Tankyrase Is Necessary for Canonical Wnt Signaling During Kidney Development

被引:34
作者
Karner, Courtney M. [1 ]
Merkel, Calli E. [1 ]
Dodge, Michael [2 ]
Ma, Zhiqiang [3 ]
Lu, Jianming [3 ]
Chen, Chuo [3 ]
Lum, Lawrence [2 ]
Carroll, Thomas J. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Internal Med Nephrol & Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Cell Biol, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Chem, Dallas, TX 75390 USA
关键词
Wnt; beta-catenin; tankyrase; porcupine; metanephros; kidney; development; ureteric bud; renal vesicle; BETA-CATENIN; GENE; EPITHELIUM; CANCER; MICE; MORPHOGENESIS; INACTIVATION; MESENCHYME; FIBROSIS; POLARITY;
D O I
10.1002/dvdy.22340
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Recent studies using small molecule antagonists have revealed that the poly(ADP-ribose) polymerases (PARPs) Tankyrase 1 and 2 are critical regulators of canonical Wnt signaling in some cellular contexts. However, the absence of any activity during zebrafish embryogenesis suggested that the tankyrases may not be general/core components of the Wnt pathway. Here, we show that Tnks1 and 2 are broadly expressed during mouse development and are essential during kidney and lung development. In the kidney, blockage of tankyrase activity phenocopies the effect of blocking production of all Wnt ligands. Tankyrase inhibition can be rescued by activation of beta-catenin demonstrating its specificity for the Wnt pathway. In addition, treatment with tankyrase inhibitors appears to be completely reversible in some cell types. These studies suggest that the tankyrases are core components of the canonical Wnt pathway and their inhibitors should enjoy broad usage as antagonists of Wnt signaling. Developmental Dynamics 239:2014-2023, 2010. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:2014 / 2023
页数:10
相关论文
共 34 条
[1]   Wnt signaling in polycystic kidney disease [J].
Benzing, Thomas ;
Simons, Matias ;
Walz, Gerd .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2007, 18 (05) :1389-1398
[2]   Canonical WNT/β-catenin signaling is required for ureteric branching [J].
Bridgewater, Darren ;
Cox, Brian ;
Cain, Jason ;
Lau, Agnes ;
Athaide, Valerie ;
Gill, Paul S. ;
Kuure, Satu ;
Sainio, Kirsi ;
Rosenblum, Norman D. .
DEVELOPMENTAL BIOLOGY, 2008, 317 (01) :83-94
[3]   Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system [J].
Carroll, TJ ;
Park, JS ;
Hayashi, S ;
Majumdar, A ;
McMahon, AP .
DEVELOPMENTAL CELL, 2005, 9 (02) :283-292
[4]   Small molecule-mediated disruption of Wnt-dependent signaling in tissue regeneration and cancer [J].
Chen, Baozhi ;
Dodge, Michael E. ;
Tang, Wei ;
Lu, Jianming ;
Ma, Zhiqiang ;
Fan, Chih-Wei ;
Wei, Shuguang ;
Hao, Wayne ;
Kilgore, Jessica ;
Williams, Noelle S. ;
Roth, Michael G. ;
Amatruda, James F. ;
Chen, Chuo ;
Lum, Lawrence .
NATURE CHEMICAL BIOLOGY, 2009, 5 (02) :100-107
[5]   Tankyrase 1 and Tankyrase 2 Are Essential but Redundant for Mouse Embryonic Development [J].
Chiang, Y. Jeffrey ;
Hsiao, Susan J. ;
Yver, Dena ;
Cushman, Samuel W. ;
Tessarollo, Lino ;
Smith, Susan ;
Hodes, Richard J. .
PLOS ONE, 2008, 3 (07)
[6]   Generation and characterization of telomere length maintenance in tankyrase 2-deficient mice [J].
Chiang, YJ ;
Nguyen, ML ;
Gurunathan, S ;
Kaminker, P ;
Tessarollo, L ;
Campisi, J ;
Hodes, RJ .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (06) :2037-2043
[7]   PARsing the Phrase "All in for Axin" - Wnt Pathway Targets in Cancer [J].
Fearon, Eric R. .
CANCER CELL, 2009, 16 (05) :366-368
[8]   Wnt signaling in renal cancer [J].
Guillen-Ahlers, Hector .
CURRENT DRUG TARGETS, 2008, 9 (07) :591-600
[9]   Intestinal polyposis in mice with a dominant stable mutation of the β-catenin gene [J].
Harada, N ;
Tamai, Y ;
Ishikawa, T ;
Sauer, B ;
Takaku, K ;
Oshima, M ;
Taketo, MM .
EMBO JOURNAL, 1999, 18 (21) :5931-5942
[10]   Wnt/β-Catenin Signaling Promotes Renal Interstitial Fibrosis [J].
He, Weichun ;
Dai, Chunsun ;
Li, Yingjian ;
Zeng, Gang ;
Monga, Satdarshan P. ;
Liu, Youhua .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2009, 20 (04) :765-776