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

被引:214
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
相关论文
共 32 条
  • [1] Beatus P, 1998, J NEUROSCI RES, V54, P125, DOI 10.1002/(SICI)1097-4547(19981015)54:2<125::AID-JNR1>3.0.CO
  • [2] 2-G
  • [3] A novel proteolytic cleavage involved in Notch signaling:: The role of the disintegrin-metalloprotease TACE
    Brou, C
    Logeat, F
    Gupta, N
    Bessia, C
    LeBail, O
    Doedens, JR
    Cumano, A
    Roux, P
    Black, RA
    Israël, A
    [J]. MOLECULAR CELL, 2000, 5 (02) : 207 - 216
  • [4] split ends, a new component of the Drosophila EGF receptor pathway, regulates development of midline glial cells
    Chen, FL
    Rebay, I
    [J]. CURRENT BIOLOGY, 2000, 10 (15) : 943 - 946
  • [5] PRIMARY NEUROGENESIS IN XENOPUS EMBRYOS REGULATED BY A HOMOLOG OF THE DROSOPHILA NEUROGENIC GENE-DELTA
    CHITNIS, A
    HENRIQUE, D
    LEWIS, J
    ISHHOROWICZ, D
    KINTNER, C
    [J]. NATURE, 1995, 375 (6534) : 761 - 766
  • [6] A presenilin-1-dependent γ-secretase-like protease mediates release of Notch intracellular domain
    De Strooper, B
    Annaert, W
    Cupers, P
    Saftig, P
    Craessaerts, K
    Mumm, JS
    Schroeter, EH
    Schrijvers, V
    Wolfe, MS
    Ray, WJ
    Goate, A
    Kopan, R
    [J]. NATURE, 1999, 398 (6727) : 518 - 522
  • [7] THE RECOMBINATION SIGNAL SEQUENCE-BINDING PROTEIN RBP-2N FUNCTIONS AS A TRANSCRIPTIONAL REPRESSOR
    DOU, SB
    ZENG, XO
    CORTES, P
    ERDJUMENTBROMAGE, H
    TEMPST, P
    HONJO, T
    VALES, LD
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (05) : 3310 - 3319
  • [8] Egan SE, 1998, CURR TOP MICROBIOL, V228, P273
  • [9] Mastermind mediates chromatin-specific transcription and turnover of the Notch enhancer complex
    Fryer, CJ
    Lamar, E
    Turbachova, I
    Kintner, C
    Jones, KA
    [J]. GENES & DEVELOPMENT, 2002, 16 (11) : 1397 - 1411
  • [10] HARLAND RM, 1991, METHOD CELL BIOL, V36, P685