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dc.contributor.authorShearstone, Jeffrey R.
dc.contributor.authorPop, Ramona
dc.contributor.authorBock, Christoph
dc.contributor.authorBoyle, Patrick
dc.contributor.authorMeissner, Alexander
dc.contributor.authorSocolovsky, Merav
dc.date2022-08-11T08:10:10.000
dc.date.accessioned2022-08-23T16:58:17Z
dc.date.available2022-08-23T16:58:17Z
dc.date.issued2011-11-11
dc.date.submitted2012-05-25
dc.identifier.citationScience. 2011 Nov 11;334(6057):799-802. DOI: 10.1126/science.1207306. <a href="http://dx.doi.org/10.1126/science.1207306">Link to article on publisher's website</a>
dc.identifier.issn1095-9203
dc.identifier.doi10.1126/science.1207306
dc.identifier.pmid22076376
dc.identifier.urihttp://hdl.handle.net/20.500.14038/43333
dc.description.abstractIn 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 β-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.
dc.language.isoen_US
dc.publisherAmerican Association for the Advancement of Science
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=22076376&dopt=Abstract">Link to article in PubMed</a>
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3230325/pdf/nihms338787.pdf
dc.subjectAnimals
dc.subjectCpG Islands
dc.subjectDNA Methylation
dc.subjectDNA Replication
dc.subjectDinucleoside Phosphates
dc.subjectEmbryo, Mammalian
dc.subjectErythroblasts
dc.subjectErythropoiesis
dc.subjectGene Expression Regulation, Developmental
dc.subjectGenome
dc.subjectLiver
dc.subjectLocus Control Region
dc.subjectLong Interspersed Nucleotide Elements
dc.subjectMice
dc.subjectS Phase
dc.subjectSequence Analysis, DNA
dc.subjectTranscription, Genetic
dc.subjectbeta-Globins
dc.subjectHematology
dc.subjectOncology
dc.subjectPediatrics
dc.titleGlobal DNA demethylation during mouse erythropoiesis in vivo
dc.typeJournal Article
dc.source.journaltitleScience
dc.source.volume334
dc.source.issue6057
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/peds_hematology/135
dc.identifier.contextkey2913925
html.description.abstract<p>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 β-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.</p>
dc.identifier.submissionpathpeds_hematology/135
dc.contributor.departmentDepartment of Cancer Biology
dc.contributor.departmentDepartment of Pediatrics
dc.source.pages799-802


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