Multiple chromatin modifications important for gene expression changes in cardiac hypertrophy

被引:4
作者
Bingham, A. J.
Ooi, L.
Wood, I. C. [1 ]
机构
[1] Univ Leeds, Inst Membrane & Syst Biol, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Leicester, Dept Cardiovasc Sci, Leicester LE3 9QP, Leics, England
关键词
atrial natriuretic peptide; brain natriuretic peptide; cardiac hypertrophy; chromatin; gene expression; repressor element 1-silencing transcription factor (REST);
D O I
10.1042/BST0341138
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
Cardiac hypertrophy is an increase in the size of cardiac myocytes to generate increased muscle mass, usually driven by increased workload for the heart. Although important during postnatal development and an adaptive response to physical exercise, excessive hypertrophy can result in heart failure. One characteristic of hypertrophy is the re-expression of genes that are normally only expressed during foetal heart development. Although the involvement of these changes in gene expression in hypertrophy has been known for some years, the mechanisms involved in this re-expression are only now being elucidated and the transcription factor REST (repressor element 1-silencing transcription factor) has been identified as an important repressor of hypertrophic gene expression.
引用
收藏
页码:1138 / 1140
页数:3
相关论文
共 16 条
  • [1] 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
  • [2] Distinct RE-1 silencing transcription factor-containing complexes interact with different target genes
    Belyaev, ND
    Wood, IC
    Bruce, AW
    Street, M
    Trinh, JB
    Buckley, NJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (01) : 556 - 561
  • [3] Genome-wide analysis of repressor element 1 silencing transcription factor/neuron-restrictive silencing factor (REST/NRSF) target genes
    Bruce, AW
    Donaldson, IJ
    Wood, IC
    Yerbury, SA
    Sadowski, MI
    Chapman, M
    Göttgens, B
    Buckley, NJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (28) : 10458 - 10463
  • [4] Calderone A, 2003, J NEUROSCI, V23, P2112
  • [5] Downregulated REST transcription factor is a switch enabling critical potassium channel expression and cell proliferation
    Cheong, A
    Bingham, AJ
    Li, J
    Kumar, B
    Sukumar, P
    Munsch, C
    Buckley, NJ
    Neylon, CB
    Porter, KE
    Beech, DJ
    Wood, IC
    [J]. MOLECULAR CELL, 2005, 20 (01) : 45 - 52
  • [6] Expression profiling reveals distinct sets of genes altered during induction and regression of cardiac hypertrophy
    Friddle, CJ
    Koga, T
    Rubin, EM
    Bristow, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) : 6745 - 6750
  • [7] 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
  • [8] Identification of the REST regulon reveals extensive transposable element-mediated binding site duplication
    Johnson, Rory
    Gamblin, Richard J.
    Ooi, Lezanne
    Bruce, Alexander W.
    Donaldson, Ian J.
    Westhead, David R.
    Wood, Ian C.
    Jackson, Richard M.
    Buckley, Noel J.
    [J]. NUCLEIC ACIDS RESEARCH, 2006, 34 (14) : 3862 - 3877
  • [9] The neuron-restrictive silencer element-neuron-restrictive silencer factor system regulates basal and endothelin 1-inducible atrial natriuretic peptide gene expression in ventricular myocytes
    Kuwahara, K
    Saito, Y
    Ogawa, E
    Takahashi, N
    Nakagawa, Y
    Naruse, Y
    Harada, M
    Hamanaka, I
    Izumi, T
    Miyamoto, Y
    Kishimoto, I
    Kawakami, R
    Nakanishi, M
    Mori, N
    Nakao, K
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (06) : 2085 - 2097
  • [10] NRSF regulates the fetal cardiac gene program and maintains normal cardiac structure and function
    Kuwahara, K
    Saito, Y
    Takano, M
    Arai, Y
    Yasuno, S
    Nakagawa, Y
    Takahashi, N
    Adachi, Y
    Takemura, G
    Horie, M
    Miyamoto, Y
    Morisaki, T
    Kuratomi, S
    Noma, A
    Fujiwara, H
    Yoshimasa, Y
    Kinoshita, H
    Kawakami, R
    Kishimoto, I
    Nakanishi, M
    Usami, S
    Saito, Y
    Harada, M
    Nakao, K
    [J]. EMBO JOURNAL, 2003, 22 (23) : 6310 - 6321