Literature DB >> 32738421

Recent advancements in understanding the role of epigenetics in the auditory system.

Rahul Mittal1, Nicole Bencie1, George Liu1, Nicolas Eshraghi1, Eric Nisenbaum1, Susan H Blanton2, Denise Yan1, Jeenu Mittal1, Christine T Dinh1, Juan I Young3, Feng Gong4, Xue Zhong Liu5.   

Abstract

Sensorineural deafness in mammals is most commonly caused by damage to inner ear sensory epithelia, or hair cells, and can be attributed to genetic and environmental causes. After undergoing trauma, many non-mammalian organisms, including reptiles, birds, and zebrafish, are capable of regenerating damaged hair cells. Mammals, however, are not capable of regenerating damaged inner ear sensory epithelia, so that hair cell damage is permanent and can lead to hearing loss. The field of epigenetics, which is the study of various phenotypic changes caused by modification of genetic expression rather than alteration of DNA sequence, has seen numerous developments in uncovering biological mechanisms of gene expression and creating various medical treatments. However, there is a lack of information on the precise contribution of epigenetic modifications in the auditory system, specifically regarding their correlation with development of inner ear (cochlea) and consequent hearing impairment. Current studies have suggested that epigenetic modifications influence differentiation, development, and protection of auditory hair cells in cochlea, and can lead to hair cell degeneration. The objective of this article is to review the existing literature and discuss the advancements made in understanding epigenetic modifications of inner ear sensory epithelial cells. The analysis of the emerging epigenetic mechanisms related to inner ear sensory epithelial cells development, differentiation, protection, and regeneration will pave the way to develop novel therapeutic strategies for hearing loss.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Auditory system; Epigenetics; Hearing; Sensory epithelial cells

Mesh:

Year:  2020        PMID: 32738421      PMCID: PMC8168289          DOI: 10.1016/j.gene.2020.144996

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  153 in total

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Review 3.  Gap junctions and connexins in the inner ear: their roles in homeostasis and deafness.

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4.  Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss.

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Journal:  Eur Arch Otorhinolaryngol       Date:  2014-09-12       Impact factor: 2.503

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6.  Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss.

Authors:  Christopher J Klein; Maria-Victoria Botuyan; Yanhong Wu; Christopher J Ward; Garth A Nicholson; Simon Hammans; Kaori Hojo; Hiromitch Yamanishi; Adam R Karpf; Douglas C Wallace; Mariella Simon; Cecilie Lander; Lisa A Boardman; Julie M Cunningham; Glenn E Smith; William J Litchy; Benjamin Boes; Elizabeth J Atkinson; Sumit Middha; P James B Dyck; Joseph E Parisi; Georges Mer; David I Smith; Peter J Dyck
Journal:  Nat Genet       Date:  2011-05-01       Impact factor: 38.330

7.  A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population.

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8.  Epigenetic DNA Demethylation Causes Inner Ear Stem Cell Differentiation into Hair Cell-Like Cells.

Authors:  Yang Zhou; Zhengqing Hu
Journal:  Front Cell Neurosci       Date:  2016-08-03       Impact factor: 5.505

Review 9.  Writing, erasing and reading histone lysine methylations.

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10.  An integrated encyclopedia of DNA elements in the human genome.

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2.  Dnmt1 is required for the development of auditory organs via cell cycle arrest and Fgf signalling.

Authors:  Dongmei Tang; Shimei Zheng; Zhiwei Zheng; Chang Liu; Jiner Zhang; Renchun Yan; Cheng Wu; Na Zuo; Lijuan Wu; Hongfei Xu; Shaofeng Liu; Yingzi He
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