REST, a master transcriptional regulator in neurodegenerative disease

被引:159
|
作者
Hwang, Jee-Yeon [1 ]
Zukin, R. Suzanne [1 ]
机构
[1] Albert Einstein Coll Med, Rose F Kennedy Ctr, Dominick P Purpura Dept Neurosci, Room 610,1300 Morris Pk Ave, Bronx, NY 10461 USA
基金
美国国家卫生研究院;
关键词
SCF-BETA-TRCP; RESTRICTIVE SILENCING FACTOR; INDUCED NEURONAL DEATH; TARGET GENES; HIPPOCAMPAL-NEURONS; IN-VIVO; PSYCHIATRIC-DISORDERS; DEVELOPMENTAL SWITCH; HISTONE DEACETYLASE; MEMORY FORMATION;
D O I
10.1016/j.conb.2017.12.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The restrictive element-1 silencing transcription factor)/NRSF (neuron-restrictive silencing factor (NRSF) is a transcriptional repressor which acts via epigenetic remodeling to silence target genes. Emerging evidence indicates that REST is a master transcriptional regulator of neuron-specific genes not only in neurogenesis and neuronal differentiation, but also in differentiated neurons during the critical period in postnatal brain development, where it plays a role in fine-tuning of genes involved in synaptic plasticity, and in normal aging, where it promotes neuroprotection by repressing genes involved in oxidative stress and beta-amyloid toxicity. This review focuses on recent findings that dysregulation of REST and REST dependent epigenetic remodeling provide a central mechanism critical to the progressive neurodegeneration associated with neurologic disorders and diseases including global ischemia, stroke, epilepsy, Alzheimer's and Huntington's disease.
引用
收藏
页码:193 / 200
页数:8
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