HDAC signaling in neuronal development and axon regeneration

被引:97
作者
Cho, Yongcheol [1 ]
Cavalli, Valeria [1 ]
机构
[1] Washington Univ, Sch Med, Dept Anat & Neurobiol, St Louis, MO 63110 USA
关键词
HISTONE DEACETYLASE FAMILY; SPINAL-CORD-INJURY; GROWTH CONE; EPIGENETIC REGULATION; MEMORY FORMATION; GENE-EXPRESSION; NERVOUS-SYSTEM; NUCLEAR EXPORT; CELL-MIGRATION; STEM-CELLS;
D O I
10.1016/j.conb.2014.03.008
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The development and repair of the nervous system requires the coordinated expression of a large number of specific genes. Epigenetic modifications of histones represent an essential principle by which neurons regulate transcriptional responses and adapt to environmental cues. The post-translational modification of histones by chromatin-modifying enzymes histone acetyltransferases (HATs) and histone deacetylases (HDACs) shapes chromatin to adjust transcriptional profiles during neuronal development. Recent observations also point to a critical role for histone acetylation and deacetylation in the response of neurons to injury. While HDACs are mostly known to attenuate transcription through their deacetylase activity and their interaction with co-repressors, these enzymes are also found in the cytoplasm where they display transcription-independent activities by regulating the function of diverse proteins. Here we discuss recent studies that go beyond the traditional use of HDAC inhibitors and have begun to dissect the roles of individual HDAC isoforms in neuronal development and repair after injury.
引用
收藏
页码:118 / 126
页数:9
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