4.5 Article

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

期刊

MOLECULAR AND CELLULAR BIOLOGY
卷 24, 期 17, 页码 7779-7794

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.24.17.7779-7794.2004

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资金

  1. NCI NIH HHS [CA93735, R01 CA093735, CA100057, R01 CA100057, R56 CA100057] Funding Source: Medline
  2. NHLBI NIH HHS [K08 HL04017, K08 HL004017] Funding Source: Medline

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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.

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