4.8 Article

Global DNA Demethylation During Mouse Erythropoiesis in Vivo

Journal

SCIENCE
Volume 334, Issue 6057, Pages 799-802

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1207306

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Funding

  1. NIH/National Heart, Lung, and Blood Institute [R01 HL084168]
  2. American Cancer Society [RSG06-051-01]
  3. NIH CA [T32-130807]
  4. Diabetes Endocrinology Research Center [DK32520]
  5. Harvard Stem Cell Institute
  6. Pew Charitable Trust

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In the mammalian genome, 5'-CpG-3' dinucleotides are frequently methylated, correlating with transcriptional silencing. Genome-wide demethylation is thought to occur only twice during development, in primordial germ cells and in the pre-implantation embryo. These demethylation events are followed by de novo methylation, setting up a pattern inherited throughout development and modified only at tissue-specific loci. We studied DNA methylation in differentiating mouse erythroblasts in vivo by using genomic-scale reduced representation bisulfite sequencing (RRBS). Demethylation at the erythroid-specific beta-globin locus was coincident with global DNA demethylation at most genomic elements. Global demethylation was continuous throughout differentiation and required rapid DNA replication. Hence, DNA demethylation can occur globally during somatic cell differentiation, providing an experimental model for its study in development and disease.

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