Expression of SCL is normal in transfusion-dependent diamond-blackfan anemia but other bHLH proteins are deficient

被引:17
作者
Zhang, MY
Clawson, GA
Olivieri, NF
Bell, LL
Begley, CG
Miller, BA
机构
[1] PENN STATE UNIV,MILTON S HERSHEY MED CTR,DEPT PEDIAT,COLL MED,HERSHEY,PA 17033
[2] PENN STATE UNIV,MILTON S HERSHEY MED CTR,COLL MED,DEPT PATHOL,HERSHEY,PA 17033
[3] PENN STATE UNIV,MILTON S HERSHEY MED CTR,COLL MED,DEPT BIOCHEM & MOL BIOL,HERSHEY,PA 17033
[4] HOSP SICK CHILDREN,DIV HEMATOL ONCOL,TORONTO,ON M5G 1X8,CANADA
[5] ROYAL MELBOURNE HOSP,WALTER & ELIZA HALL INST MED RES,MELBOURNE,VIC,AUSTRALIA
关键词
D O I
10.1182/blood.V90.5.2068
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:2068 / 2074
页数:7
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