JIP1 binding to RBP-Jk mediates cross-talk between the Notch1 and JIP1-JNK signaling pathway
- Authors
- Kim, M-Y; Ann, E-J; Mo, J-S; Dajas-Bailador, F.; Seo, M-S; Hong, J-A; Jung, J.; Choi, Y-H; Yoon, J-H; Kim, S-M; Choi, E-J; Hoe, H-S; Whitmarsh, A. J.; Park, H-S
- Issue Date
- 11월-2010
- Publisher
- NATURE PUBLISHING GROUP
- Keywords
- RBP-Jk; Notch1; JIP1; SH3 domain; cytoplasmic retention
- Citation
- CELL DEATH AND DIFFERENTIATION, v.17, no.11, pp.1728 - 1738
- Indexed
- SCIE
SCOPUS
- Journal Title
- CELL DEATH AND DIFFERENTIATION
- Volume
- 17
- Number
- 11
- Start Page
- 1728
- End Page
- 1738
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/115411
- DOI
- 10.1038/cdd.2010.50
- ISSN
- 1350-9047
- Abstract
- Notch1 signaling has a critical function in maintaining a balance among cell proliferation, differentiation, and apoptosis. Our earlier work showed that the Notch1 intracellular domain interferes with the scaffolding function of c-Jun N-terminal kinase (JNK)-interacting protein-1 (JIP1), yet the effect of JIP1 for Notch1-recombining binding protein suppressor of hairless (RBP-Jk) signaling remains unknown. Here, we show that JIP1 suppresses Notch1 activity. JIP1 was found to physically associate with either intracellular domain of Notch1 or RBP-Jk and interfere with the interaction between them. Furthermore, we ascertained that JIP1 caused the cytoplasmic retention of RBP-Jk through an interaction between the C-terminal region of JIP1 including Src homology 3 domain and the proline-rich domain of RBP-Jk. We also found that RBP-Jk inhibits JIP1-mediated activation of the JNK1 signaling cascade and cell death. Our results suggest that direct protein-protein interactions coordinate cross-talk between the Notch1-RBP-Jk and JIP1-JNK pathways. Cell Death and Differentiation (2010) 17, 1728-1738; doi:10.1038/cdd.2010.50; published online 28 May 2010
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - Graduate School > Department of Life Sciences > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.