2017
DOI: 10.1186/s12867-016-0078-4
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Heterogeneous pattern of DNA methylation in developmentally important genes correlates with its chromatin conformation

Abstract: BackgroundDNA methylation is a major epigenetic modification, playing a crucial role in the development and differentiation of higher organisms. DNA methylation is also known to regulate transcription by gene repression. Various developmental genes such as c-mos, HoxB5, Sox11, and Sry show tissue-specific gene expression that was shown to be regulated by promoter DNA methylation. The aim of the present study is to investigate the establishment of chromatin marks (active or repressive) in relation to heterogene… Show more

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Cited by 12 publications
(3 citation statements)
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“…HR is a strand invasion mechanism that occurs during the late S to G2 phase of the cell cycle and is known to be unerring as it uses the presence of a homologous chromosome or sister chromatid as a template for the repair ( Figure 2A ) ( Essers et al, 2000 ). Human single stranded DNA binding protein 1 (hSSB1) has shown to be an essential protein to signal for DNA DSB repair through HR by recruiting the MRN (Mre11/Rad50/NBS1) complex to the lesion site ( Lawson et al, 2020 ; El-Kamand et al, 2020 ; Ashton et al, 2017 ; Croft et al, 2017 ; Touma et al, 2016 ; Paquet et al, 2016 ; Richard et al, 2011a ; Richard et al, 2011b ; Richard et al 2008 ). The MRN complex is responsible for activating the ATM kinase activity and binding the DNA ends at the break site ( D’Amours and Jackson 2002 ).…”
Section: Cancer Dna Damage and Epigenetic Changesmentioning
confidence: 99%
“…HR is a strand invasion mechanism that occurs during the late S to G2 phase of the cell cycle and is known to be unerring as it uses the presence of a homologous chromosome or sister chromatid as a template for the repair ( Figure 2A ) ( Essers et al, 2000 ). Human single stranded DNA binding protein 1 (hSSB1) has shown to be an essential protein to signal for DNA DSB repair through HR by recruiting the MRN (Mre11/Rad50/NBS1) complex to the lesion site ( Lawson et al, 2020 ; El-Kamand et al, 2020 ; Ashton et al, 2017 ; Croft et al, 2017 ; Touma et al, 2016 ; Paquet et al, 2016 ; Richard et al, 2011a ; Richard et al, 2011b ; Richard et al 2008 ). The MRN complex is responsible for activating the ATM kinase activity and binding the DNA ends at the break site ( D’Amours and Jackson 2002 ).…”
Section: Cancer Dna Damage and Epigenetic Changesmentioning
confidence: 99%
“…DNA methylation, the adding a methyl group to the DNA nucleotide cytosine, is the most studied epigenetic mark [61]. A strictly regulated pattern of DNA methylation is essential for normal in cellular differentiation in higher organisms and plays a vital role throughout life in the regulation and transcription of tissue-specific genes [62]. Research into DNA methylation erasure gained momentum a few years ago when 5-hmC an oxidation product of 5-mC was discovered and further oxidation steps would modify 5-hmC first to 5-fC and 5-caC.…”
Section: Figure2mentioning
confidence: 99%
“…Consistent with this observation, a separate study found that the Sry promoter has low levels of H3K9me3 and is enriched for the active H3K4me3 modification in E12.5 mouse testes. In contrast, adult testes have high H3K9me3 and low H3K4me3 enrichment, suggesting that the Sry locus regains H3K9me3 after it is silenced, and that this mark maintains long-term repression of Sry throughout adulthood in mice (Sinha et al, 2017). Recently, sex-reversal of Jmjd1a -deficient micewas rescued by disrupting the GLP/G9a H3K9 methyltransferase complex, pointing towards this complex as the one that catalyzes H3K9me2 at the Sry locus (Fig.…”
Section: Epigenetic Regulation Of the Primary Switchmentioning
confidence: 99%