SHARP is a novel component of the Notch/RBP-Jκ signalling pathway

被引:215
作者
Oswald, F
Kostezka, U
Astrahantseff, K
Bourteele, S
Dillinger, K
Zechner, U
Ludwig, L
Wilda, M
Hameister, H
Knöchel, W
Liptay, S
Schmid, RM
机构
[1] Univ Ulm, Dept Internal Med, D-89081 Ulm, Germany
[2] Univ Ulm, Dept Human Genet, D-89081 Ulm, Germany
[3] Univ Ulm, Dept Biochem, D-89081 Ulm, Germany
关键词
corepressor; gene expression; Notch; RBP-J kappa; SHARP;
D O I
10.1093/emboj/cdf549
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
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.
引用
收藏
页码:5417 / 5426
页数:10
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