| Literature DB >> 27091986 |
Shari Orlanski1, Verena Labi2, Yitzhak Reizel1, Adam Spiro1, Michal Lichtenstein1, Rena Levin-Klein1, Sergei B Koralov3, Yael Skversky1, Klaus Rajewsky4, Howard Cedar1, Yehudit Bergman5.
Abstract
There is ample evidence that somatic cell differentiation during development is accompanied by extensive DNA demethylation of specific sites that vary between cell types. Although the mechanism of this process has not yet been elucidated, it is likely to involve the conversion of 5mC to 5hmC by Tet enzymes. We show that a Tet2/Tet3 conditional knockout at early stages of B-cell development largely prevents lineage-specific programmed demethylation events. This lack of demethylation affects the expression of nearby B-cell lineage genes by impairing enhancer activity, thus causing defects in B-cell differentiation and function. Thus, tissue-specific DNA demethylation appears to be necessary for proper somatic cell development in vivo.Entities:
Keywords: DMRs; Tet2/Tet3; chromatin; differentially methylated regions
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Year: 2016 PMID: 27091986 PMCID: PMC4983829 DOI: 10.1073/pnas.1604365113
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205