The first deltex null mutant indicates tissue-specific deltex-dependent Notch signaling in Drosophila

被引:49
作者
Fuwa, TJ
Hori, K
Sasamura, T
Higgs, J
Baron, M
Matsuno, K
机构
[1] Tokyo Univ Sci, Dept Biol Sci & Technol, Noda, Chiba 2788510, Japan
[2] PRESTO, Japan Sci & Technol Agcy, Kawaguchi, Saitama, Japan
[3] Univ Manchester, Fac Life Sci, Manchester M13 9PT, Lancs, England
基金
英国生物技术与生命科学研究理事会;
关键词
Deltex; Notch; Notch signaling; Suppressor of Hairless; Drosophila;
D O I
10.1007/s00438-005-0087-3
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 (N) is a single-pass transmembrane receptor. The N signaling pathway is an evolutionarily conserved mechanism that controls various cell-specification processes. Drosophila Deltex (Dx), a RING-domain E3 ubiquitin ligase, binds to the N intracellular domain, promotes N's endocytic trafficking to late endosomes, and was proposed to activate Suppressor of Hairless [Su(H)]-independent N signaling. However, it has been difficult to evaluate the importance of dx, because no null mutant of a dx family gene has been available in any organism. Here, we report the first null mutant allele of Drosophila dx. We found that dx was involved only in the subsets of N signaling, but was not essential for it in any developmental context. A strong genetic interaction between dx and Su(H) suggested that dx might function in Su(H)-dependent N signaling. Our epistatic analyses suggested that dx functions downstream of the ligands and upstream of activated Su(H). We also uncovered a novel dx activity that suppressed N signaling downstream of N.
引用
收藏
页码:251 / 263
页数:13
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