Spatial Memory Consolidation is Associated with Induction of Several Lysine-Acetyltransferase (Histone Acetyltransferase) Expression Levels and H2B/H4 Acetylation-Dependent Transcriptional Events in the Rat Hippocampus

被引:127
|
作者
Bousiges, Olivier [2 ]
de Vasconcelos, Anne Pereira [3 ]
Neidl, Romain
Cosquer, Brigitte [3 ]
Herbeaux, Karine [3 ]
Panteleeva, Irina
Loeffler, Jean-Philippe
Cassel, Jean-Christophe [3 ]
Boutillier, Anne-Laurence [1 ]
机构
[1] Univ Strasbourg, INSERM, UMRS692,U692, Lab Signalisat Mol & Neurodegenerescence,Fac Med, F-67085 Strasbourg, France
[2] Hop Univ Strasbourg, Serv Neurol, Strasbourg, France
[3] Univ Strasbourg, LINC FRE3289, Inst Fed Rech, GDR 2905,CNRS,IFR 37, F-67085 Strasbourg, France
关键词
hippocampus-dependent memory; CREB-binding protein CBP; histone acetyltransferase; H2B histone; Morris water maze; memory consolidation; CREB-BINDING-PROTEIN; LONG-TERM-MEMORY; RUBINSTEIN-TAYBI-SYNDROME; CHROMATIN-MODIFYING ENZYMES; MOUSE MODEL; ALZHEIMERS-DISEASE; DEACETYLASE INHIBITORS; SYNAPTIC PLASTICITY; COACTIVATOR CBP; GENE-EXPRESSION;
D O I
10.1038/npp.2010.117
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Numerous genetic studies have shown that the CREB-binding protein (CBP) is an essential component of long-term memory formation, through its histone acetyltransferase (HAT) function. E1A-binding protein p300 and p300/CBP-associated factor (PCAF) have also recently been involved in memory formation. By contrast, only a few studies have reported on acetylation modifications during memory formation, and it remains unclear as to how the system is regulated during this dynamic phase. We investigated acetylation-dependent events and the expression profiles of these HATs during a hippocampus-dependent task taxing spatial reference memory in the Morris water maze. We found a specific increase in H2B and H4 acetylation in the rat dorsal hippocampus, while spatial memory was being consolidated. This increase correlated with the degree of specific acetylated histones enrichment on some memory/plasticity-related gene promoters. Overall, a global increase in HAT activity was measured during this memory consolidation phase, together with a global increase of CBP, p300, and PCAF expression. Interestingly, these regulations were altered in a model of hippocampal denervation disrupting spatial memory consolidation, making it impossible for the hippocampus to recruit the CBP pathway (CBP regulation and acetylated-H2B-dependent transcription). CBP has long been thought to be present in limited concentrations in the cells. These results show, for the first time, that CBP, p300, and PCAF are dynamically modulated during the establishment of a spatial memory and are likely to contribute to the induction of a specific epigenetic tagging of the genome for hippocampus-dependent (spatial) memory consolidation. These findings suggest the use of HAT-activating molecules in new therapeutic strategies of pathological aging, Alzheimer's disease, and other neurodegenerative disorders. Neuropsychopharmacology (2010) 35, 2521-2537; doi:10.1038/npp.2010.117; published online 1 September 2010
引用
收藏
页码:2521 / 2537
页数:17
相关论文
共 8 条
  • [1] Spatial Memory Consolidation is Associated with Induction of Several Lysine-Acetyltransferase (Histone Acetyltransferase) Expression Levels and H2B/H4 Acetylation-Dependent Transcriptional Events in the Rat Hippocampus
    Olivier Bousiges
    Anne Pereira de Vasconcelos
    Romain Neidl
    Brigitte Cosquer
    Karine Herbeaux
    Irina Panteleeva
    Jean-Philippe Loeffler
    Jean-Christophe Cassel
    Anne-Laurence Boutillier
    Neuropsychopharmacology, 2010, 35 : 2521 - 2537
  • [2] MYST2 acetyltransferase expression and Histone H4 Lysine acetylation are suppressed in AML
    Sauer, Tim
    Arteaga, Maria Francisca
    Isken, Fabienne
    Rohde, Christian
    Hebestreit, Katja
    Mikesch, Jan-Henrik
    Stelljes, Matthias
    Cui, Chunhong
    Zhou, Fengbiao
    Goellner, Stefanie
    Baeumer, Nicole
    Koehler, Gabriele
    Krug, Utz
    Thiede, Christian
    Ehninger, Gerhard
    Edemir, Bayram
    Schlenke, Peter
    Berdel, Wolfgang E.
    Dugas, Martin
    Mueller-Tidow, Carsten
    EXPERIMENTAL HEMATOLOGY, 2015, 43 (09) : 794 - 802
  • [3] The Drosophila histone acetyltransferase Gcn5 and transcriptional adaptor Ada2a are involved in nucleosomal histone H4 acetylation
    Ciurciu, Anita
    Komonyi, Orban
    Pankotai, Tibor
    Boros, Imre M.
    MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (24) : 9413 - 9423
  • [4] RETRACTED: Detection of Histone Acetylation Levels in the Dorsal Hippocampus Reveals Early Tagging on Specific Residues of H2B and H4 Histones in Response to Learning (Retracted Article)
    Bousiges, Olivier
    Neidl, Romain
    Majchrzak, Monique
    Muller, Marc-Antoine
    Barbelivien, Alexandra
    de Vasconcelos, Anne Pereira
    Schneider, Anne
    Loeffler, Jean-Philippe
    Cassel, Jean-Christophe
    Boutillier, Anne-Laurence
    PLOS ONE, 2013, 8 (03):
  • [5] Distinct regions of the chicken p46 polypeptide are required for its in vitro interaction with histones H2B and H4 and histone acetyltransferase-1
    Ahmad, A
    Takami, Y
    Nakayama, T
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 279 (01) : 95 - 102
  • [6] RETRACTION: Detection of Histone Acetylation Levels in the Dorsal Hippocampus Reveals Early Tagging on Specific Residues of H2B and H4 Histones in Response to Learning (Retraction of Vol 8, art no E57816, 2013)
    Bousiges, O.
    Neidl, R.
    Majchrzak, M.
    Muller, M-A
    Barbelivien, A.
    de Vasconcelos, A. Pereira
    PLOS ONE, 2023, 18 (12):
  • [7] Induction by Fructose Force-Feeding of Histone H3 and H4 Acetylation at Their Lysine Residues around the Slc2a5 Gene and Its Expression in Mice
    Honma, Kazue
    Mochizuki, Kazuki
    Goda, Toshinao
    BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2013, 77 (11) : 2188 - 2191
  • [8] TATA element-binding protein is important to epidermal growth factor-dependent induction of H2B histone gene expression in primary hepatocytes from rat
    Lim, K
    Song, HJ
    Byun, SH
    Yun, KA
    Son, MY
    Park, JI
    Kweon, GR
    Yoon, WH
    Hwang, BD
    BIOCHEMISTRY AND MOLECULAR BIOLOGY INTERNATIONAL, 1998, 45 (03): : 575 - 582