2-HDAC1-mediated deacetylation of p53 is required for its degradation». EMBO J. (England) 21 (22):  pp. 6236–45. ISSN 0261-4189. PMID 12426395. 
  71. ↑ Vaute, Olivier; Nicolas Estelle, Vandel Laurence, Trouche Didier (Jan. 2002). «Functional and physical interaction between the histone methyl transferase Suv39H1 and histone deacetylases». Nucleic Acids Res. (England) 30 (2):  pp. 475–81. PMID 11788710. 
  72. ↑ Brackertz, Marc; Boeke Joern, Zhang Ru, Renkawitz Rainer (Oct. 2002). «Two highly related p66 proteins comprise a new family of potent transcriptional repressors interacting with MBD2 and MBD3». J. Biol. Chem. (United States) 277 (43):  pp. 40958–66. doi:10.1074/jbc.M207467200. ISSN 0021-9258. PMID 12183469. 
  73. ↑ Chauchereau, Anne; Mathieu Marion, de Saintignon Julie, Ferreira Roger, Pritchard Linda L, Mishal Zohair, Dejean Anne, Harel-Bellan Annick (Nov. 2004). «HDAC4 mediates transcriptional repression by the acute promyelocytic leukaemia-associated protein PLZF». Oncogene (England) 23 (54):  pp. 8777–84. doi:10.1038/sj.onc.1208128. ISSN 0950-9232. PMID 15467736. 
  74. ↑ a b David, G; Alland L, Hong S H, Wong C W, DePinho R A, Dejean A (May. 1998). «Histone deacetylase associated with mSin3A mediates repression by the acute promyelocytic leukemia-associated PLZF protein». Oncogene (ENGLAND) 16 (19):  pp. 2549–56. doi:10.1038/sj.onc.1202043. ISSN 0950-9232. PMID 9627120. 
  75. ↑ Wong, C W; Privalsky M L (Oct. 1998). «Components of the SMRT corepressor complex exhibit distinctive interactions with the POZ domain oncoproteins PLZF, PLZF-RARalpha, and BCL-6». J. Biol. Chem. (UNITED STATES) 273 (42):  pp. 27695–702. ISSN 0021-9258. PMID 9765306. 
  76. ↑ Deltour, S; Guerardel C, Leprince D (Dec. 1999). «Recruitment of SMRT/N-CoR-mSin3A-HDAC-repressing complexes is not a general mechanism for BTB/POZ transcriptional repressors: the case of HIC-1 and gammaFBP-B». Proc. Natl. Acad. Sci. U.S.A. (UNITED STATES) 96 (26):  pp. 14831–6. ISSN 0027-8424. PMID 10611298. 
  77. ↑ Alland, Leila; David Gregory, Shen-Li Hong, Potes Jason, Muhle Rebecca, Lee Hye-Chun, Hou Harry, Chen Ken, DePinho Ronald A (Apr. 2002). «Identification of mammalian Sds3 as an integral component of the Sin3/histone deacetylase corepressor complex». Mol. Cell. Biol. (United States) 22 (8):  pp. 2743–50. ISSN 0270-7306. PMID 11909966. 
  78. ↑ Huang, Nu En; Lin Ching Hui, Lin Young Sun, Yu Winston C Y (Jun. 2003). «Modulation of YY1 activity by SAP30». Biochem. Biophys. Res. Commun. (United States) 306 (1):  pp. 267–75. ISSN 0006-291X. PMID 12788099. 
  79. ↑ Zhang, Y; Sun Z W, Iratni R, Erdjument-Bromage H, Tempst P, Hampsey M, Reinberg D (Jun. 1998). «SAP30, a novel protein conserved between human and yeast, is a component of a histone deacetylase complex». Mol. Cell (UNITED STATES) 1 (7):  pp. 1021–31. ISSN 1097-2765. PMID 9651585. 
  80. ↑ Swanson, Kurt A; Knoepfler Paul S, Huang Kai, Kang Richard S, Cowley Shaun M, Laherty Carol D, Eisenman Robert N, Radhakrishnan Ishwar (Aug. 2004). «HBP1 and Mad1 repressors bind the Sin3 corepressor PAH2 domain with opposite helical orientations». Nat. Struct. Mol. Biol. (United States) 11 (8):  pp. 738–46. doi:10.1038/nsmb798. ISSN 1545-9993. PMID 15235594. 
  81. ↑ Yochum, G S; Ayer D E (Jul. 2001). «Pf1, a novel PHD zinc finger protein that links the TLE corepressor to the mSin3A-histone deacetylase complex». Mol. Cell. Biol. (United States) 21 (13):  pp. 4110–8. doi:10.1128/MCB.21.13.4110-4118.2001. ISSN 0270-7306. PMID 11390640. 
  82. ↑ Di Padova, Monica; Bruno Tiziana, De Nicola Francesca, Iezzi Simona, D'Angelo Carmen, Gallo Rita, Nicosia Daniela, Corbi Nicoletta, Biroccio Annamaria, Floridi Aristide, Passananti Claudio, Fanciulli Maurizio (Sep. 2003). «Che-1 arrests human colon carcinoma cell proliferation by displacing HDAC1 from the p21WAF1/CIP1 promoter». J. Biol. Chem. (United States) 278 (38):  pp. 36496–504. doi:10.1074/jbc.M306694200. ISSN 0021-9258. PMID 12847090. 
  83. ↑ Singh, Jarnail; Murata Kenji, Itahana Yoko, Desprez Pierre-Yves (Mar. 2002). «Constitutive expression of the Id-1 promoter in human metastatic breast cancer cells is linked with the loss of NF-1/Rb/HDAC-1 transcription repressor complex». Oncogene (England) 21 (12):  pp. 1812–22. doi:10.1038/sj.onc.1205252. ISSN 0950-9232. PMID 11896613. 
  84. ↑ Sun, Jian-Min; Chen Hou Yu, Moniwa Mariko, Litchfield David W, Seto Edward, Davie James R (Sep. 2002). «The transcriptional repressor Sp3 is associated with CK2-phosphorylated histone deacetylase 2». J. Biol. Chem. (United States) 277 (39):  pp. 35783–6. doi:10.1074/jbc.C200378200. ISSN 0021-9258. PMID 12176973. 
  85. ↑ Milutinovic, Snezana; Zhuang Qianli, Szyf Moshe (Jun. 2002). «Proliferating cell nuclear antigen associates with histone deacetylase activity, integrating DNA replication and chromatin modification». J. Biol. Chem. (United States) 277 (23):  pp. 20974–8. doi:10.1074/jbc.M202504200. ISSN 0021-9258. PMID 11929879. 
  86. ↑ Hoogeveen, André T; Rossetti Stefano, Stoyanova Violeta, Schonkeren Joris, Fenaroli Angelia, Schiaffonati Luisa, van Unen Leontine, Sacchi Nicoletta (Sep. 2002). «The transcriptional corepressor MTG16a contains a novel nucleolar targeting sequence deranged in t (16; 21)-positive myeloid malignancies». Oncogene (England) 21 (43):  pp. 6703–12. doi:10.1038/sj.onc.1205882. ISSN 0950-9232. PMID 12242670. 
  87. ↑ Amann, J M; Nip J, Strom D K, Lutterbach B, Harada H, Lenny N, Downing J R, Meyers S, Hiebert S W (Oct. 2001). «ETO, a target of t(8;21) in acute leukemia, makes distinct contacts with multiple histone deacetylases and binds mSin3A through its oligomerization domain». Mol. Cell. Biol. (United States) 21 (19):  pp. 6470–83. ISSN 0270-7306. PMID 11533236. 
  88. ↑ a b Tsai, S C; Valkov N, Yang W M, Gump J, Sullivan D, Seto E (Nov. 2000). «Histone deacetylase interacts directly with DNA topoisomerase II». Nat. Genet. (UNITED STATES) 26 (3):  pp. 349–53. doi:10.1038/81671. ISSN 1061-4036. PMID 11062478. 
  89. ↑ a b Johnson, C A; Padget K, Austin C A, Turner B M (Feb. 2001). «Deacetylase activity associates with topoisomerase II and is necessary for etoposide-induced apoptosis». J. Biol. Chem. (United States) 276 (7):  pp. 4539–42. doi:10.1074/jbc.C000824200. ISSN 0021-9258. PMID 11136718. 
  90. ↑ Sakai, Hirotaka; Urano Takeshi, Ookata Kayoko, Kim Mi-Hyun, Hirai Yugo, Saito Motoki, Nojima Yoshihisa, Ishikawa Fuyuki (Dec. 2002). «MBD3 and HDAC1, two components of the NuRD complex, are localized at Aurora-A-positive centrosomes in M phase». J. Biol. Chem. (United States) 277 (50):  pp. 48714–23. doi:10.1074/jbc.M208461200. ISSN 0021-9258. PMID 12354758. 
  91. ↑ Saito, Motoki; Ishikawa Fuyuki (Sep. 2002). «The mCpG-binding domain of human MBD3 does not bind to mCpG but interacts with NuRD/Mi2 components HDAC1 and MTA2». J. Biol. Chem. (United States) 277 (38):  pp. 35434–9. doi:10.1074/jbc.M203455200. ISSN 0021-9258. PMID 12124384. 
  92. ↑ Zhang, C L; McKinsey T A, Lu J R, Olson E N (Jan. 2001). «Association of COOH-terminal-binding protein (CtBP) and MEF2-interacting transcription repressor (MITR) contributes to transcriptional repression of the MEF2 transcription factor». J. Biol. Chem. (UNITED STATES) 276 (1):  pp. 35–9. doi:10.1074/jbc.M007364200. ISSN 0021-9258. PMID 11022042. 
  93. ↑ Sundqvist, A; Sollerbrant K, Svensson C (Jun. 1998). «The carboxy-terminal region of adenovirus E1A activates transcription through targeting of a C-terminal binding protein-histone deacetylase complex». FEBS Lett. (NETHERLANDS) 429 (2):  pp. 183–8. ISSN 0014-5793. PMID 9650586. 
  94. ↑ Smirnov, D A; Hou S, Ricciardi R P (Mar. 2000). «Association of histone deacetylase with COUP-TF in tumorigenic Ad12-transformed cells and its potential role in shut-off of MHC class I transcription». Virology (UNITED STATES) 268 (2):  pp. 319–28. doi:10.1006/viro.1999.0181. ISSN 0042-6822. PMID 10704340. 

Enlaces externos


Wikimedia foundation. 2010.

Игры ⚽ Поможем написать курсовую

Mira otros diccionarios:

  • Histona deacetilasa — Identificadores Número EC 3.5.1.98 Bases de datos IntEnz …   Wikipedia Español

  • Histona deacetilasa 2 — HUGO 4853 Símbolo HDAC2 Símbolos alt. RPD3; YAF1 …   Wikipedia Español

  • Histona deacetilasa 3 — HUGO 4854 Símbolo HDAC3 Símbolos alt. RPD3; HD3; RPD3 2 …   Wikipedia Español

  • Histona deacetilasa 5 — HUGO 14068 Símbolo HDAC5 Símbolos alt. FLJ90614, HD5, NY CO 9 …   Wikipedia Español

  • Histona deacetilasa 9 — HUGO 14065 Símbolo HDAC9 Símbolos alt. DKFZp779K1053; HD7; HDAC; HDAC7; HDAC7B; HDAC9B; HDAC9FL; HDR …   Wikipedia Español

  • Histona deacetilasa 4 — Estructura tridimensional de la proteína HDAC4. HUGO 14063 …   Wikipedia Español

  • Histona deacetilasa 7A — Estructura tridimensional de la proteína HDAC7A. HUGO …   Wikipedia Español

  • Histona deacetilasa 10 — HUGO 18128 Símbolo HDAC10 Símbolos alt. DKFZP761B039; MGC149722 …   Wikipedia Español

  • inhibidores de la histona deacetilasa — una familia de fármacos, en fase de desarrollo, capaces de bloquear la angiogenesis y el ciclo celular y promover la apoptosis y diferenciación. Estos fármacos tienen una utilidad potencial como citostáticos Diccionario ilustrado de Términos… …   Diccionario médico

  • Histona acetiltransferasa — Identificadores Número EC 2.3.1.48 Número CAS 9054 51 7 …   Wikipedia Español

Compartir el artículo y extractos

Link directo
… Do a right-click on the link above
and select “Copy Link”