Characterization of Small RNAs in Aplysia Reveals a Role for miR-124 in Constraining Synaptic Plasticity through CREB

被引:357
作者
Rajasethupathy, Priyamvada [2 ,3 ]
Fiumara, Ferdinando [2 ,6 ]
Sheridan, Robert [7 ]
Betel, Doron [7 ]
Puthanveettil, Sathyanarayanan V. [2 ,3 ]
Russo, James J. [5 ]
Sander, Chris [7 ]
Tuschl, Thomas [1 ]
Kandel, Eric [2 ,3 ,4 ]
机构
[1] Rockefeller Univ, Howard Hughes Med Inst, Lab RNA Mol Biol, New York, NY 10065 USA
[2] Columbia Univ, Dept Neurosci, New York, NY 10032 USA
[3] Columbia Univ, Howard Hughes Med Inst, New York, NY 10032 USA
[4] Columbia Univ, Kavli Inst Brain Sci, New York, NY 10032 USA
[5] Columbia Univ, Columbia Genome Ctr, New York, NY 10032 USA
[6] Univ Turin, Dept Neurosci, I-10125 Turin, Italy
[7] Mem Sloan Kettering Canc Ctr, Computat & Syst Biol Ctr, New York, NY 10065 USA
关键词
LONG-TERM FACILITATION; POSTTRANSCRIPTIONAL REGULATION; PROTEIN-SYNTHESIS; FEEDBACK LOOP; MICRORNAS; EXPRESSION; EVOLUTION; NEURONS; GENES; CELL;
D O I
10.1016/j.neuron.2009.05.029
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Memory storage and memory-related synaptic plasticity rely on precise spatiotemporal regulation of gene expression. To explore the role of small regulatory RNAs in learning-related synaptic plasticity, we carried out massive parallel sequencing to profile the small RNAs of Aplysia californica. We identified 170 distinct miRNAs, 13 of which were novel and specific to Aplysia. Nine miRNAs were brain enriched, and several of these were rapidly downregulated by transient exposure to serotonin, a modulatory neurotransmitter released during learning. Further characterization of the brain-enriched miRNAs revealed that miR-124, the most abundant and well-conserved brain-specific miRNA, was exclusively present presynaptically in a sensory-motor synapse where it constrains serotonin-induced synaptic facilitation through regulation of the transcriptional factor CREB. We therefore present direct evidence that a modulatory neurotransmitter important for learning can regulate the levels of small RNAs and present a role for miR-124 in long-term plasticity of synapses in the mature nervous system.
引用
收藏
页码:803 / 817
页数:15
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[11]   Argonaute HITS-CLIP decodes microRNA-mRNA interaction maps [J].
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[13]   The widespread impact of mammalian microRNAs on mRNA repression and evolution [J].
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[14]   Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight? [J].
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[16]   Identification of microRNAs and other small regulatory RNAs using cDNA library sequencing [J].
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[17]   Ubiquitin C-terminal hydrolase is an immediate-early gene essential for long-term facilitation in Aplysia [J].
Hegde, AN ;
Inokuchi, K ;
Pei, WZ ;
Casadio, A ;
Ghirardi, M ;
Chain, DG ;
Martin, KC ;
Kandel, ER ;
Schwartz, JH .
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[18]   Lin28 Mediates the Terminal Uridylation of let-7 Precursor MicroRNA [J].
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[19]   Structure and mechanism of RNA ligase [J].
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Lima, CD ;
Shuman, S .
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[20]   Cross talk between ERK and PKA is required for Ca2+ stimulation of CREB-dependent transcription and ERK nuclear translocation [J].
Impey, S ;
Obrietan, K ;
Wong, ST ;
Poser, S ;
Yano, S ;
Wayman, G ;
Deloulme, JC ;
Chan, G ;
Storm, DR .
NEURON, 1998, 21 (04) :869-883