Document Type
Article
Publication Date
4-23-2007
Publication Title
Molecular and Cellular Biology
Department
Geisel School of Medicine
Abstract
There is little evidence addressing the role of CpG methylation in transcriptional control of genes that do not contain CpG islands. This is reflected in the ongoing debate about whether CpG methylation merely suppresses retroelements or if it also plays a role in developmental and tissue-specific gene regulation. The genes of the β-globin locus are an important model of mammalian developmental gene regulation and do not contain CpG islands. We have analyzed the methylation status of regions in the murine β-like globin locus in uncultured primitive and definitive erythroblasts and other cultured primary and transformed cell types. A large (∼20-kb) domain is hypomethylated only in primitive erythroid cells; it extends from the region just past the locus control region to before β-major and encompasses the embryonic genes Ey, βh1, and βh0. Even retrotransposons in this region are hypomethylated in primitive erythroid cells. The existence of this large developmentally regulated domain of hypomethylation supports a mechanistic role for DNA methylation in developmental regulation of globin genes.
DOI
10.1128/MCB.02234-06
Original Citation
Hsu M, Mabaera R, Lowrey CH, Martin DI, Fiering S. CpG hypomethylation in a large domain encompassing the embryonic beta-like globin genes in primitive erythrocytes. Mol Cell Biol. 2007 Jul;27(13):5047-54. doi: 10.1128/MCB.02234-06. Epub 2007 Apr 23. PMID: 17452448; PMCID: PMC1951500.
Dartmouth Digital Commons Citation
Hsu, Mei; Mabaera, Rodwell R.; Lowrey, Christopher H.; Martin, David I. K.; and Fiering, Steven, "CpG Hypomethylation in a Large Domain Encompassing the Embryonic β-Like Globin Genes in Primitive Erythrocytes" (2007). Dartmouth Scholarship. 1144.
https://digitalcommons.dartmouth.edu/facoa/1144
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