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Dnmt3a binds deacetylases and is recruited by a sequence‐specific repressor to silence transcription

Fuks, François, Burgers, Wendy A., Godin, Nadia, Kasai, Masataka, Kouzarides, Tony·2001·The EMBO Journal

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Research works printed but not linked: 46

  1. Aapola U et al. (2000) Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22.3, related to the cytosine‐5‐methyltransferase 3 gene family. Genomics, 65, 293–298. · DOI
  2. Aasland R, Gibson TJ and Stewart AF (1995) The PHD finger: implications for chromatin‐mediated transcriptional regulation. Trends Biochem Sci, 20, 56–59. · DOI
  3. Aoki K, Meng G, Suzuki K, Takashi T, Kameoka Y, Nakahara K, Ishida R and Kasai M (1998) RP58 associates with condensed chromatin and mediates a sequence‐ specific transcriptional repression. J Biol Chem, 273, 26698–26704. · DOI
  4. Bannister AJ and Kouzarides T (1995) CBP‐induced stimulation of c‐Fos activity is abrogated by E1A. EMBO J, 14, 4758–4762. · DOI
  5. Bannister AJ and Kouzarides T (1996) The CBP co‐activator is a histone acetyltransferase. Nature, 384, 641–643. · DOI
  6. Bardwell VJ and Treisman R (1994) The POZ domain: a conserved protein–protein interaction motif. Genes Dev, 8, 1664–1677. · DOI
  7. Bestor TH (2000) The DNA methyltransferases of mammals. Hum Mol Genet, 9, 2395–2402. · DOI
  8. Bestor T, Laudano A, Mattaliano R and Ingram V (1988) Cloning and sequencing of a cDNA encoding DNA methyltransferase of mouse cells. The carboxyl‐terminal domain of the mammalian enzymes is related to bacterial restriction methyltransferases. J Mol Biol, 203, 971–983. · DOI
  9. Brehm A, Miska EA, McCance DJ, Reid JL, Bannister AJ and Kouzarides T (1998) Retinoblastoma protein recruits histone deacetylase to repress transcription. Nature, 391, 597–601. · DOI
  10. Brehm A, Nielsen SJ, Miska EA, McCance DJ, Reid JL, Bannister AJ and Kouzarides T (1999) The E7 oncoprotein associates with Mi2 and histone deacetylase activity to promote cell growth. EMBO J, 18, 2449–2458. · DOI · Paper page
  11. Cross SH, Meehan RR, Nan X and Bird A (1997) A component of the transcriptional repressor MeCP1 shares a motif with DNA methyltransferase and HRX proteins. Nature Genet, 16, 256–259. · DOI
  12. Fuks F, Burgers WA, Brehm A, Hughes‐Davies L and Kouzarides T (2000) DNA methyltransferase Dnmt1 associates with histone deacetylase activity. Nature Genet, 24, 88–91. · DOI
  13. Gibbons RJ et al. (1997) Mutations in transcriptional regulator ATRX establish the functional significance of a PHD‐like domain. Nature Genet, 17, 146–148. · DOI
  14. Hagemeier C, Cook A and Kouzarides T (1993) The retinoblastoma protein binds E2F residues required for activation in vivo and TBP binding in vitro. Nucleic Acids Res, 21, 4998–5004. · DOI
  15. Hsieh CL (1999) In vivo activity of murine de novo methyltransferases, Dnmt3a and Dnmt3b. Mol Cell Biol, 19, 8211–8218. · DOI
  16. Jaenisch R (1997) DNA methylation and imprinting: why bother? Trends Genet, 13, 323–329. · DOI
  17. Jones PL, Veenstra GJ, Wade PA, Vermaak D, Kass SU, Landsberger N, Strouboulis J and Wolffe AP (1998) Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription. Nature Genet, 19, 187–191. · DOI
  18. Kafri T, Ariel M, Brandeis M, Shemer R, Urven L, McCarrey J, Cedar H and Razin A (1992) Developmental pattern of gene‐specific DNA methylation in the mouse embryo and germ line. Genes Dev, 6, 705–714. · DOI
  19. Kouzarides T (1999) Histone acetylases and deacetylases in cell proliferation. Curr Opin Genet Dev, 9, 40–48. · DOI
  20. Lauster R, Trautner TA and Noyer‐Weidner M (1989) Cytosine‐specific type II DNA methyltransferases. A conserved enzyme core with variable target‐recognizing domains. J Mol Biol, 206, 305–312. · DOI
  21. Lavender P, Vandel L, Bannister AJ and Kouzarides T (1997) The HMG‐box transcription factor HBP1 is targeted by the pocket proteins and E1A. Oncogene, 14, 2721–2728. · DOI
  22. Leonhardt H, Page AW, Weier HU and Bestor TH (1992) A targeting sequence directs DNA methyltransferase to sites of DNA replication in mammalian nuclei. Cell, 71, 865–873. · DOI
  23. Liu Y, Oakeley EJ, Sun L and Jost JP (1998) Multiple domains are involved in the targeting of the mouse DNA methyltransferase to the DNA replication foci. Nucleic Acids Res, 26, 1038–1045. · DOI
  24. Lyko F, Ramsahoye BH, Kashevsky H, Tudor M, Mastrangelo MA, Orr‐Weaver TL and Jaenisch R (1999) Mammalian (cytosine‐5) methyltransferases cause genomic DNA methylation and lethality in Drosophila. Nature Genet, 23, 363–366. · DOI
  25. Ma Q et al. (1993) Analysis of the murine All‐1 gene reveals conserved domains with human ALL‐1 and identifies a motif shared with DNA methyltransferases. Proc Natl Acad Sci USA, 90, 6350–6354. · DOI
  26. Martinez‐Balbas MA, Bauer UM, Nielsen SJ, Brehm A and Kouzarides T (2000) Regulation of E2F1 activity by acetylation. EMBO J, 19, 662–671. · DOI
  27. Monk M, Boubelik M and Lehnert S (1987) Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development. Development, 99, 371–382. · DOI
  28. Morkel M, Wenkel J, Bannister AJ, Kouzarides T and Hagemeier C (1997) An E2F‐like repressor of transcription. Nature, 390, 567–568. · DOI
  29. Nan X, Ng HH, Johnson CA, Laherty CD, Turner BM, Eisenman RN and Bird A (1998) Transcriptional repression by the methyl‐CpG‐binding protein MeCP2 involves a histone deacetylase complex. Nature, 393, 386–389. · DOI · Paper page
  30. Ng HH, Zhang Y, Hendrich B, Johnson CA, Turner BM, Erdjument‐Bromage H, Tempst P, Reinberg D and Bird A (1999) MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase complex. Nature Genet, 23, 58–61. · DOI
  31. Ng HH, Jeppesen P and Bird A (2000) Active repression of methylated genes by the chromosomal protein MBD1. Mol Cell Biol, 20, 1394–1406. · DOI
  32. Okano M, Xie S and Li E (1998) Cloning and characterization of a family of novel mammalian DNA (cytosine‐5) methyltransferases. Nature Genet, 19, 219–220. · DOI
  33. Okano M, Bell DW, Haber DA and Li E (1999) DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. Cell, 99, 247–257. · DOI · Paper page
  34. Ramchandani S, MacLeod AR, Pinard M, von Hofe E and Szyf M (1997) Inhibition of tumorigenesis by a cytosine‐DNA, methyltransferase, antisense oligodeoxynucleotide. Proc Natl Acad Sci USA, 94, 684–689. · DOI
  35. Razin A (1998) CpG methylation, chromatin structure and gene silencing—a three‐way connection. EMBO J, 17, 4905–4908. · DOI
  36. Robertson KD, Ait‐Si‐Ali S, Yokochi T, Wade PA, Jones PL and Wolffe AP (2000) DNMT1 forms a complex with Rb, E2F1 and HDAC1 and represses transcription from E2F‐responsive promoters. Nature Genet, 25, 338–342. · DOI · Paper page
  37. Rountree MR, Bachman KE and Baylin SB (2000) DNMT1 binds HDAC2 and a new co‐repressor, DMAP1, to form a complex at replication foci. Nature Genet, 25, 269–277. · DOI
  38. Sanford JP, Clark HJ, Chapman VM and Rossant J (1987) Differences in DNA methylation during oogenesis and spermatogenesis and their persistence during early embryogenesis in the mouse. Genes Dev, 1, 1039–1046. · DOI
  39. Surani MA (1998) Imprinting and the initiation of gene silencing in the germ line. Cell, 93, 309–312. · DOI
  40. Vertino PM, Yen RW, Gao J and Baylin SB (1996) De novo methylation of CpG island sequences in human fibroblasts overexpressing DNA (cytosine‐5)‐methyltransferase. Mol Cell Biol, 16, 4555–4565. · DOI
  41. Wade PA, Gegonne A, Jones PL, Ballestar E, Aubry F and Wolffe AP (1999) Mi‐2 complex couples DNA methylation to chromatin remodelling and histone deacetylation. Nature Genet, 23, 62–66. · DOI
  42. Xu GL et al. (1999) Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene. Nature, 402, 187–191. · DOI
  43. Yoder JA, Soman NS, Verdine GL and Bestor TH (1997) DNA (cytosine‐5)‐methyltransferases in mouse cells and tissues. Studies with a mechanism‐based probe. J Mol Biol, 270, 385–395. · DOI
  44. Yoshida M, Horinouchi S and Beppu T (1995) Trichostatin A and trapoxin: novel chemical probes for the role of histone acetylation in chromatin structure and function. BioEssays, 17, 423–430. · DOI
  45. Zhang Y, LeRoy G, Seelig HP, Lane WS and Reinberg D (1998) The dermatomyositis‐specific autoantigen Mi2 is a component of a complex containing histone deacetylase and nucleosome remodeling activities. Cell, 95, 279–289. · DOI
  46. Zhang Y, Ng HH, Erdjument‐Bromage H, Tempst P, Bird A and Reinberg D (1999) Analysis of the NuRD subunits reveals a histone deacetylase core complex and a connection with DNA methylation. Genes Dev, 13, 1924–1935. · DOI · Paper page

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Metadata

Authors
Fuks, F., Burgers, W. A., Godin, N., Kasai, M., & Kouzarides, T.
Venue
The EMBO Journal
Published
2001-05-15
Volume
20
Issue
10
Pages
2536-2544
ISSN
  • 0261-4189
  • 1460-2075
Cited by
473
References
4
Language
en

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Fuks, F., Burgers, W. A., Godin, N., Kasai, M., & Kouzarides, T. (2001). Dnmt3a binds deacetylases and is recruited by a sequence‐specific repressor to silence transcription. The EMBO Journal. https://doi.org/10.1093/emboj/20.10.2536