Expression of SCL is normal in transfusion-dependent diamond-blackfan anemia but other bHLH proteins are deficient
Details
Publication Year 1997-09-01,Volume 90,Issue #5,Page 2068-2074
Journal Title
BLOOD
Publication Type
Journal Article
Abstract
Basic helix-loop-helix proteins, which are tissue specific (SCL) or broadly expressed (E proteins), interact positively to regulate erythroid specific genes. Here, expression of SCL and two broadly expressed E proteins, E47 and HEB, was high early in erythroid differentiation and declined during maturation. Stimulation of erythroid progenitors/precursors with stem cell factor (SCF) enhanced SCL acid E protein levels, one mechanism by which SCF may increase erythroid proliferation. Interactions between SCL and E proteins are competed by Id2, which binds and sequesters E proteins, Upregulation of Id2, demonstrated here late in erythroid differentiation, may downregulate genes involved in erythroid proliferation/differentiation. We examined expression of bHLH proteins in transfusion-dependent patients with Diamond-Blackfan anemia (DBA) to determine if these interactions are disrupted. In erythroblasts from patients, expression of SCL protein and mRNA was normal and SCL increased in response to SCF. However, E47 and HEB protein levels were significantly decreased. Id2 was strongly expressed in patients, Through reduction of SCL/E protein heterodimer formation, abnormal levels of bHLH transcription factors may affect expression of erythroid specific genes, such as beta globin. Stimulation of Diamond-Blackfan cells with SCF partially compensated for this defect, enhancing expression of E47, HEB, and SCL. SCF may function to increase SCL/E protein heterodimer formation, which may be one of the mechanisms through which SCF stimulates erythroid proliferation/differentiation in DBA. (C) 1997 by The American Society of Hematology.
Publisher
W B SAUNDERS CO
Keywords
STEM-CELL FACTOR; LOOP-HELIX PROTEINS; DNA-BINDING; TRANSCRIPTION FACTOR; ERYTHROID-DIFFERENTIATION; C-KIT; PROGENITOR CELLS; GENE-PRODUCT; RECEPTOR; INVITRO
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Creation Date: 1997-09-01 12:00:00
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