Experimental Hematology
Volume 35, Issue 3 , Pages 358-367, March 2007

Stem cell transplantation demonstrates that Sox6 represses εy globin expression in definitive erythropoiesis of adult mice

  • Orit Cohen-Barak

      Affiliations

    • Department of Pediatrics, University of Arizona, College of Medicine, Tucson, Ariz., USA
    • These authors contributed equally to this work.
  • ,
  • Drew T. Erickson

      Affiliations

    • Department of Pediatrics, University of Arizona, College of Medicine, Tucson, Ariz., USA
    • These authors contributed equally to this work.
  • ,
  • Michael S. Badowski

      Affiliations

    • Department of Immunology, University of Arizona, College of Medicine, Tucson, Ariz., USA
  • ,
  • Deborah A. Fuchs

      Affiliations

    • Department of Pathology, University of Arizona, College of Medicine, Tucson, Ariz., USA
  • ,
  • Christine L. Klassen

      Affiliations

    • Department of Pediatrics, University of Arizona, College of Medicine, Tucson, Ariz., USA
  • ,
  • David T. Harris

      Affiliations

    • Department of Immunology, University of Arizona, College of Medicine, Tucson, Ariz., USA
  • ,
  • Murray H. Brilliant

      Affiliations

    • Department of Pediatrics, University of Arizona, College of Medicine, Tucson, Ariz., USA
    • Corresponding Author InformationOffprint requests to: Murray H. Brilliant, Ph.D., University of Arizona College of Medicine Department of Pediatrics, Steele Children's Research Center 1501 N. Campbell Ave. Tucson, AZ 85724

Sox6, a member of the Sox transcription factor family, is essential for the silencing of εy globin gene expression in definitive erythropoiesis of mice. Homozygous Sox6-null mice are neonatally lethal, precluding analysis at later stages. We created adult mice that are deficient in Sox6 specifically in hematopoietic tissues by transplanting embryonic liver stem cells from Sox6-deficient mice into lethally irradiated congenic wild-type adult mice. The mice receiving mutant stem cells (mutant engrafted) showed high expression levels of εy in bone marrow, spleen, and circulating blood compared with mice receiving wild-type and heterozygous stem cells (control engrafted). The level of expression of εy in circulating blood was directly correlated with the percentage of successful mutant donor cell engraftment. Additionally, the mutant engrafted adult mice showed an increase in erythroid precursor cells in bone marrow, spleen, and blood. Thus, Sox6 continues to function as a major regulator of εy in adult definitive erythropoiesis and is required for normal erythrocyte maturation. Therefore, Sox6 may provide a novel therapeutic target by reactivating εy in patients with hemoglobinopathies such as sickle cell anemia and beta-thalassemia.

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PII: S0301-472X(06)00703-X

doi:10.1016/j.exphem.2006.11.009

Experimental Hematology
Volume 35, Issue 3 , Pages 358-367, March 2007