CREB required for the stability of new and reactivated fear memories

被引:476
作者
Kida, S
Josselyn, SA
de Ortiz, SP
Kogan, JH
Chevere, I
Masushige, S
Silva, AJ
机构
[1] Univ Calif Los Angeles, Dept Neurobiol, Los Angeles, CA 90095 USA
[2] Tokyo Univ Agr, Fac Appl Biosci, Dept Biosci, SetagayaKu, Tokyo 1568502, Japan
[3] Univ Calif Los Angeles, Dept Psychol, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Dept Psychiat, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Brain Res Inst, Los Angeles, CA 90095 USA
[6] Univ Puerto Rico, Dept Biol, San Juan, PR 00931 USA
关键词
D O I
10.1038/nn819
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The cAMP-responsive element binding protein (CREB) family of transcription factors is thought to be critical in memory formation. To define the role of CREB in distinct memory processes, we derived transgenic mice with an inducible and reversible CREB repressor by fusing CREBS133A to a tamoxifen (TAM)-dependent mutant of an estrogen receptor ligand-binding domain (LBD). We found that CREB is crucial for the consolidation of long-term conditioned fear memories, but not for encoding, storage or retrieval of these memories. Our studies also showed that CREB is required for the stability of reactivated or retrieved conditioned fear memories. Although the transcriptional processes necessary for the stability of initial and reactivated memories differ, CREB is required for both. The findings presented here delineate the memory processes that require CREB and demonstrate the power of LBD-inducible transgenic systems in the study of complex cognitive processes.
引用
收藏
页码:348 / 355
页数:8
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