NDRG2 and PRA1 interact and synergistically inhibit T-cell factor/beta-catenin signaling

  • Kim, Jong-Tae; 
  • Kim, Jae Wha; 
  • Kang, Yun Hee; 
  • Kim, Kwang Dong; 
  • Lee, Seon-Jin; 
  • 외 6명
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초록

NDRG2 is a member of the N-myc downstream regulated gene (NDRG) family, implicated in cell growth and differentiation. Investigation of NDRG2 molecular interactions by yeast two-hybrid screening identified prenylated Rab acceptor-1 (PRA1), involved in vesicle trafficking and protein transport, as binding partner. Binding of NDRG2 (and NDRG1-4) with PRA1 in vitro was confirmed by GST pull-down assay and immunoprecipitation, and colocalization was verified by confocal microscopy in HCT116 cells. Intracellular coexpression showed that NDRG2 and PRA1 synergistically downregulate T-cell factor (TCF) promoter activity and GSK3 beta phosphorylation. Results suggest that NDRG2 and PRA1 might act synergistically to prevent signaling of TCF/beta-catenin. Structured summary of protein interactions: NDRG2a binds to PRA1 by pull down (View interaction) NDRG2a physically interacts with PRA1 by two hybrid (View Interaction: 1, 2) PRA1 physically interacts with NDRG2a by anti tag coimmunoprecipitation (View interaction) NDRG2a, PRA1 and Catenin beta colocalize by cosedimentation (View interaction) NDRG2a and PRA1 colocalize by fluorescence microscopy (View Interaction: 1, 2, 3) (c) 2012 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

키워드

NDRG; PRA1; Protein-protein interaction; Yeast two-hybrid screen; Promoter inhibition; Cell proliferation; PROSTATE-CANCER CELLS; TUMOR-SUPPRESSOR GENE; BETA-CATENIN; COLORECTAL-CANCER; COLON-CARCINOMA; MYC; EXPRESSION; FAMILY; GROWTH; DIFFERENTIATION
제목
NDRG2 and PRA1 interact and synergistically inhibit T-cell factor/beta-catenin signaling
저자
Kim, Jong-Tae; Kim, Jae Wha; Kang, Yun Hee; Kim, Kwang Dong; Lee, Seon-Jin; Choi, Seung-Chul; Kim, Kwang Soo; Chae, Suhn-Kee; Kim, Jung Woo; Lim, Jong-Seok; Lee, Hee Gu
DOI
10.1016/j.febslet.2012.09.045
발행일
2012-11-16
유형
Article
저널명
FEBS Letters
권
586
호
22
페이지
3962 ~ 3968