Jun blockade of erythropoiesis: Role for repression of GATA-1 by HERP2

被引:57
作者
Elagib, KE
Xiao, M
Hussaini, IM
Delehanty, LL
Palmer, LA
Racke, FK
Birrer, MJ
Shanmugasundaram, G
McDevitt, MA
Goldfarb, AN
机构
[1] Univ Virginia, Sch Med, Dept Pathol, Charlottesville, VA 22908 USA
[2] Univ Virginia, Sch Med, Dept Pediat, Charlottesville, VA 22908 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[5] NCI, Mol Mechanism Sect, Rockville, MD USA
关键词
D O I
10.1128/MCB.24.17.7779-7794.2004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although Jun upregulation and activation have been established as critical to oncogenesis, the relevant downstream pathways remain incompletely characterized. In this study, we found that c-Jun blocks erythroid differentiation in primary human hematopoietic progenitors and, correspondingly, that Jun factors block transcriptional activation by GATA-1, the central regulator of erythroid differentiation. Mutagenesis of c-Jun suggested that its repression of GATA-1 occurs through a transcriptional mechanism involving activation of downstream genes. We identified the hairy-enhancer-of-split-related factor HERP2 as a novel gene upregulated by c-Jun. HERP2 showed physical interaction with GATA-1 and repressed GATA-1 transcriptional activation. Furthermore, transduction of HERP2 into primary human hematopoietic progenitors inhibited erythroid differentiation. These results thus define a novel regulatory pathway linking the transcription factors c-Jun, HERP2, and GATA-1. Furthermore, these results establish a connection between the Notch signaling pathway, of which the HERP factors are a critical component, and the GATA family, which participates in programming of cellular differentiation.
引用
收藏
页码:7779 / 7794
页数:16
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