Redox regulation of Wnt signalling via nucleoredoxin

被引:72
作者
Funato, Yosuke [1 ]
Miki, Hiroaki [1 ]
机构
[1] Osaka Univ, Inst Prot Res, Lab Intracellular Signaling, Suita, Osaka 5650871, Japan
关键词
PROTEIN PHOSPHATASE 2A; THIOREDOXIN-LIKE PROTEIN; MAMMARY ONCOGENE INT-1; CONE VIABILITY FACTOR; NF-KAPPA-B; BETA-CATENIN; OXIDATIVE STRESS; POLARITY GENE; CAENORHABDITIS-ELEGANS; TISSUE POLARITY;
D O I
10.3109/10715761003610745
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Numerous studies indicate that reactive oxygen species (ROS) are not merely cellular by-products of respiration, but are able to modulate various signalling pathways and play certain physiological roles. Recent studies have revealed the importance of translating ROS-generation to activation/suppression of specific signalling pathways. The Wnt signalling pathway, which is essential for early development and stem cell maintenance, is also regulated by ROS. A thioredoxin-related protein, nucleoredoxin (NRX), governs ROS-stimulated Wnt signalling in a temporal manner. NRX usually interacts with Dishevelled (Dvl), an essential adaptor protein for Wnt signalling, and blocks the activation of the Wnt pathway. Oxidative stress causes dissociation of NRX from Dvl, which enables Dvl to activate the downstream Wnt signalling pathway. This study also presents the latest research findings on NRX and its related molecules.
引用
收藏
页码:379 / 388
页数:10
相关论文
共 90 条
[1]   Oxidative stress antagonizes Wnt signaling in osteoblast precursors by diverting β-catenin from T cell factor- to Forkhead box O-mediated transcription [J].
Almeida, Maria ;
Han, Li ;
Martin-Millan, Marta ;
O'Brien, Charles A. ;
Manolagas, Stavros C. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (37) :27298-27305
[2]   DNA damage responses to oxidative stress [J].
Barzilai, A ;
Yamamoto, KI .
DNA REPAIR, 2004, 3 (8-9) :1109-1115
[3]   A new member of the frizzled family from Drosophila functions as a Wingless receptor [J].
Bhanot, P ;
Brink, M ;
Samos, CH ;
Hsieh, JC ;
Wang, YS ;
Macke, JP ;
Andrew, D ;
Nathans, J ;
Nusse, R .
NATURE, 1996, 382 (6588) :225-230
[4]   Wnt induces LRP6 signalosomes and promotes dishevelled-dependent LRP6 phosphorylation [J].
Bilic, Josipa ;
Huang, Ya-Lin ;
Davidson, Gary ;
Zimmermann, Timo ;
Cruciat, Cristina-Maria ;
Bienz, Mariann ;
Niehrs, Christof .
SCIENCE, 2007, 316 (5831) :1619-1622
[5]   Discovery of Candidate Disease Genes in ENU-Induced Mouse Mutants by Large-Scale Sequencing, Including a Splice-Site Mutation in Nucleoredoxin [J].
Boles, Melissa K. ;
Wilkinson, Bonney M. ;
Wilming, Laurens G. ;
Liu, Bin ;
Probst, Frank J. ;
Harrow, Jennifer ;
Grafham, Darren ;
Hentges, Kathryn E. ;
Woodward, Lanette P. ;
Maxwell, Andrea ;
Mitchell, Karen ;
Risley, Michael D. ;
Johnson, Randy ;
Hirschi, Karen ;
Lupski, James R. ;
Funato, Yosuke ;
Miki, Hiroaki ;
Marin-Garcia, Pablo ;
Matthews, Lucy ;
Coffey, Alison J. ;
Parker, Anne ;
Hubbard, Tim J. ;
Rogers, Jane ;
Bradley, Allan ;
Adams, David J. ;
Justice, Monica J. .
PLOS GENETICS, 2009, 5 (12)
[6]   Dishevelled activates JNK and discriminates between JNK pathways in planar polarity and wingless signaling [J].
Boutros, M ;
Paricio, N ;
Strutt, DI ;
Mlodzik, M .
CELL, 1998, 94 (01) :109-118
[7]  
Brault V, 2001, DEVELOPMENT, V128, P1253
[8]   Wnt signaling: a common theme in animal development [J].
Cadigan, KM ;
Nusse, R .
GENES & DEVELOPMENT, 1997, 11 (24) :3286-3305
[9]   Rod-derived Cone Viability Factor-2 is a novel bifunctional-thioredoxin-like protein with therapeutic potential [J].
Chalmel, Frederic ;
Leveillard, Thierry ;
Jaillard, Celine ;
Lardenois, Aurelie ;
Berdugo, Naomi ;
Morel, Emmanuelle ;
Koehl, Patrice ;
Lambrou, George ;
Holmgren, Arne ;
Sahel, Jose A. ;
Poch, Olivier .
BMC MOLECULAR BIOLOGY, 2007, 8
[10]   Wnt-1 signaling inhibits apoptosis by activating β-catenin/T cell factor-mediated transcription [J].
Chen, SQ ;
Guttridge, DC ;
You, ZB ;
Zhang, ZC ;
Fribley, A ;
Mayo, MW ;
Kitajewski, J ;
Wang, CY .
JOURNAL OF CELL BIOLOGY, 2001, 152 (01) :87-96