Bigas A, Martin D I, Milner L A
The Fred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024, USA.
Mol Cell Biol. 1998 Apr;18(4):2324-33. doi: 10.1128/MCB.18.4.2324.
We have compared the ability of two mammalian Notch homologs, mouse Notchl and Notch2, to inhibit the granulocytic differentiation of 32D myeloid progenitor cells. 32D cells undergo granulocytic differentiation when stimulated with either granulocyte colony-stimulating factor (G-CSF) or granulocyte-macrophage colony-stimulating factor (GM-CSF). Expression of the activated intracellular domain of Notch1 inhibits the differentiation induced by G-CSF but not by GM-CSF; conversely, the corresponding domain of Notch2 inhibits differentiation in response to GM-CSF but not to G-CSF. The region immediately C-terminal to the cdc10 domain of Notch confers cytokine specificity on the cdc10 domain. The cytokine response patterns of Notch1 and Notch2 are transferred with this region, which we have termed the Notch cytokine response (NCR) region. The NCR region is also associated with differences in posttranslational modification and subcellular localization of the different Notch molecules. These findings suggest that the multiple forms of Notch found in mammals have structural differences that allow their function to be modulated by specific differentiation signals.
我们比较了两种哺乳动物Notch同源物——小鼠Notch1和Notch2抑制32D髓系祖细胞向粒细胞分化的能力。当用粒细胞集落刺激因子(G-CSF)或粒细胞-巨噬细胞集落刺激因子(GM-CSF)刺激时,32D细胞会发生粒细胞分化。Notch1活化的细胞内结构域的表达可抑制G-CSF诱导的分化,但不能抑制GM-CSF诱导的分化;相反,Notch2的相应结构域可抑制对GM-CSF而非G-CSF的分化反应。Notch的cdc10结构域紧邻的C末端区域赋予cdc10结构域细胞因子特异性。Notch1和Notch2的细胞因子反应模式通过这个我们称为Notch细胞因子反应(NCR)区域的区域进行传递。NCR区域还与不同Notch分子的翻译后修饰和亚细胞定位差异有关。这些发现表明,哺乳动物中发现的多种Notch形式具有结构差异,使其功能能够被特定的分化信号调节。