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   <subfield code="a">Epigenetic Modifications and Chromosome Conformations of the Beta Globin Locus throughout Development</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Kai-Hsin Chang, Xiangdong Fang, Hao Wang, Andy Huang, Hua Cao, Yadong Yang, Halvard Bonig, John Stamatoyannopoulos, Thalia Papayannopoulou]</subfield>
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   <subfield code="a">Human embryonic stem cells provide an alternative to using human embryos for studying developmentally regulated gene expression. The co-expression of high levels of embryonic ε and fetal γ globin by the hESC-derived erythroblasts allows the interrogation of ε globin regulation at the transcriptional and epigenetic level which could only be attained previously by studying cell lines or transgenic mice. In this study, we compared the histone modifications across the β globin locus of the undifferentiated hESCs and hESC-, FL-, and mobilized PB CD34+ cells-derived erythroblasts, which have distinct globin expression patterns corresponding to their developmental stages. We demonstrated that the histone codes employed by the β globin locus are conserved throughout development. Furthermore, in spite of the close proximity of the ε globin promoter, as compared to the β or γ globin promoter, with the LCR, a chromatin loop was also formed between the LCR and the active ε globin promoter, similar to the loop that forms between the β or γ globin promoters and the LCR, in contrary to the previously proposed tracking mechanism.</subfield>
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   <subfield code="a">Human embryonic stem cells</subfield>
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   <subfield code="a">Erythroid cells</subfield>
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   <subfield code="a">Fetal liver</subfield>
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   <subfield code="a">Peripheral blood</subfield>
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   <subfield code="a">Erythroblasts</subfield>
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   <subfield code="u">Department of Medicine, Division of Hematology, University of Washington, NE Pacific St, Box 357710, 98195, Seattle, WA, USA</subfield>
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   <subfield code="t">Stem Cell Reviews and Reports</subfield>
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