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Department of Brain Sciences
Laboratory of Neurodegenerative Diseases and Aging
1. Journal Articles
Epigenetic Changes in Neurodegenerative Diseases
Kwon, Min Jee
;
Kim, Sunhong
;
Han, Myeong Hoon
;
Lee, Sung Bae
Department of Brain Sciences
Laboratory of Neurodegenerative Diseases and Aging
1. Journal Articles
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Title
Epigenetic Changes in Neurodegenerative Diseases
DGIST Authors
Lee, Sung Bae
Issued Date
2016-11
Citation
Kwon, Min Jee. (2016-11). Epigenetic Changes in Neurodegenerative Diseases. doi: 10.14348/molcells.2016.0233
Type
Article
Article Type
Review
Author Keywords
epigenetic changes
;
histone
;
neurodegenerative diseases
;
post-translational modifications
Keywords
LONG-TERM-MEMORY
;
CREB-BINDING-PROTEIN
;
HISTONE DEACETYLASE INHIBITOR
;
TRANSGENIC MOUSE MODEL
;
ALZHEIMERS-DISEASE
;
HUNTINGTONS-DISEASE
;
MUTANT HUNTINGTIN
;
DNA METHYLATION
;
AXONAL-TRANSPORT
;
TRUNCATED FORM
ISSN
1016-8478
Abstract
Afflicted neurons in various neurodegenerative diseases generally display diverse and complex pathological features before catastrophic occurrence of massive neuronal loss at the late stages of the diseases. This complex nature of neuronal pathophysiology inevitably implicates systemwide changes in basic cellular activities such as transcriptional controls and signal cascades, and so on, as a cause. Recently, as one of these systemwide cellular changes associated with neurodegenerative diseases, epigenetic changes caused by protein toxicity have begun to be highlighted. Notably, recent advances in related techniques including next-generation sequencing (NGS) and mass spectrometry enable us to monitor changes in the post-translational modifications (PTMs) of histone proteins and to link these changes in histone PTMs to the specific transcriptional changes. Indeed, epigenetic alterations and consequent changes in neuronal transcriptome are now begun to be extensively studied in neurodegenerative diseases including Alzheimer’s disease (AD). In this review, we will discuss details of our current understandings on epigenetic changes associated with two representative neurodegenerative diseases [AD and polyglutamine (polyQ) diseases] and further discuss possible future development of pharmaceutical treatment of the diseases through modulating these epigenetic changes. © The Korean Society for Molecular and Cellular Biology. All rights reserved.
URI
http://hdl.handle.net/20.500.11750/2124
DOI
10.14348/molcells.2016.0233
Publisher
Korean Society for Molecular and Cellular Biology
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