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Neuroepigenetic mechanisms in disease

期刊

EPIGENETICS & CHROMATIN
卷 10, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s13072-017-0150-4

关键词

Neuroepigenetics; DNA methylation; Histone modification; Rett syndrome; Fragile X syndrome; Alzheimer's disease; MECP2; FMR1; LSD1/KDM1A

资金

  1. Emory CND [T32NS007480]
  2. Emory GMB [T32GM008490]
  3. National Institute of Neurological Disorders and Stroke [1R01NS087142]

向作者/读者索取更多资源

Epigenetics allows for the inheritance of information in cellular lineages during differentiation, independent of changes to the underlying genetic sequence. This raises the question of whether epigenetic mechanisms also function in post-mitotic neurons. During the long life of the neuron, fluctuations in gene expression allow the cell to pass through stages of differentiation, modulate synaptic activity in response to environmental cues, and fortify the cell through age-related neuroprotective pathways. Emerging evidence suggests that epigenetic mechanisms such as DNA methylation and histone modification permit these dynamic changes in gene expression throughout the life of a neuron. Accordingly, recent studies have revealed the vital importance of epigenetic players in the central nervous system and during neurodegeneration. Here, we provide a review of several of these recent findings, highlighting novel functions for epigenetics in the fields of Rett syndrome, Fragile X syndrome, and Alzheimer's disease research. Together, these discoveries underscore the vital importance of epigenetics in human neurological disorders.

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