Down syndrome critical region 1 (DSCR1) is recognized as an endogenous calcineurin inhibitor. DSCR1 is induced in endothelial cells and may play an important role in inflammation and angiogenesis. To address a novel function of DSCR1, we searched interacting partners of DSCR1. We performed pull-down analysis using DSCR1 as a bait and identified Raf-1 as a binding partner. The association of Raf-1 was confirmed by co-immunoprecipitation in GM7373 cells expressing green fluorescence protein tagged DSCR1. We determined two Raf-1 binding regions in DSCR1; one in the N-terminus and the other in the C-terminus regions. We further demonstrated that calpain cleaved DSCR1 and generated fragments with different binding affinity to Raf-1 or calcineurin. These results constitute the first demonstration of Raf-1 as a binding partner of DSCR1, and suggest a novel role of DSCR1. (C) 2005 Elsevier Inc. All rights reserved.
机构:
Inst Canc Res, Signal Transduct Team, Canc Res UK Ctr Cell & Mol Biol, London SW3 6JB, EnglandInst Canc Res, Signal Transduct Team, Canc Res UK Ctr Cell & Mol Biol, London SW3 6JB, England
Dumaz, N
Marais, R
论文数: 0引用数: 0
h-index: 0
机构:
Inst Canc Res, Signal Transduct Team, Canc Res UK Ctr Cell & Mol Biol, London SW3 6JB, EnglandInst Canc Res, Signal Transduct Team, Canc Res UK Ctr Cell & Mol Biol, London SW3 6JB, England
机构:
NCI, Regulat Cell Growth Lab, Frederick Canc Res & Dev Ctr, Frederick, MD 21702 USANCI, Regulat Cell Growth Lab, Frederick Canc Res & Dev Ctr, Frederick, MD 21702 USA
Müller, J
Morrison, DK
论文数: 0引用数: 0
h-index: 0
机构:NCI, Regulat Cell Growth Lab, Frederick Canc Res & Dev Ctr, Frederick, MD 21702 USA
Morrison, DK
G PROTEIN PATHWAYS: PT C, EFFECTOR MECHANISMS,
2002,
345
: 490
-
498