RNA interference in hippocampus demonstrates opposing roles for CREB and PP1α in contextual and temporal long-term memory

被引:43
作者
Peters, M. [1 ,2 ]
Bletsch, M. [2 ]
Catapano, R. [2 ]
Zhang, X. [2 ]
Tully, T. [1 ,2 ]
Bourtchouladze, R. [2 ]
机构
[1] Dart Neurosci LLC, San Diego, CA 92121 USA
[2] Helicon Therapeut Inc, San Diego, CA USA
关键词
Contextual fear conditioning; contextual memory; CREB; hippocampus; long-term memory; PP1; RNA interference; siRNA; temporal memory; trace fear conditioning; ELEMENT-BINDING PROTEIN; NERVOUS-SYSTEM; TRANSCRIPTION FACTORS; SYNAPTIC PLASTICITY; DORSAL HIPPOCAMPUS; DENDRITIC SPINES; GENE-EXPRESSION; BRAIN; MICE; PHOSPHATASE-1;
D O I
10.1111/j.1601-183X.2009.00474.x
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
We injected small interfering RNAs (siRNAs) directly into the hippocampus of wild-type mice, knocking down expression of cyclic AMP responsive element-binding protein (CREB) and disrupting long-term, but not short-term, memory after both contextual and trace fear conditioning. In contrast, similar knockdown of siRNA for protein phosphatase 1 (PP1) was sufficient to enhance contextual and temporal memory formation, thereby demonstrating with such a gain-of-function effect a lack of any general deleterious effect for this method of RNAi-mediated gene knockdown. Our findings clearly confirm that contextual memory formation involves CREB and PP1 as positive and negative regulators, respectively, and show for the first time that temporal memory formation shares this mechanism. More generally, we establish that direct injection of siRNA into identified adult brain regions yields specific gene knockdowns, which can be used to validate in vivo candidate genes involved in behavioral plasticity.
引用
收藏
页码:320 / 329
页数:10
相关论文
共 50 条
[1]   Retraction of synapses and dendritic spines induced by off-target effects of RNA interference [J].
Alvarez, Veronica A. ;
Ridenour, Dennis A. ;
Sabatini, Bernardo L. .
JOURNAL OF NEUROSCIENCE, 2006, 26 (30) :7820-7825
[2]  
Anagnostaras SG, 2001, HIPPOCAMPUS, V11, P8
[3]   Hippocampal CRE-mediated gene expression is required for contextual memory formation [J].
Athos, J ;
Impey, S ;
Pineda, VV ;
Chen, X ;
Storm, DR .
NATURE NEUROSCIENCE, 2002, 5 (11) :1119-1120
[4]  
Balschun D, 2003, J NEUROSCI, V23, P6304
[5]   CREB phosphorylation and dephosphorylation: A Ca2(+)- and stimulus duration-dependent switch for hippocampal gene expression [J].
Bito, H ;
Deisseroth, K ;
Tsien, RW .
CELL, 1996, 87 (07) :1203-1214
[6]   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
[7]  
Büchel C, 1999, J NEUROSCI, V19, P10869
[8]   Classical conditioning and brain systems: The role of awareness [J].
Clark, RE ;
Squire, LR .
SCIENCE, 1998, 280 (5360) :77-81
[9]   RNA interference: A tool for querying nervous system function and an emerging therapy [J].
Davidson, Beverly L. ;
Boudreau, Ryan L. .
NEURON, 2007, 53 (06) :781-788
[10]   siRNAs: Applications in functional genomics and potential as therapeutics [J].
Dorsett, Y ;
Tuschl, T .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (04) :318-329