Activity-Dependent Transport of the Transcriptional Coactivator CRTC1 from Synapse to Nucleus

被引:159
|
作者
Ch'ng, Toh Hean [1 ]
Uzgil, Besim [2 ]
Lin, Peter [3 ]
Avliyakulov, Nuraly K. [1 ]
O'Dell, Thomas J. [4 ]
Martin, Kelsey C. [1 ,5 ,6 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Interdept Program Neurosci, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Physiol, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA
[6] Univ Calif Los Angeles, David Geffen Sch Med, Integrated Ctr Learning & Memory, Los Angeles, CA 90095 USA
关键词
ELEMENT-BINDING PROTEIN; LONG-TERM POTENTIATION; SENSITIVE COINCIDENCE DETECTOR; MEDIATED GENE-EXPRESSION; MEMORY STORAGE; CREB; PLASTICITY; HIPPOCAMPUS; ACTIVATION; RECEPTOR;
D O I
10.1016/j.cell.2012.05.027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Long-lasting changes in synaptic efficacy, such as those underlying long-term memory, require transcription. Activity-dependent transport of synaptically localized transcriptional regulators provides a direct means of coupling synaptic stimulation with changes in transcription. The CREB-regulated transcriptional coactivator (CRTC1), which is required for long-term hippocampal plasticity, binds CREB to potently promote transcription. We show that CRTC1 localizes to synapses in silenced hippocampal neurons but translocates to the nucleus in response to localized synaptic stimulation. Regulated nuclear translocation occurs only in excitatory neurons and requires calcium influx and calcineurin activation. CRTC1 is controlled in a dual fashion with activity regulating CRTC1 nuclear translocation and cAMP modulating its persistence in the nucleus. Neuronal activity triggers a complex change in CRTC1 phosphorylation, suggesting that CRTC1 may link specific types of stimuli to specific changes in gene expression. Together, our results indicate that synapse-to-nuclear transport of CRTC1 dynamically informs the nucleus about synaptic activity.
引用
收藏
页码:207 / 221
页数:15
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