Fine-tuning of the intracellular canonical Notch signaling pathway

被引:102
作者
Borggrefe, Tilman [1 ]
Liefke, Robert [2 ,3 ]
机构
[1] Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany
[2] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA USA
[3] Childrens Hosp, Div Newborn Med, Boston, MA 02115 USA
关键词
Notch signaling; transcriptional regulation; histone modifications; feedback loops; cell type specificity; ANKYRIN REPEAT DOMAIN; T-CELL DEVELOPMENT; TRANSCRIPTIONAL COACTIVATOR MAML1; MAJOR DOWNSTREAM EFFECTOR; MOLECULAR-WEIGHT NOTCH; DNA-BINDING PROTEIN; RBP-J-KAPPA; HISTONE MODIFICATIONS; COREPRESSOR COMPLEX; FUNCTIONAL INTERACTION;
D O I
10.4161/cc.11.2.18995
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Notch signaling plays a pivotal role in the regulation of many fundamental cellular processes, such as proliferation, stem cell maintenance and differentiation during embryonic and adult development. At the molecular level, ligand binding induces the proteolytic cleavage of the Notch receptor. The intracellular domain of Notch translocates subsequently into the nucleus, associates with the central transcription factor RBP-J and activates transcription. Although, this pathway is remarkably short, with no second messenger involved, it regulates expression of more than hundred target genes in a tissue-specific manner. This review summarizes recent studies on transcriptional and chromatin control mechanisms, which set the stage for specific expression of Notch target genes. Furthermore, we review how the canonical (RBP-J dependent) Notch pathway is fine-tuned by downstream effectors and feedback loops in mammals.
引用
收藏
页码:264 / 276
页数:13
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