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

被引:17
|
作者
Kim, Mi-Yeon [1 ]
Mo, Jung-Soon [1 ]
Ann, Eun-Jung [1 ]
Yoon, Ji-Hye [1 ]
Jung, Jane [1 ]
Choi, Yun-Hee [1 ]
Kim, Su-Man [1 ]
Kim, Hwa-Young [1 ]
Ahn, Ji-Seon [1 ]
Kim, Hangun [2 ]
Kim, Kwonseop [2 ]
Hoe, Hyang-Sook [3 ]
Park, Hee-Sae [1 ]
机构
[1] Chonnam Natl Univ, Sch Biol Sci & Technol, Hormone Res Ctr, Kwangju 500757, South Korea
[2] Chonnam Natl Univ, Coll Pharm & Res, Inst Drug Dev, Kwangju 500757, South Korea
[3] Georgetown Univ, Dept Neurosci & Neurol, Dept Neurol, Med Ctr, Washington, DC 20007 USA
关键词
APP; Notch1; Protein degradation; AMYLOID PRECURSOR PROTEIN; MUSCLE-CELL DIFFERENTIATION; GAMMA-SECRETASE CLEAVAGE; C-TERMINAL FRAGMENT; ALZHEIMERS-DISEASE; ACTIVATE TRANSCRIPTION; PHYSICAL INTERACTION; PRESOMITIC MESODERM; COREPRESSOR COMPLEX; MAMMALIAN-CELLS;
D O I
10.1242/jcs.076117
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
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.
引用
收藏
页码:1831 / 1843
页数:13
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