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Open AccessJournal ArticleDOI

The Nuclear DNA Base 5-Hydroxymethylcytosine Is Present in Purkinje Neurons and the Brain

Skirmantas Kriaucionis, +1 more
- 15 May 2009 - 
- Vol. 324, Iss: 5929, pp 929-930
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TLDR
It is shown that, as well as 5mC in mammalian genomes, there are also significant amounts of 5-hydroxymethylcytosine (5hmC) in DNA of Purkinje neurons, which have large nuclei with apparently very little heterochromatin.
Abstract
Despite the importance of epigenetic regulation in neurological disorders, little is known about neuronal chromatin. Cerebellar Purkinje neurons have large and euchromatic nuclei, whereas granule cell nuclei are small and have a more typical heterochromatin distribution. While comparing the abundance of 5-methylcytosine in Purkinje and granule cell nuclei, we detected the presence of an unusual DNA nucleotide. Using thin-layer chromatography, high-pressure liquid chromatography, and mass spectrometry, we identified the nucleotide as 5-hydroxymethyl-2′-deoxycytidine (hmdC). hmdC constitutes 0.6% of total nucleotides in Purkinje cells, 0.2% in granule cells, and is not present in cancer cell lines. hmdC is a constituent of nuclear DNA that is highly abundant in the brain, suggesting a role in epigenetic control of neuronal function.

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Establishing, maintaining and modifying DNA methylation patterns in plants and animals

TL;DR: Drawing on insights from both plants and animals should deepen the understanding of the regulation and biological significance of DNA methylation.
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Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine

TL;DR: This study raises the possibility that DNA demethylation may occur through Tet-catalyzed oxidation followed by decarboxylation, and identifies two previously unknown cytosine derivatives in genomic DNA as the products of Tet proteins.
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Cancer epigenetics: from mechanism to therapy.

TL;DR: The basic principles behind DNA methylation, histone modification, nucleosome remodeling, and RNA-mediated targeting are presented and the evidence suggesting that their misregulation can culminate in cancer is highlighted.
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A decade of exploring the cancer epigenome — biological and translational implications

TL;DR: Next-generation sequencing is providing a window for visualizing the human epigenome and how it is altered in cancer, including linking epigenetic abnormalities to mutations in genes that control DNA methylation, the packaging and the function of DNA in chromatin, and metabolism.
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Epigenetic modifications and human disease

TL;DR: A comprehensive understanding of epigenetic mechanisms, their interactions and alterations in health and disease, has become a priority in biomedical research.
References
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Journal ArticleDOI

A Translational Profiling Approach for the Molecular Characterization of CNS Cell Types

TL;DR: This genetically targeted translating ribosome affinity purification (TRAP) methodology is a generalizable method useful for the identification of molecular changes in any genetically defined cell type in response to genetic alterations, disease, or pharmacological perturbations.
Journal ArticleDOI

Application of a Translational Profiling Approach for the Comparative Analysis of CNS Cell Types

TL;DR: In this article, translational profiles for 24 central nervous system (CNS) cell populations and identified known cell-specific and enriched transcripts for each population were presented. But, the translational profile for each cell population was not used in whole-tissue microarray studies.
Journal ArticleDOI

Oxidative damage to methyl-CpG sequences inhibits the binding of the methyl-CpG binding domain (MBD) of methyl-CpG binding protein 2 (MeCP2)

TL;DR: Oxidative damage to DNA could result in heritable, epigenetic changes in chromatin organization, and oxidation of either a single guanine to 8-oxoG or of a single 5mC to HmC, significantly inhibits binding of the MBD to the oligonucleotide duplex, reducing the binding affinity.
Journal ArticleDOI

The Colorful History of Active DNA Demethylation

TL;DR: Two recent reports in Nature now claim that the demethylation process is initiated by the same enzymes that establish the methylation mark, the DNA methyltransferases DNMT3A andDNMT3B.
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