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细胞内经典 Notch 信号通路的微调。

Fine-tuning of the intracellular canonical Notch signaling pathway.

机构信息

Max-Planck-Institute of Immunobiology and Epigenetics, Freiburg, Germany.

出版信息

Cell Cycle. 2012 Jan 15;11(2):264-76. doi: 10.4161/cc.11.2.18995.

Abstract

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.

摘要

Notch 信号通路在许多基本的细胞过程的调控中起着关键作用,如胚胎和成年发育过程中的增殖、干细胞维持和分化。在分子水平上,配体结合诱导 Notch 受体的蛋白水解切割。随后 Notch 的细胞内结构域转位到细胞核内,与中央转录因子 RBP-J 结合并激活转录。尽管该途径非常简单,不涉及第二信使,但它以组织特异性的方式调节超过一百个靶基因的表达。本综述总结了关于转录和染色质控制机制的最新研究,这些研究为 Notch 靶基因的特异性表达奠定了基础。此外,我们还综述了在哺乳动物中,经典(依赖于 RBP-J 的)Notch 途径如何通过下游效应物和反馈环进行精细调节。

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