| Literature DB >> 33419039 |
Masamitsu Yamaguchi1,2, Kentaro Omori1, Satoshi Asada1, Hideki Yoshida1.
Abstract
Amyotrophic lateral sclerosis (ALS) is the third most common neurodegenerative disorder and is sometimes associated with frontotemporal dementia. Charcot-Marie-Tooth disease (CMT) is one of the most commonly inherited peripheral neuropathies causing the slow progression of sensory and distal muscle defects. Of note, the severity and progression of CMT symptoms markedly vary. The phenotypic heterogeneity of ALS and CMT suggests the existence of modifiers that determine disease characteristics. Epigenetic regulation of biological functions via gene expression without alterations in the DNA sequence may be an important factor. The methylation of DNA, noncoding RNA, and post-translational modification of histones are the major epigenetic mechanisms. Currently, Drosophila is emerging as a useful ALS and CMT model. In this review, we summarize recent studies linking ALS and CMT to epigenetic regulation with a strong emphasis on approaches using Drosophila models.Entities:
Keywords: Charcot–Marie–Tooth disease; Drosophila melanogaster; amyotrophic lateral sclerosis; epigenetics; genetic screening; histone modification enzyme; long noncoding RNA
Year: 2021 PMID: 33419039 DOI: 10.3390/ijms22020491
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923