Gene expression profiling in the amygdala: An approach to examine the molecular substrates of mammalian behavior

被引:18
作者
Dent, GW [1 ]
O'Dell, DM [1 ]
Eberwine, JH [1 ]
机构
[1] Univ Penn, Dept Pharmacol, Philadelphia, PA 19104 USA
关键词
antisense RNA; gene expression; microarray; amygdala;
D O I
10.1016/S0031-9384(01)00521-2
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
The molecular substrates of behavior have been difficult to assess because of the large number of messenger RNAs (mRNAs) expressed in a given brain region, the heterogeneous composition of the CNS, and the complexity of mammalian behavior. To gain insight into the molecular components of behavior requires an understanding of the anatomy associated with a specific behavior and the ability to examine multiple gene expression in discrete brain regions. Neuroanatomical and behavioral studies have demonstrated that the amygdaloid complex is an essential component of the neural pathways mediating behaviors, such as fear, anxiety, teaming, and memory. The amygdala is composed of several interconnected subnuclei and it is the modulation of information, as it flows through these subnuclei, that underlies amygdala function. To examine the molecular components of the amygdala, we have combined the antisense RNA (aRNA) amplification procedure with microarray technology. This experimental approach permits the simultaneous detection and quantification of numerous mRNAs in fixed tissue sections. Our initial experiment examines region-specific gene expression in naive mice in order to map the molecular relationship between the subregions of the amygdala. This report provides a general over-view of the techniques used to examine regional gene expression, suggests future experiments, and describes a theoretical framework for examining the molecular analysis of behavior. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:841 / 847
页数:7
相关论文
共 37 条
[1]   IMPAIRED RECOGNITION OF EMOTION IN FACIAL EXPRESSIONS FOLLOWING BILATERAL DAMAGE TO THE HUMAN AMYGDALA [J].
ADOLPHS, R ;
TRANEL, D ;
DAMASIO, H ;
DAMASIO, A .
NATURE, 1994, 372 (6507) :669-672
[2]   The amygdala theory of autism [J].
Baron-Cohen, S ;
Ring, HA ;
Bullmore, ET ;
Wheelwright, S ;
Ashwin, C ;
Williams, SCR .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2000, 24 (03) :355-364
[3]   HISTOANATOMIC OBSERVATIONS OF THE BRAIN IN EARLY INFANTILE-AUTISM [J].
BAUMAN, M ;
KEMPER, TL .
NEUROLOGY, 1985, 35 (06) :866-874
[4]   GENETIC DISSECTION OF BEHAVIOR [J].
BENZER, S .
SCIENTIFIC AMERICAN, 1973, 229 (06) :24-37
[6]   THE DISTRIBUTION OF NEURITIC PLAQUES AND ACETYLCHOLINESTERASE STAINING IN THE AMYGDALA IN ALZHEIMERS-DISEASE [J].
BRASHEAR, HR ;
GODEC, MS ;
CARLSEN, J .
NEUROLOGY, 1988, 38 (11) :1694-1699
[7]   INVOLVEMENT OF THE CENTRAL NUCLEUS AND BASOLATERAL COMPLEX OF THE AMYGDALA IN FEAR CONDITIONING MEASURED WITH FEAR-POTENTIATED STARTLE IN RATS TRAINED CONCURRENTLY WITH AUDITORY AND VISUAL CONDITIONED-STIMULI [J].
CAMPEAU, S ;
DAVIS, M .
JOURNAL OF NEUROSCIENCE, 1995, 15 (03) :2301-2311
[8]   Expression profiles of multiple genes in single neurons of Alzheimer's disease [J].
Chow, N ;
Cox, C ;
Callahan, LM ;
Weimer, JM ;
Guo, LR ;
Coleman, PD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (16) :9620-9625
[9]  
DREVETS WC, 1992, J NEUROSCI, V12, P3628
[10]   ANALYSIS OF GENE-EXPRESSION IN SINGLE LIVE NEURONS [J].
EBERWINE, J ;
YEH, H ;
MIYASHIRO, K ;
CAO, YX ;
NAIR, S ;
FINNELL, R ;
ZETTEL, M ;
COLEMAN, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) :3010-3014