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| <dc:title>Cell Cycle</dc:title> | |
| <prism:volume>10</prism:volume> | |
| <prism:number>16</prism:number> | |
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| <foaf:surname>Guo</foaf:surname> | |
| <foaf:givenname>Junjie U.</foaf:givenname> | |
| </foaf:Person> | |
| </rdf:li> | |
| <rdf:li> | |
| <foaf:Person> | |
| <foaf:surname>Su</foaf:surname> | |
| <foaf:givenname>Yijing</foaf:givenname> | |
| </foaf:Person> | |
| </rdf:li> | |
| <rdf:li> | |
| <foaf:Person> | |
| <foaf:surname>Zhong</foaf:surname> | |
| <foaf:givenname>Chun</foaf:givenname> | |
| </foaf:Person> | |
| </rdf:li> | |
| <rdf:li> | |
| <foaf:Person> | |
| <foaf:surname>Ming</foaf:surname> | |
| <foaf:givenname>Guo-li</foaf:givenname> | |
| </foaf:Person> | |
| </rdf:li> | |
| <rdf:li> | |
| <foaf:Person> | |
| <foaf:surname>Song</foaf:surname> | |
| <foaf:givenname>Hongjun</foaf:givenname> | |
| </foaf:Person> | |
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| <link:link rdf:resource="#item_1512"/> | |
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| <z:AutomaticTag><rdf:value>Binding</rdf:value></z:AutomaticTag> | |
| </dc:subject> | |
| <dc:subject> | |
| <z:AutomaticTag><rdf:value>biology</rdf:value></z:AutomaticTag> | |
| </dc:subject> | |
| <dc:subject> | |
| <z:AutomaticTag><rdf:value>Bioscience</rdf:value></z:AutomaticTag> | |
| </dc:subject> | |
| <dc:subject> | |
| <z:AutomaticTag><rdf:value>Calcium</rdf:value></z:AutomaticTag> | |
| </dc:subject> | |
| <dc:subject> | |
| <z:AutomaticTag><rdf:value>cancer</rdf:value></z:AutomaticTag> | |
| </dc:subject> | |
| <dc:subject> | |
| <z:AutomaticTag><rdf:value>Cell</rdf:value></z:AutomaticTag> | |
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| <dc:subject> | |
| <z:AutomaticTag><rdf:value>Cycle</rdf:value></z:AutomaticTag> | |
| </dc:subject> | |
| <dc:subject> | |
| <z:AutomaticTag><rdf:value>Landes</rdf:value></z:AutomaticTag> | |
| </dc:subject> | |
| <dc:subject> | |
| <z:AutomaticTag><rdf:value>Organogenesis</rdf:value></z:AutomaticTag> | |
| </dc:subject> | |
| <dc:subject> | |
| <z:AutomaticTag><rdf:value>Proteins</rdf:value></z:AutomaticTag> | |
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| <dc:title>Emerging roles of TET proteins and 5-hydroxymethylcytosines in active DNA demethylation and beyond</dc:title> | |
| <dcterms:abstract>Cytosine methylation is the major epigenetic modification of metazoan DNA. Although there is strong evidence that active DNA demethylation occurs in animal cells, the molecular details of this process are unknown. The recent discovery of the TET protein family (TET1–3) 5-methylcytosine hydroxylases has provided a new entry point to reveal the identity of the long-sought DNA demethylase. Here, we review the recent progress in understanding the function of TET proteins and 5-hydroxymethylcytosine (5hmC) through various biochemical and genomic approaches, the current evidence for a role of 5hmC as an early intermediate in active DNA demethylation and the potential functions of TET proteins and 5hmC beyond active DNA demethylation. We also discuss how future studies can extend our knowledge of this novel epigenetic modification.</dcterms:abstract> | |
| <bib:pages>2662-2668</bib:pages> | |
| <dc:date>2011/08/15</dc:date> | |
| <dc:identifier> | |
| <dcterms:URI> | |
| <rdf:value>http://www.landesbioscience.com/journals/cc/article/17093/</rdf:value> | |
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| <dcterms:dateSubmitted>2012-06-20 20:34:25</dcterms:dateSubmitted> | |
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| <foaf:givenname>Junjie U.</foaf:givenname> | |
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| </rdf:li> | |
| <rdf:li> | |
| <foaf:Person> | |
| <foaf:surname>Su</foaf:surname> | |
| <foaf:givenname>Yijing</foaf:givenname> | |
| </foaf:Person> | |
| </rdf:li> | |
| <rdf:li> | |
| <foaf:Person> | |
| <foaf:surname>Zhong</foaf:surname> | |
| <foaf:givenname>Chun</foaf:givenname> | |
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| <rdf:li> | |
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| <foaf:surname>Ming</foaf:surname> | |
| <foaf:givenname>Guo-li</foaf:givenname> | |
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| <rdf:li> | |
| <foaf:Person> | |
| <foaf:surname>Song</foaf:surname> | |
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| <dc:title>Hydroxylation of 5-Methylcytosine by TET1 Promotes Active DNA Demethylation in the Adult Brain</dc:title> | |
| <dcterms:abstract>Summary | |
| Cytosine methylation is the major covalent modification of mammalian genomic DNA and plays important roles in transcriptional regulation. The molecular mechanism underlying the enzymatic removal of this epigenetic mark, however, remains elusive. Here, we show that 5-methylcytosine (5mC) hydroxylase TET1, by converting 5mCs to 5-hydroxymethylcytosines (5hmCs), promotes DNA demethylation in mammalian cells through a process that requires the base excision repair pathway. Though expression of the 12 known human DNA glycosylases individually did not enhance removal of 5hmCs in mammalian cells, demethylation of both exogenously introduced and endogenous 5hmCs is promoted by the AID (activation-induced deaminase)/APOBEC (apolipoprotein B mRNA-editing enzyme complex) family of cytidine deaminases. Furthermore, Tet1 and Apobec1 are involved in neuronal activity-induced, region-specific, active DNA demethylation and subsequent gene expression in the dentate gyrus of the adult mouse brain in vivo. Our study suggests a TET1-induced oxidation-deamination mechanism for active DNA demethylation in mammals.</dcterms:abstract> | |
| <bib:pages>423-434</bib:pages> | |
| <dc:date>April 29, 2011</dc:date> | |
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| </dc:identifier> | |
| <dcterms:dateSubmitted>2012-11-30 07:24:01</dcterms:dateSubmitted> | |
| <z:libraryCatalog>ScienceDirect</z:libraryCatalog> | |
| </bib:Article> | |
| <bib:Journal rdf:about="urn:issn:0092-8674"> | |
| <dc:title>Cell</dc:title> | |
| <prism:volume>145</prism:volume> | |
| <prism:number>3</prism:number> | |
| <dcterms:alternative>Cell</dcterms:alternative> | |
| <dc:identifier>DOI 10.1016/j.cell.2011.03.022</dc:identifier> | |
| <dc:identifier>ISSN 0092-8674</dc:identifier> | |
| </bib:Journal> | |
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