Notch signaling: simplicity in design, versatility in function

被引:728
作者
Andersson, Emma R. [1 ]
Sandberg, Rickard [2 ]
Lendahl, Urban [1 ]
机构
[1] Karolinska Inst, Dept Cell & Mol Biol, SE-17177 Stockholm, Sweden
[2] Karolinska Inst, Ludwig Inst Canc Res, SE-17177 Stockholm, Sweden
来源
DEVELOPMENT | 2011年 / 138卷 / 17期
基金
欧洲研究理事会; 瑞典研究理事会;
关键词
Cis-inhibition; Delta-like; Signaling diversity; Jagged; Notch; Notch intracellular domain; ACUTE LYMPHOBLASTIC-LEUKEMIA; AMYLOID PRECURSOR PROTEIN; JAGGED1; JAG1; MUTATIONS; ABNORMAL VERTEBRAL SEGMENTATION; AUTOSOMAL-DOMINANT ARTERIOPATHY; ANKYRIN REPEAT DOMAIN; SMOOTH-MUSCLE-CELLS; LUNATIC-FRINGE GENE; KAPPA-B ACTIVITY; GAMMA-SECRETASE;
D O I
10.1242/dev.063610
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Notch signaling is evolutionarily conserved and operates in many cell types and at various stages during development. Notch signaling must therefore be able to generate appropriate signaling outputs in a variety of cellular contexts. This need for versatility in Notch signaling is in apparent contrast to the simple molecular design of the core pathway. Here, we review recent studies in nematodes, Drosophila and vertebrate systems that begin to shed light on how versatility in Notch signaling output is generated, how signal strength is modulated, and how cross-talk between the Notch pathway and other intracellular signaling systems, such as the Wnt, hypoxia and BMP pathways, contributes to signaling diversity.
引用
收藏
页码:3593 / 3612
页数:20
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