RNA Protein Interaction in Neurons

被引:136
作者
Darnell, Robert B. [1 ]
机构
[1] Rockefeller Univ, Howard Hughes Med Inst, Dept Mol Neurooncol, New York, NY 10065 USA
来源
ANNUAL REVIEW OF NEUROSCIENCE, VOL 36 | 2013年 / 36卷
关键词
HITS-CLIP; Nova; Elavl; FMRP; microRNA; neuron-specific splicing factors; PRE-MESSENGER-RNA; TRACT-BINDING-PROTEIN; TRANSLATIONAL PROFILING APPROACH; ALTERNATIVE SPLICING EVENTS; LONG-TERM POTENTIATION; PANCREATIC BETA-CELLS; GENOME-WIDE ANALYSIS; FRAGILE-X; IN-VIVO; DROSOPHILA-MELANOGASTER;
D O I
10.1146/annurev-neuro-062912-114322
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Neurons have their own systems for regulating RNA. Several multigene families encode RNA binding proteins (RNABPs) that are uniquely expressed in neurons, including the well-known neuron-specific markers ELAV and NeuN and the disease antigen NOVA. New technologies have emerged in recent years to assess the function of these proteins in vivo, and the answers are yielding insights into how and why neurons may regulate RNA in special ways-to increase cellular complexity, to localize messenger RNA(mRNA) spatially, and to regulate their expression in response to synaptic stimuli. The functions of such restricted neuronal proteins are likely to be complemented by more widely expressed RNABPs that may themselves have developed specialized functions in neurons, including Argonaute/microRNAs (miRNAs). Here we review what is known about such RNABPs and explore the potential biologic and neurologic significance of neuronal RNA regulatory systems.
引用
收藏
页码:243 / 270
页数:28
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