Oswald Franz, Kostezka Ulrike, Astrahantseff Kathy, Bourteele Soizic, Dillinger Karin, Zechner Ulrich, Ludwig Leopold, Wilda Monika, Hameister Horst, Knöchel Walter, Liptay Susanne, Schmid Roland M
Department of Internal Medicine and Pediatrics, University of Ulm, Robert-Koch-Strasse 8, D-89081 Ulm, Germany.
EMBO J. 2002 Oct 15;21(20):5417-26. doi: 10.1093/emboj/cdf549.
Notch proteins are the receptors for an evolutionarily highly conserved signalling pathway that regulates numerous cell fate decisions during development. Signal transduction involves the presenilin-dependent intracellular processing of Notch and nuclear translocation of the intracellular domain of Notch, Notch-IC. Notch-IC associates with the DNA-binding protein RBP-Jkappa/CBF-1 to activate transcription of Notch target genes. In the absence of Notch signalling, RBP-Jkappa/CBF-1 acts as a transcriptional repressor through the recruitment of histone deacetylase (HDAC) corepressor complexes. We identified SHARP as an RBP-Jkappa/CBF-1-interacting corepressor in a yeast two-hybrid screen. In cotransfection experiments, SHARP-mediated repression was sensitive to the HDAC inhibitor TSA and facilitated by SKIP, a highly conserved SMRT and RBP-Jkappa-interacting protein. SHARP repressed Hairy/Enhancer of split (HES)-1 promoter activity, inhibited Notch-1-mediated transactivation and rescued Notch-1-induced inhibition of primary neurogenesis in Xenopus laevis embryos. Based on our data, we propose a model in which SHARP is a novel component of the HDAC corepressor complex, recruited by RBP-Jkappa to repress transcription of target genes in the absence of activated Notch.
Notch蛋白是一种进化上高度保守的信号通路的受体,该信号通路在发育过程中调节众多细胞命运决定。信号转导涉及Notch的早老素依赖性细胞内加工以及Notch细胞内结构域Notch-IC的核转位。Notch-IC与DNA结合蛋白RBP-Jκ/CBF-1结合以激活Notch靶基因的转录。在没有Notch信号的情况下,RBP-Jκ/CBF-1通过募集组蛋白脱乙酰酶(HDAC)共抑制复合物作为转录抑制因子。我们在酵母双杂交筛选中鉴定出SHARP是一种与RBP-Jκ/CBF-1相互作用的共抑制因子。在共转染实验中,SHARP介导的抑制对HDAC抑制剂TSA敏感,并由SKIP促进,SKIP是一种高度保守的与SMRT和RBP-Jκ相互作用的蛋白。SHARP抑制Hairy/Enhancer of split(HES)-1启动子活性,抑制Notch-1介导的反式激活,并挽救Notch-1诱导的非洲爪蟾胚胎初级神经发生的抑制。基于我们的数据,我们提出了一个模型,其中SHARP是HDAC共抑制复合物的一个新组分,在没有激活的Notch时由RBP-Jκ募集以抑制靶基因的转录。