Release of hypoacetylated and trimethylated histone H4 is an epigenetic marker of early apoptosis

被引:31
作者
Boix-Chornet, M
Fraga, MF
Villar-Garea, A
Caballero, R
Espada, J
Nuñez, A
Casado, J
Largo, C
Casal, JI
Cigudosa, JC
Franco, L
Esteller, M
Ballestar, E
机构
[1] Spanish Natl Canc Ctr, Canc Epigenet Lab, Mol Pathol Programme, Madrid 28029, Spain
[2] Spanish Natl Canc Ctr, Prot Technol Unit, Biotechnol Programme, Madrid 28029, Spain
[3] Spanish Natl Canc Ctr, Human Canc Genet Programme, Mol Cytogenet Grp, Madrid 28029, Spain
[4] Univ Salamanca, Canc Res Ctr, Lab 14, Salamanca 37007, Spain
[5] Univ Valencia, Dept Biochem & Mol Biol, Valencia 46100, Spain
关键词
D O I
10.1074/jbc.M601136200
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
Nuclear events such as chromatin condensation, DNAcleavage at internucleosomal sites, and histone release from chromatin are recognized as hallmarks of apoptosis. However, there is no complete understanding of the molecular events underlying these changes. It is likely that epigenetic changes such as DNA methylation and histone modifications that are involved in chromatin dynamics and structure are also involved in the nuclear events described. In this report we have shown that apoptosis is associated with global DNA hypomethylation and histone deacetylation events in leukemia cells. Most importantly, we have observed a particular epigenetic signature for early apoptosis defined by a release of hypoacetylated and trimethylated histone H4 and internucleosomal fragmented DNA that is hypermethylated and originates from perinuclear heterochromatin. These findings provide one of the first links between apoptotic nuclear events and epigenetic markers.
引用
收藏
页码:13540 / 13547
页数:8
相关论文
共 56 条
  • [1] Histone H2B phosphorylation in mammalian apoptotic cells - An association with DNA fragmentation
    Ajiro, K
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (01) : 439 - 443
  • [2] Allera C, 1997, J BIOL CHEM, V272, P10817
  • [3] ARENDS MJ, 1990, AM J PATHOL, V136, P593
  • [4] Core histones are glutaminyl substrates for tissue transglutaminase
    Ballestar, E
    Abad, C
    Franco, L
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (31) : 18817 - 18824
  • [5] Bonaldi T, 2004, METHOD ENZYMOL, V377, P111
  • [6] DNA METHYLATION AND GENE ACTIVITY
    CEDAR, H
    [J]. CELL, 1988, 53 (01) : 3 - 4
  • [7] Characterization of nonrandom chromosomal gains and losses in multiple myeloma by comparative genomic hybridization
    Cigudosa, JC
    Rao, PH
    Calasanz, MJ
    Odero, MD
    Michaeli, J
    Jhanwar, SC
    Chaganti, RSK
    [J]. BLOOD, 1998, 91 (08) : 3007 - 3010
  • [8] Nuclear compartments and gene regulation
    Cockell, M
    Gasser, SM
    [J]. CURRENT OPINION IN GENETICS & DEVELOPMENT, 1999, 9 (02) : 199 - 205
  • [9] Emerging connections between DNA methylation and histone acetylation
    Dobosy, JR
    Selker, EU
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2001, 58 (5-6) : 721 - 727
  • [10] DNA methylation in cancer: too much, but also too little
    Ehrlich, M
    [J]. ONCOGENE, 2002, 21 (35) : 5400 - 5413