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

Author:

Kim Mi-Yeon1,Mo Jung-Soon1,Ann Eun-Jung1,Yoon Ji-Hye1,Jung Jane1,Choi Yun-Hee1,Kim Su-Man1,Kim Hwa-Young1,Ahn Ji-Seon1,Kim Hangun2,Kim Kwonseop2,Hoe Hyang-Sook3,Park Hee-Sae1

Affiliation:

1. Hormone Research Center, School of Biological Sciences and Technology, Chonnam National University, Gwangju 500-757, Republic of Korea

2. The College of Pharmacy and Research Institute for Drug Development, Chonnam National University, Gwangju 500-757, Republic of Korea

3. Department of Neuroscience and Neurology, Department of Neurology, Georgetown University Medical Center, Washington, DC 20007, USA

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.

Publisher

The Company of Biologists

Subject

Cell Biology

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