An evaluation of specificity in activity-dependent gene expression in neurons

被引:21
作者
Bradley, J
Finkbeiner, S [1 ]
机构
[1] Univ Calif San Francisco, Dept Neurol, Gladstone Inst Neurol Dis, San Francisco, CA 94103 USA
[2] Univ Calif San Francisco, Dept Physiol, Gladstone Inst Neurol Dis, San Francisco, CA 94103 USA
关键词
D O I
10.1016/S0301-0082(02)00047-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Activity-dependent synaptic modification must occur specifically to preserve the large information storage capacity of neurons. Since long-term changes in synaptic strength require gene expression and new protein synthesis we consider the role that gene expression plays in the specificity of synaptic modification. Ca2+ influx is essential for transducing synaptic activity into gene expression. Different temporal profiles of increased global Ca2+ and different types of Ca2+ channel have been demonstrated to produce different effects in the nucleus. It is possible therefore that synaptic activity may produce different programs of gene expression which may in turn control specific long-term changes in synaptic strength. We review recent data which suggest that the spatial properties of Ca2+ influx may provide a mechanism for the selective activation of molecules which signal to the nucleus. In particular, we describe data which suggests that Ca2+ channels may function in signal complexes at the synapse to propagate signals that contribute to distinct nuclear responses. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:469 / 477
页数:9
相关论文
共 62 条
[1]   REGULATION OF GENE-EXPRESSION IN HIPPOCAMPAL-NEURONS BY DISTINCT CALCIUM SIGNALING PATHWAYS [J].
BADING, H ;
GINTY, DD ;
GREENBERG, ME .
SCIENCE, 1993, 260 (5105) :181-186
[2]   Neuronal calcium signaling [J].
Berridge, MJ .
NEURON, 1998, 21 (01) :13-26
[3]   Protein targeting and calcium signaling microdomains in neuronal cells [J].
Blackstone, C ;
Sheng, M .
CELL CALCIUM, 1999, 26 (05) :181-192
[4]  
BRADLEY J, 2001, SOC NEUR ABSTR, V27
[5]   Physiological patterns of electrical stimulation can induce neuronal gene expression by activating N-type calcium channels [J].
Brosenitsch, TA ;
Katz, DM .
JOURNAL OF NEUROSCIENCE, 2001, 21 (08) :2571-2579
[6]   Gene regulation by patterned electrical activity during neural and skeletal muscle development [J].
Buonanno, A ;
Fields, RD .
CURRENT OPINION IN NEUROBIOLOGY, 1999, 9 (01) :110-120
[7]   CBP: A signal-regulated transcriptional coactivator controlled by nuclear calcium and CaM kinase IV [J].
Chawla, S ;
Hardingham, GE ;
Quinn, DR ;
Bading, H .
SCIENCE, 1998, 281 (5382) :1505-1509
[8]   A synaptic Ras-GTPase activating protein (p135 SynGAP) inhibited by CaM kinase II [J].
Chen, HJ ;
Rojas-Soto, M ;
Oguni, A ;
Kennedy, MB .
NEURON, 1998, 20 (05) :895-904
[9]   Hormone-induced secretory and nuclear translocation of calmodulin:: Oscillations of calmodulin concentration with the nucleus as an integrator [J].
Craske, H ;
Takeo, T ;
Gerasimenko, O ;
Vaillant, C ;
Török, K ;
Petersen, OH ;
Tepikin, AV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4426-4431
[10]  
Curtis J, 1999, J NEUROSCI RES, V58, P88, DOI 10.1002/(SICI)1097-4547(19991001)58:1<88::AID-JNR9>3.0.CO