首页> 外文期刊>Journal of Cell Science >Regulation of Notch1 signaling by the APP intracellular domain facilitates degradation of the Notch1 intracellular domain and RBP-Jk.
【24h】

Regulation of Notch1 signaling by the APP intracellular domain facilitates degradation of the Notch1 intracellular domain and RBP-Jk.

机译:APP细胞内域对Notch1信号的调节促进了Notch1细胞内域和RBP-Jk的降解。

获取原文
获取原文并翻译 | 示例
           

摘要

The Notch1 receptor is a crucial controller of cell fate decisions, and is also a key regulator of cell growth and differentiation in a variety of contexts. In this study, we have demonstrated that the APP intracellular domain (AICD) attenuates Notch1 signaling by accelerated degradation of the Notch1 intracellular domain (Notch1-IC) and RBP-Jk, through different degradation pathways. AICD suppresses Notch1 transcriptional activity by the dissociation of the Notch1-IC-RBP-Jk complex after processing by gamma-secretase. Notch1-IC is capable of forming a trimeric complex with Fbw7 and AICD, and AICD enhances the protein degradation of Notch1-IC through an Fbw7-dependent proteasomal pathway. AICD downregulates the levels of RBP-Jk protein through the lysosomal pathway. AICD-mediated degradation is involved in the preferential degradation of non-phosphorylated RBP-Jk. Collectively, our results demonstrate that AICD functions as a negative regulator in Notch1 signaling through the promotion of Notch1-IC and RBP-Jk protein degradation.
机译:Notch1受体是决定细胞命运的关键控制器,也是在多种情况下细胞生长和分化的关键调节剂。在这项研究中,我们已经证明,APP细胞内结构域(AICD)通过加速降解Notch1细胞内结构域(Notch1-IC)和RBP-Jk,通过不同的降解途径来减弱Notch1信号传导。 AICD通过由γ-分泌酶处理后,Notch1-IC-RBP-Jk复合体的解离抑制Notch1转录活性。 Notch1-IC能够与Fbw7和AICD形成三聚体复合物,而AICD通过Fbw7依赖性蛋白酶体途径增强Notch1-IC的蛋白质降解。 AICD通过溶酶体途径下调RBP-Jk蛋白的水平。 AICD介导的降解涉及非磷酸化RBP-Jk的优先降解。总的来说,我们的结果表明AICD通过促进Notch1-IC和RBP-Jk蛋白降解,在Notch1信号传导中起负调控作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号