CoREST is an integral component of the CoREST-human histone deacetylase complex

被引:393
作者
You, A
Tong, JK
Grozinger, CM
Schreiber, SL
机构
[1] Harvard Univ, Howard Hughes Med Inst, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Howard Hughes Med Inst, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
关键词
D O I
10.1073/pnas.98.4.1454
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Here we describe the components of a histone deacetylase (HDAC) complex that we term the CoREST-HDAC complex. CoREST-HDAC is composed of polypeptides distinct from previously characterized HDAC1/2-containing complexes such as the mSin3 and nucleosome remodeling and deacetylating (NRD, also named NURD, NuRD) complex. Interestingly, we do not observe RbAp46 and RbAp48 in this complex, although these proteins have been observed in all previously identified complexes and are thought to be part of an HDAC1/2 core. We identify the transcriptional corepressor CoREST and a protein with homology to polyamine oxidases as components of CoREST-HDAC. The HDAC1/2-interacting region of CoREST is mapped to a 179-aa region containing a SANT domain, a domain found in other HDAC1/2-interacting proteins such as NCoR, MTA1, and MTA2. Furthermore, we demonstrate that the corepressor function of CoREST depends on this region. Although CoREST initially was cloned as a corepressor to REST (RE1 silencing transcription factor/neural restrictive silencing factor), we find no evidence for the existence of the eight-zinc finger REST transcription factor as an interacting partner in this complex; however, we do find evidence for association of the putative oncogene ZNF 217 that contains eight zinc fingers.
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页码:1454 / 1458
页数:5
相关论文
共 20 条
  • [1] Aasland R, 1996, TRENDS BIOCHEM SCI, V21, P87, DOI 10.1016/0968-0004(96)30009-1
  • [2] CoREST:: A functional corepressor required for regulation of neural-specific gene expression
    Andrés, ME
    Burger, C
    Peral-Rubio, MJ
    Battaglioli, E
    Anderson, ME
    Grimes, J
    Dallman, J
    Ballas, N
    Mandel, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (17) : 9873 - 9878
  • [3] Positional cloning of ZNF217 and NABC1:: Genes amplified at 20q13.2 and overexpressed in breast carcinoma
    Collins, C
    Rommens, JM
    Kowbel, D
    Godfrey, T
    Tanner, M
    Hwang, S
    Polikoff, D
    Nonet, G
    Cochran, J
    Myambo, K
    Jay, KE
    Froula, J
    Cloutier, T
    Kuo, WL
    Yaswen, P
    Dairkee, S
    Giovanola, J
    Hutchinson, GB
    Isola, J
    Kallioniemi, OP
    Palazzolo, M
    Martin, C
    Ericsson, C
    Pinkel, D
    Albertson, D
    Li, WB
    Gray, JW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) : 8703 - 8708
  • [4] The co-repressor mSin3A is a functional component of the REST-CoREST repressor complex
    Grimes, JA
    Nielsen, SJ
    Battaglioli, E
    Miska, EA
    Speh, JC
    Berry, DL
    Atouf, F
    Holdener, BC
    Mandel, G
    Kouzarides, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (13) : 9461 - 9467
  • [5] A role for histone deacetylase activity in HDAC1-mediated transcriptional repression
    Hassig, CA
    Tong, JK
    Fleischer, TC
    Owa, T
    Grable, PG
    Ayer, DE
    Schreiber, SL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) : 3519 - 3524
  • [6] Histone deacetylase activity is required for full transcriptional repression by mSin3A
    Hassig, CA
    Fleischer, TC
    Billin, AN
    Schreiber, SL
    Ayer, DE
    [J]. CELL, 1997, 89 (03) : 341 - 347
  • [7] Nuclear histone acetylases and deacetylases and transcriptional regulation: HATs off to HDACs
    Hassig, CA
    Schreiber, SL
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 1997, 1 (03) : 300 - 308
  • [8] Transcriptional repression by REST: recruitment of Sin3A and histone deacetylase to neuronal genes
    Huang, YF
    Myers, SJ
    Dingledine, R
    [J]. NATURE NEUROSCIENCE, 1999, 2 (10) : 867 - 872
  • [9] HUMPHREY GW, 2000, J BIOL CHEM
  • [10] Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase
    Imai, S
    Armstrong, CM
    Kaeberlein, M
    Guarente, L
    [J]. NATURE, 2000, 403 (6771) : 795 - 800