The Alteration of Subtelomeric DNA Methylation in Aging-Related Diseases

The telomere is located at the end of the chromosome and consists of a non-coding, repetitive DNA sequence. As the cell divides, the length of telomere gradually decreases. A very short telomere can terminate mitosis, and thus telomere length becomes a hallmark of cellular aging. The 500 kb region o...

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Main Authors: Haochang Hu, Bin Li, Shiwei Duan
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-01-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fgene.2018.00697/full
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author Haochang Hu
Bin Li
Shiwei Duan
author_facet Haochang Hu
Bin Li
Shiwei Duan
author_sort Haochang Hu
collection DOAJ
description The telomere is located at the end of the chromosome and consists of a non-coding, repetitive DNA sequence. As the cell divides, the length of telomere gradually decreases. A very short telomere can terminate mitosis, and thus telomere length becomes a hallmark of cellular aging. The 500 kb region of each autosomal arm terminal is the so-called subtelomeric region. Both telomere and subtelomere have high-density DNA repeats. Telomeres do not contain genes or CpG sequences, while subtelomeres contain small amounts of genes and high-density CpG sequences, and DNA methylation often occurs in subtelomeres. Previous studies have shown that aberrant methylation of subtelomeric DNA exists in many diseases, and it has a certain effect on the regulation of telomere length. In this review, we focus on the correlation between subtelomeric DNA methylation and aging-related diseases. We also summarize the relationship between subtelomeric methylation and telomere length in different diseases.
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spelling doaj.art-f95f0bddea424238bf4edc66942fa9c92022-12-22T03:15:58ZengFrontiers Media S.A.Frontiers in Genetics1664-80212019-01-01910.3389/fgene.2018.00697421721The Alteration of Subtelomeric DNA Methylation in Aging-Related DiseasesHaochang HuBin LiShiwei DuanThe telomere is located at the end of the chromosome and consists of a non-coding, repetitive DNA sequence. As the cell divides, the length of telomere gradually decreases. A very short telomere can terminate mitosis, and thus telomere length becomes a hallmark of cellular aging. The 500 kb region of each autosomal arm terminal is the so-called subtelomeric region. Both telomere and subtelomere have high-density DNA repeats. Telomeres do not contain genes or CpG sequences, while subtelomeres contain small amounts of genes and high-density CpG sequences, and DNA methylation often occurs in subtelomeres. Previous studies have shown that aberrant methylation of subtelomeric DNA exists in many diseases, and it has a certain effect on the regulation of telomere length. In this review, we focus on the correlation between subtelomeric DNA methylation and aging-related diseases. We also summarize the relationship between subtelomeric methylation and telomere length in different diseases.https://www.frontiersin.org/article/10.3389/fgene.2018.00697/fullepigenetic modificationsubtelomeric DNA methylationtelomere lengthtelomeraseage-related disease
spellingShingle Haochang Hu
Bin Li
Shiwei Duan
The Alteration of Subtelomeric DNA Methylation in Aging-Related Diseases
Frontiers in Genetics
epigenetic modification
subtelomeric DNA methylation
telomere length
telomerase
age-related disease
title The Alteration of Subtelomeric DNA Methylation in Aging-Related Diseases
title_full The Alteration of Subtelomeric DNA Methylation in Aging-Related Diseases
title_fullStr The Alteration of Subtelomeric DNA Methylation in Aging-Related Diseases
title_full_unstemmed The Alteration of Subtelomeric DNA Methylation in Aging-Related Diseases
title_short The Alteration of Subtelomeric DNA Methylation in Aging-Related Diseases
title_sort alteration of subtelomeric dna methylation in aging related diseases
topic epigenetic modification
subtelomeric DNA methylation
telomere length
telomerase
age-related disease
url https://www.frontiersin.org/article/10.3389/fgene.2018.00697/full
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