<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Getman M</submitter><funding>NIDDK NIH HHS</funding><funding>NHLBI NIH HHS</funding><pagination>536-46.e8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6176860</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>42(7)</volume><pubmed_abstract>Globin gene regulation occurs in the context of a maturing erythroid cell, which is undergoing significant changes in chromatin structure and gene expression. There are few model systems available that facilitate studies of globin gene regulation in the context of erythroid maturation. Extensively self-renewing erythroblasts (ESREs) are a nontransformed model of erythroid maturation derived from murine fetal liver or yolk sac. Imaging flow cytometry and RNA-seq studies demonstrate that ESREs functionally and molecularly model erythroid maturation. To address the need for a model system that also recapitulates human globin switching, ESREs were derived from mice transgenic for the complete human β-globin locus (β-yac ESREs). β-yac ESREs express β-globin from the transgenic human locus, with</pubmed_abstract><journal>Experimental hematology</journal><pubmed_title>Extensively self-renewing erythroblasts derived from transgenic β-yac mice is a novel model system for studying globin switching and erythroid maturation.</pubmed_title><pmcid>PMC6176860</pmcid><funding_grant_id>R01 HL116364</funding_grant_id><funding_grant_id>R01 HL111264</funding_grant_id><funding_grant_id>K08 DK090153</funding_grant_id><pubmed_authors>Peterson K</pubmed_authors><pubmed_authors>Steiner LA</pubmed_authors><pubmed_authors>England SJ</pubmed_authors><pubmed_authors>Palis J</pubmed_authors><pubmed_authors>Getman M</pubmed_authors><pubmed_authors>Malik J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Extensively self-renewing erythroblasts derived from transgenic β-yac mice is a novel model system for studying globin switching and erythroid maturation.</name><description>Globin gene regulation occurs in the context of a maturing erythroid cell, which is undergoing significant changes in chromatin structure and gene expression. There are few model systems available that facilitate studies of globin gene regulation in the context of erythroid maturation. Extensively self-renewing erythroblasts (ESREs) are a nontransformed model of erythroid maturation derived from murine fetal liver or yolk sac. Imaging flow cytometry and RNA-seq studies demonstrate that ESREs functionally and molecularly model erythroid maturation. To address the need for a model system that also recapitulates human globin switching, ESREs were derived from mice transgenic for the complete human β-globin locus (β-yac ESREs). β-yac ESREs express β-globin from the transgenic human locus, with</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jul</publication><modification>2026-05-01T14:19:27.339Z</modification><creation>2019-03-26T23:59:45Z</creation></dates><accession>S-EPMC6176860</accession><cross_references><pubmed>24704162</pubmed><doi>10.1016/j.exphem.2014.03.006</doi></cross_references></HashMap>