Department of Molecular Biochemistry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Dev Growth Differ. 2020 Jan;62(1):35-48. doi: 10.1111/dgd.12643. Epub 2019 Dec 30.
Notch signaling is an evolutionarily conserved signaling pathway and is essential for cell-fate specification in metazoans. Dysregulation of Notch signaling results in various human diseases, including cardiovascular defects and cancer. In 2000, Fringe, a known regulator of Notch signaling, was discovered as a Notch-modifying glycosyltransferase. Since then, glycosylation-a post-translational modification involving literal sugars-on the Notch extracellular domain has been noted as a critical mechanism for the regulation of Notch signaling. Additionally, the presence of diverse O-glycans decorating Notch receptors has been revealed in the extracellular domain epidermal growth factor-like (EGF) repeats. Here, we concisely summarize the recent studies in the human diseases associated with aberrant Notch glycosylation.
Notch 信号通路是一条进化上保守的信号通路,对于后生动物的细胞命运特化至关重要。 Notch 信号通路的失调会导致各种人类疾病,包括心血管缺陷和癌症。2000 年,Fr i nge 作为 Notch 信号的已知调节剂,被发现是一种 Notch 修饰糖基转移酶。从那时起,Notch 细胞外结构域上的糖基化——一种涉及糖的翻译后修饰——已被认为是 Notch 信号调控的关键机制。此外,在 Notch 受体的细胞外结构域表皮生长因子样(EGF)重复序列中,存在多种 O-聚糖的装饰已被揭示。在这里,我们简要总结了与异常 Notch 糖基化相关的人类疾病的最新研究。