Calcium regulates transcriptional repression of myocyte enhancer factor 2 by histone deacetylase 4

被引:131
作者
Youn, HD
Grozinger, CM
Liu, JO
机构
[1] MIT, Dept Chem & Biol, Canc Res Ctr, Cambridge, MA 02139 USA
[2] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
关键词
D O I
10.1074/jbc.C000304200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The myocyte enhancer factor 2 (MEF2) consists of a family of transcription factors that play important roles in a number of physiological processes from muscle cell differentiation to neuronal survival and T cell apoptosis. MEF2 has been reported to be associated with several distinct repressors including Cabin1(cain), MEF2-interacting transcriptional repressor (MITR), and HDAC4. It has been previously shown that Cabin1 is associated with MEF2 in a calcium-sensitive manner; activated calmodulin binds to Cabin1 and releases it from MEF2. However, it was not known whether the binding of HDAC4 and MITR to MEF2 is also regulated by calcium. We report that HDAC4 and MITR contain calmodulin-binding domains that overlap with their MEF2-binding domains. Binding of calmodulin to HDAC4 leads to its dissociation from MEF2, relieving MEF2 from the transcriptional repression by HDAC4. Together, HDAC4, MITE, and Cabin1 constitute a family of calcium-sensitive transcriptional repressors of MEF2.
引用
收藏
页码:22563 / 22567
页数:5
相关论文
共 40 条
  • [21] Signal-dependent activation of the MEF2 transcription factor by dissociation from histone deacetylases
    Lu, JR
    McKinsey, TA
    Nicol, RL
    Olson, EN
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (08) : 4070 - 4075
  • [22] Retinoblastoma protein represses transcription by recruiting a histone deacetylase
    Magnaghi-Jaulin, L
    Groisman, R
    Naguibneva, I
    Robin, P
    Lorain, S
    Le Villain, JP
    Troalen, F
    Trouche, D
    Harel-Bellan, A
    [J]. NATURE, 1998, 391 (6667) : 601 - 605
  • [23] Neuronal activity-dependent cell survival mediated by transcription factor MEF2
    Mao, ZX
    Bonni, A
    Xia, F
    Nadal-Vicens, M
    Greenberg, ME
    [J]. SCIENCE, 1999, 286 (5440) : 785 - 790
  • [24] HDAC4 deacetylase associates with and represses the MEF2 transcription factor
    Miska, EA
    Karlsson, C
    Langley, E
    Nielsen, SJ
    Pines, J
    Kouzarides, T
    [J]. EMBO JOURNAL, 1999, 18 (18) : 5099 - 5107
  • [25] The transcriptional coactivators p300 and CBP are histone acetyltransferases
    Ogryzko, VV
    Schiltz, RL
    Russanova, V
    Howard, BH
    Nakatani, Y
    [J]. CELL, 1996, 87 (05) : 953 - 959
  • [26] Molecular mechanisms of myogenic coactivation by p300: Direct interaction with the activation domain of MyoD and with the MADS box of MEF2C
    Sartorelli, V
    Huang, J
    Hamamori, Y
    Kedes, L
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (02) : 1010 - 1026
  • [27] MEF-2 function is modified by a novel co-repressor, MITR
    Sparrow, DB
    Miska, EA
    Langley, E
    Reynaud-Deonauth, S
    Kotecha, S
    Towers, N
    Spohr, G
    Kouzarides, T
    Mohun, TJ
    [J]. EMBO JOURNAL, 1999, 18 (18) : 5085 - 5098
  • [28] Cabin 1, a negative regulator for calcineurin signaling in T lymphocytes
    Sun, L
    Youn, HD
    Loh, C
    Stolow, M
    He, WW
    Liu, JO
    [J]. IMMUNITY, 1998, 8 (06) : 703 - 711
  • [29] A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p
    Taunton, J
    Hassig, CA
    Schreiber, SL
    [J]. SCIENCE, 1996, 272 (5260) : 408 - 411
  • [30] Chromatin deacetylation by an ATP-dependent nucleosome remodelling complex
    Tong, JK
    Hassig, CA
    Schnitzler, GR
    Kingston, RE
    Schreiber, SL
    [J]. NATURE, 1998, 395 (6705) : 917 - 921