Proteins in DNA methylation and their role in neural stem cell proliferation and differentiation

Abstract Background Epigenetic modifications, namely non-coding RNAs, DNA methylation, and histone modifications such as methylation, phosphorylation, acetylation, ubiquitylation, and sumoylation play a significant role in brain development. DNA methyltransferases, methyl-CpG binding proteins, and t...

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Main Authors: Jiaqi Sun, Junzheng Yang, Xiaoli Miao, Horace H. Loh, Duanqing Pei, Hui Zheng
Format: Article
Language:English
Published: SpringerOpen 2021-03-01
Series:Cell Regeneration
Subjects:
Online Access:https://doi.org/10.1186/s13619-020-00070-4
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author Jiaqi Sun
Junzheng Yang
Xiaoli Miao
Horace H. Loh
Duanqing Pei
Hui Zheng
author_facet Jiaqi Sun
Junzheng Yang
Xiaoli Miao
Horace H. Loh
Duanqing Pei
Hui Zheng
author_sort Jiaqi Sun
collection DOAJ
description Abstract Background Epigenetic modifications, namely non-coding RNAs, DNA methylation, and histone modifications such as methylation, phosphorylation, acetylation, ubiquitylation, and sumoylation play a significant role in brain development. DNA methyltransferases, methyl-CpG binding proteins, and ten-eleven translocation proteins facilitate the maintenance, interpretation, and removal of DNA methylation, respectively. Different forms of methylation, including 5-methylcytosine, 5-hydroxymethylcytosine, and other oxidized forms, have been detected by recently developed sequencing technologies. Emerging evidence suggests that the diversity of DNA methylation patterns in the brain plays a key role in fine-tuning and coordinating gene expression in the development, plasticity, and disorders of the mammalian central nervous system. Neural stem cells (NSCs), originating from the neuroepithelium, generate neurons and glial cells in the central nervous system and contribute to brain plasticity in the adult mammalian brain. Main body Here, we summarized recent research in proteins responsible for the establishment, maintenance, interpretation, and removal of DNA methylation and those involved in the regulation of the proliferation and differentiation of NSCs. In addition, we discussed the interactions of chemicals with epigenetic pathways to regulate NSCs as well as the connections between proteins involved in DNA methylation and human diseases. Conclusion Understanding the interplay between DNA methylation and NSCs in a broad biological context can facilitate the related studies and reduce potential misunderstanding.
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spelling doaj.art-3905335db51a42579615401574ef710a2022-12-21T18:09:43ZengSpringerOpenCell Regeneration2045-97692021-03-0110111210.1186/s13619-020-00070-4Proteins in DNA methylation and their role in neural stem cell proliferation and differentiationJiaqi Sun0Junzheng Yang1Xiaoli Miao2Horace H. Loh3Duanqing Pei4Hui Zheng5Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory)Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory)Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory)Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory)Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory)Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory)Abstract Background Epigenetic modifications, namely non-coding RNAs, DNA methylation, and histone modifications such as methylation, phosphorylation, acetylation, ubiquitylation, and sumoylation play a significant role in brain development. DNA methyltransferases, methyl-CpG binding proteins, and ten-eleven translocation proteins facilitate the maintenance, interpretation, and removal of DNA methylation, respectively. Different forms of methylation, including 5-methylcytosine, 5-hydroxymethylcytosine, and other oxidized forms, have been detected by recently developed sequencing technologies. Emerging evidence suggests that the diversity of DNA methylation patterns in the brain plays a key role in fine-tuning and coordinating gene expression in the development, plasticity, and disorders of the mammalian central nervous system. Neural stem cells (NSCs), originating from the neuroepithelium, generate neurons and glial cells in the central nervous system and contribute to brain plasticity in the adult mammalian brain. Main body Here, we summarized recent research in proteins responsible for the establishment, maintenance, interpretation, and removal of DNA methylation and those involved in the regulation of the proliferation and differentiation of NSCs. In addition, we discussed the interactions of chemicals with epigenetic pathways to regulate NSCs as well as the connections between proteins involved in DNA methylation and human diseases. Conclusion Understanding the interplay between DNA methylation and NSCs in a broad biological context can facilitate the related studies and reduce potential misunderstanding.https://doi.org/10.1186/s13619-020-00070-4DNA methylationNeural stem cellsDNA methyltransferasesMethyl-CpG binding proteinsTen-eleven translocationsVitamin C
spellingShingle Jiaqi Sun
Junzheng Yang
Xiaoli Miao
Horace H. Loh
Duanqing Pei
Hui Zheng
Proteins in DNA methylation and their role in neural stem cell proliferation and differentiation
Cell Regeneration
DNA methylation
Neural stem cells
DNA methyltransferases
Methyl-CpG binding proteins
Ten-eleven translocations
Vitamin C
title Proteins in DNA methylation and their role in neural stem cell proliferation and differentiation
title_full Proteins in DNA methylation and their role in neural stem cell proliferation and differentiation
title_fullStr Proteins in DNA methylation and their role in neural stem cell proliferation and differentiation
title_full_unstemmed Proteins in DNA methylation and their role in neural stem cell proliferation and differentiation
title_short Proteins in DNA methylation and their role in neural stem cell proliferation and differentiation
title_sort proteins in dna methylation and their role in neural stem cell proliferation and differentiation
topic DNA methylation
Neural stem cells
DNA methyltransferases
Methyl-CpG binding proteins
Ten-eleven translocations
Vitamin C
url https://doi.org/10.1186/s13619-020-00070-4
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