Down-regulation of Notch target gene expression by Suppressor of deltex

被引:39
作者
Mazaleyrat, SL [1 ]
Fostier, M [1 ]
Wilkin, MB [1 ]
Aslam, H [1 ]
Evans, DAP [1 ]
Cornell, M [1 ]
Baron, M [1 ]
机构
[1] Univ Manchester, Sch Biol Sci, Manchester M13 9PT, Lancs, England
基金
英国惠康基金; 英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
Notch; Suppressor of deltex; Drosophila; ubiquitin ligase;
D O I
10.1016/S0012-1606(02)00086-6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In Drosophila, Suppressor of deltex (Su(dx)) mutations display a wing vein gap phenotype resembling that of Notch gain of function alleles. The Su(dx) protein may therefore act as a negative regulator of Notch but its activity on actual Notch signalling levels has not been demonstrated. Here we show that Su(dx) does regulate the level of Notch signalling in vivo, upstream of Notch target genes and in different developmental contexts, including a previously unknown role in leg joint formation. Overexpression of Su(dx) was capable of blocking both the endogenous activity of Notch and the ectopic Notch signalling induced by the overexpression of Deltex, an intracellular Notch binding protein. In addition, using the conditional phenotype of the Su(dx)(sp) allele, we show that loss of Su(dx) activity is rapidly followed by an up-regulation of E(spl)mbeta expression, the immediate target of Notch signal activation during wing vein development. While Su(dx) adult wing vein phenotypes are quite mild, only affecting the distal tips of the veins, we show that the initial consequence of loss of Su(dx) activity is more severe than previously thought. Using a time-course experiment we show that the phenotype is buffered by feedback regulation illustrating how signalling networks can make development robust to perturbation. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:363 / 372
页数:10
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