Haltiwanger Robert S, Stanley Pamela
Department of Biochemistry and Cell Biology, Institute for Cell and Developmental Biology, State University of New York-Stony Brook, 11794-5215, USA.
Biochim Biophys Acta. 2002 Dec 19;1573(3):328-35. doi: 10.1016/s0304-4165(02)00400-2.
The Notch family of signaling receptors plays key roles in determining cell fate and growth control. Recently, a number of laboratories have shown that O-fucose glycans on the epidermal growth factor (EGF)-like repeats of the Notch extracellular domain modulate Notch signaling. Fringe, a known modifier of Notch function, is an O-fucose specific beta1,3-N-acetylglucosaminyltransferase. The transfer of GlcNAc to O-fucose on Notch by fringe results in the potentiation of signaling by the Delta class of Notch ligands, but causes inhibition of signaling by the Serrate/Jagged class of Notch ligands. Interestingly, addition of a beta1,4 galactose by beta4GalT-1 to the GlcNAc added by fringe is required for Jagged1-induced Notch signaling to be inhibited in a co-culture assay. Thus, both fringe and beta4GalT-1 are modulators of Notch function. Several models have been proposed to explain how alterations in O-fucose glycans result in changes in Notch signaling, and these models are discussed.
信号受体的Notch家族在决定细胞命运和生长控制方面发挥着关键作用。最近,许多实验室表明,Notch细胞外结构域的表皮生长因子(EGF)样重复序列上的O-岩藻糖聚糖可调节Notch信号传导。Fringe是一种已知的Notch功能调节剂,是一种O-岩藻糖特异性β1,3-N-乙酰葡糖胺基转移酶。Fringe将GlcNAc转移到Notch上的O-岩藻糖上,导致Delta类Notch配体的信号增强,但会抑制Serrate/Jagged类Notch配体的信号传导。有趣的是,在共培养试验中,Jagged1诱导的Notch信号传导被抑制需要β4GalT-1将β1,4半乳糖添加到Fringe添加的GlcNAc上。因此,Fringe和β4GalT-1都是Notch功能的调节剂。已经提出了几种模型来解释O-岩藻糖聚糖的改变如何导致Notch信号传导的变化,并对这些模型进行了讨论。