Identification of genes expressed in the amygdala during the formation of fear memory

被引:64
作者
Stork, O [1 ]
Stork, S
Pape, HC
Obata, K
机构
[1] Natl Inst Physiol Sci, Neurochem Lab, Okazaki, Aichi 4448585, Japan
[2] Univ Magdeburg, Sch Med, Inst Physiol, D-39120 Magdeburg, Germany
关键词
D O I
10.1101/lm.39401
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In this study we describe changes of gene expression that occur in the basolateral complex of the mouse amygdala (BLA) during the formation of fear memory. Through the combination of a behavioral training scheme with polymerase chain reaction-based expression analysis (subtractive hybridization and virtual Northern analysis) we were able to identify various gene products that are increased in expression after Pavlovian fear conditioning and are of potential significance for neural plasticity and information storage in the amygdala. In particular, a key enzyme of monoamine metabolism, aldehyde reductase, and the protein sorting and ubiquitination factor Praja1, showed pronounced and learning-specific induction six hours after fear conditioning training. Aldehyde reductase and Praja1, including a novel alternatively spliced isoform termed Praja1a, were induced in the BLA depending on the emotional stimulus presented and showed different expression levels in response to associative conditioning, training stress, and experience of conditioned fear. Stress and fear were further found to induce various signal transduction factors (transthyretin, phosphodiesterase1, protein kinase inhibitor-alpha) and structural reorganization factors (e.g., E2-ubiquitin conjugating enzyme, neuroligin1, actin, UDP-galactose transporter) during training. Our results show that the formation of Pavlovian fear memory is associated with changes of gene expression in the BLA, which may contribute to neural plasticity and the processing of information about both conditioned and unconditioned fear stimuli.
引用
收藏
页码:209 / 219
页数:11
相关论文
共 43 条
[1]  
Baumgartner A, 1998, J NEUROCHEM, V71, P817
[2]  
BECK CHM, 1995, J NEUROSCI, V15, P709
[3]   DEFICIENT LONG-TERM-MEMORY IN MICE WITH A TARGETED MUTATION OF THE CAMP-RESPONSIVE ELEMENT-BINDING PROTEIN [J].
BOURTCHULADZE, R ;
FRENGUELLI, B ;
BLENDY, J ;
CIOFFI, D ;
SCHUTZ, G ;
SILVA, AJ .
CELL, 1994, 79 (01) :59-68
[4]   The basolateral amygdala complex is involved with, but is not necessary for, rapid acquisition of Pavlovian 'fear conditioning' [J].
Cahill, L ;
Vazdarjanova, A ;
Setlow, B .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2000, 12 (08) :3044-3050
[5]   INDUCTION OF THE C-FOS PROTOONCOGENE IN RAT AMYGDALA DURING UNCONDITIONED AND CONDITIONED FEAR [J].
CAMPEAU, S ;
HAYWARD, MD ;
HOPE, BT ;
ROSEN, JB ;
NESTLER, EJ ;
DAVIS, M .
BRAIN RESEARCH, 1991, 565 (02) :349-352
[6]   NEUROTRANSMISSION IN THE RAT AMYGDALA RELATED TO FEAR AND ANXIETY [J].
DAVIS, M ;
RAINNIE, D ;
CASSELL, M .
TRENDS IN NEUROSCIENCES, 1994, 17 (05) :208-214
[7]   Suppression subtractive hybridization: A method for generating differentially regulated or tissue-specific cDNA probes and libraries [J].
Diatchenko, L ;
Lau, YFC ;
Campbell, AP ;
Chenchik, A ;
Moqadam, F ;
Huang, B ;
Lukyanov, S ;
Lukyanov, K ;
Gurskaya, N ;
Sverdlov, ED ;
Siebert, PD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) :6025-6030
[8]   Mdm2 is a RING finger-dependent ubiquitin protein ligase for itself and p53 [J].
Fang, SY ;
Jensen, JP ;
Ludwig, RL ;
Vousden, KH ;
Weissman, AM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (12) :8945-8951
[9]   Synaptic tagging: implications for late maintenance of hippocampal long-term potentiation [J].
Frey, U ;
Morris, RGM .
TRENDS IN NEUROSCIENCES, 1998, 21 (05) :181-188
[10]   2 SENSITIVE PERIODS FOR THE AMNESIC EFFECT OF ANISOMYCIN [J].
GRECKSCH, G ;
MATTHIES, H .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1980, 12 (05) :663-665