| Literature DB >> 21558417 |
Mi-Yeon Kim1, Jung-Soon Mo, Eun-Jung Ann, Ji-Hye Yoon, Jane Jung, Yun-Hee Choi, Su-Man Kim, Hwa-Young Kim, Ji-Seon Ahn, Hangun Kim, Kwonseop Kim, Hyang-Sook Hoe, Hee-Sae Park.
Abstract
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 γ-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.Entities:
Mesh:
Substances:
Year: 2011 PMID: 21558417 DOI: 10.1242/jcs.076117
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285