Role of conserved intracellular motifs in Serrate signalling, cis-inhibition and endocytosis

被引:99
作者
Glittenberg, Marcus
Pitsouli, Chrysoula
Garvey, Clare
Delidakis, Christos
Bray, Sarah
机构
[1] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 3DY, England
[2] FORTH, Inst Mol Biol & Biotechnol, Iraklion, Greece
[3] Univ Crete, Dept Biol, Iraklion, Greece
基金
英国医学研究理事会;
关键词
Drosophila; endocytosis; notch; Serrate; ubiquitination;
D O I
10.1038/sj.emboj.7601337
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 is the receptor in a signalling pathway that operates in a diverse spectrum of developmental processes. Its ligands (e.g. Serrate) are transmembrane proteins whose signalling competence is regulated by the endocytosis-promoting E3 ubiquitin ligases, Mindbomb1 and Neuralized. The ligands also inhibit Notch present in the same cell (cis-inhibition). Here, we identify two conserved motifs in the intracellular domain of Serrate that are required for efficient endocytosis. The first, a dileucine motif, is dispensable for trans-activation and cis-inhibition despite the endocytic defect, demonstrating that signalling can be separated from bulk endocytosis. The second, a novel motif, is necessary for interactions with Mindbomb1/Neuralized and is strictly required for Serrate to trans-activate and internalise efficiently but not for it to inhibit Notch signalling. Cis-inhibition is compromised when an ER retention signal is added to Serrate, or when the levels of Neuralized are increased, and together these data indicate that cis-inhibitory interactions occur at the cell surface. The balance of ubiquitinated/ unubiquitinated ligand will thus affect the signalling capacity of the cell at several levels.
引用
收藏
页码:4697 / 4706
页数:10
相关论文
共 47 条
[1]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[2]   Signals for sorting of transmembrane proteins to endosomes and lysosomes [J].
Bonifacino, JS ;
Traub, LM .
ANNUAL REVIEW OF BIOCHEMISTRY, 2003, 72 :395-447
[3]   The carboxyl-terminal valine residues of ProTGF alpha are required for its efficient maturation and intracellular routing [J].
Briley, GP ;
Hissong, MA ;
Chiu, ML ;
Lee, DC .
MOLECULAR BIOLOGY OF THE CELL, 1997, 8 (08) :1619-1631
[4]   Glycosyltransferase activity of fringe modulates notch-delta interactions [J].
Brückner, K ;
Perez, L ;
Clausen, H ;
Cohen, S .
NATURE, 2000, 406 (6794) :411-415
[5]   Spatially restricted factors cooperate with Notch in the regulation of Enhancer of split genes [J].
Cooper, MTD ;
Tyler, DM ;
Furriols, M ;
Chalkiadaki, A ;
Delidakis, C ;
Bray, S .
DEVELOPMENTAL BIOLOGY, 2000, 221 (02) :390-403
[6]  
de Celis JF, 1998, DEVELOPMENT, V125, P4617
[7]  
deCelis JF, 1996, DEVELOPMENT, V122, P359
[8]  
deCelis JF, 1997, DEVELOPMENT, V124, P3241
[9]   Gradient formation of the TGF-β homolog Dpp [J].
Entchev, EV ;
Schwabedissen, A ;
González-Gaitán, M .
CELL, 2000, 103 (06) :981-991
[10]   Structural conservation of Notch receptors and ligands [J].
Fleming, RJ .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 1998, 9 (06) :599-607