Cytoplasmic RNA-Binding Proteins and the Control of Complex Brain Function

被引:89
作者
Darnell, Jennifer C. [1 ]
Richter, Joel D. [2 ]
机构
[1] Rockefeller Univ, Dept Mol Neurooncol, New York, NY 10065 USA
[2] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
来源
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY | 2012年 / 4卷 / 08期
关键词
MENTAL-RETARDATION PROTEIN; MESSENGER-RIBONUCLEOPROTEIN COMPLEXES; REGULATES DENDRITE MORPHOGENESIS; CAP-DEPENDENT TRANSLATION; POLYADENYLATION ELEMENT; SYNAPTIC PLASTICITY; POSTTRANSCRIPTIONAL REGULATION; NEURONAL DEVELOPMENT; CROSS-LINKING; GRANULE CELLS;
D O I
10.1101/cshperspect.a012344
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The formation and maintenance of neural circuits in the mammal central nervous system (CNS) require the coordinated expression of genes not just at the transcriptional level, but at the translational level as well. Recent evidence shows that regulated messenger RNA (mRNA) translation is necessary for certain forms of synaptic plasticity, the cellular basis of learning and memory. In addition, regulated translation helps guide axonal growth cones to their targets on other neurons or at the neuromuscular junction. Several neurologic syndromes have been correlated with and indeed may be caused by aberrant translation; one important example is the fragile X mental retardation syndrome. Although translation in the CNS is regulated by multiple mechanisms and factors, we focus this review on regulatory mRNA-binding proteins with particular emphasis on fragile X mental retardation protein (FMRP) and cytoplasmic polyadenylation element binding (CPEB) because they have been shown to be at the nexus of translational control and brain function in health and disease.
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页数:17
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