Loss of ICAT gene function leads to arrest of ureteric bud branching and renal agenesis

Biochemical and Biophysical Research Communications

Volumn 362, Issue 4, 2007, Pages 988-994

  Hasegawa, Yoshimi ^a   Satoh, Kiyotoshi ^b   Iizuka Kogo, Akiko ^a   Shimomura, Atsushi ^a,c   Nomura, Ryuji ^a   Akiyama, Tetsu ^b   Senda, Takao ^a  

^a FUJITA HEALTH UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c FUJITA HEALTH UNIVERSITY   (Japan)

Author keywords

Catenin; Apoptosis; ICAT; Kidney development; Metanephric mesenchymal cells; Metanephros; Ureteric bud; Wnt signaling

Indexed keywords

BETA CATENIN; GENE PRODUCT; PROTEIN ICAT; T CELL FACTOR; UNCLASSIFIED DRUG; WNT PROTEIN;

ANIMAL CELL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CONTROLLED STUDY; EMBRYO; EMBRYO DEVELOPMENT; GENE; GENE FUNCTION; GENE LOSS; ICAT GENE; KIDNEY AGENESIS; KIDNEY DEVELOPMENT; MESENCHYME CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; SIGNAL TRANSDUCTION; URETER; WILD TYPE;

ANIMALS; CELL CYCLE PROTEINS; EMBRYONIC DEVELOPMENT; KIDNEY; MICE; MICE, KNOCKOUT; MORPHOGENESIS; TRANSCRIPTION FACTORS; URETER;

EID: 34548567438     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2007.08.085     Document Type: Article

References (31)

1. Gordon M.D., and Nusse R. Wnt signaling: multiple pathways, multiple receptors, and multiple transcription factors. J. Biol. Chem. 281 (2006) 22429-22433
2. Wang J., Etheridge L., and Boris A.W. The Wnt-signaling pathways in mammalian patterning and morphogenesis. Adv. Dev. Biol. 17 (2007) 111-158
3. Hoppler S., and Kavanagh C.L. Wnt signalling: variety at the core. J. Cell Sci. 120 (2007) 385-393
4. Tago K., Nakamura T., Nishita M., Hyodo J., Nagai S., Murata Y., Adachi S., Ohwada S., Morishita Y., Shibuya H., and Akiyama T. Inhibition of Wnt signaling by ICAT, a novel β-catenin-interacting protein. Genes Dev. 14 (2000) 1741-1749
5. Satoh K., Kasai M., Ishidao T., Tago K., Ohwada S., Hasegawa Y., Senda T., Takada S., Nada S., Nakamura T., and Akiyama T. Anteriorization of neural fate by inhibitor of β-catenin and T cell factor (ICAT), a negative regulator of Wnt signaling. Proc. Natl. Acad. Sci. USA 101 (2004) 8017-8021
6. Kuure S., Vuolteenaho R., and Vainio S. Kidney morphogenesis: cellular and molecular regulation. Mech. Dev. 92 (2000) 31-45
7. Pichel J.G., Shen L., Sheng H.Z., Granholm A.C., Drago J., Grinberg A., Lee E.J., Huang S.P., Saarma M., Hoffer B.J., Sariola H., and Westphal H. Defects in enteric innervation and kidney development in mice lacking GDNF. Nature 382 (1996) 73-76
8. Nishinakamura R., Matsumoto Y., Nakao K., Nakamura K., Sato A., Copeland N.G., Gilbert D.J., Jenkins N.A., Scully S., Lacey D.L., Katsuki M., Asashima M., and Yokota T. Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development. Development 128 (2001) 3105-3115
9. Torres M., Gómez-Pardo E., Dressler G.R., and Gruss P. Pax-2 controls multiple steps of urogenital development. Development 121 (1995) 4057-4065
10. Xu P.X., Adams J., Peters H., Brown M.C., Heaney S., and Maas R. Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia. Nat. Genet. 23 (1999) 113-117
11. Cacalano G., Fariñas I., Wang L.C., Hagler K., Forgie A., Moore M., Armanini M., Phillips H., Ryan A.M., Reichardt L.F., Hynes M., Davies A., and Rosenthal A. GFRα1 is an essential receptor component for GDNF in the developing nervous system and kidney. Neuron 21 (1998) 53-62
12. - mutant mice result from defects in ureteric bud development. Development 122 (1996) 1919-1929
13. Shah M.M., Sampogna R.V., Sakurai H., Bush K.T., and Nigam S.K. Branching morphogenesis and kidney disease. Development 131 (2004) 1449-1462
14. Miyamoto N., Yoshida M., Kuratani S., Matsuo I., and Aizawa S. Defects of urogenital development in mice lacking Emx2. Development 124 (1997) 1653-1664
15. Bouchard M. Transcriptional control of kidney development. Differentiation 72 (2004) 295-306
16. Stark K., Vainio S., Vassileva G., and McMahon A.P. Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4. Nature 372 (1994) 679-683
17. Kogo A.I., Ishidao T., Akiyama T., and Senda T. Abnormal development of urogenital organs in Dlgh1-deficient mice. Development 134 (2007) 1799-1807
18. Costantini F. Renal branching morphogenesis: concepts, questions, and recent advances. Differentiation 74 (2006) 402-421
19. Horster M.F., Braun G.S., and Huber S.M. Embryonic renal epithelia: induction, nephrogenesis, and cell differentiation. Physiol. Rev. 79 (1999) 1157-1191
20. Bard J.B. Growth and death in the developing mammalian kidney: signals, receptors and conversations. Bioessays 24 (2002) 72-82
21. Burrow C.R. Regulatory molecules in kidney development. Pediatric Nephrol. 14 (2000) 240-253
22. Lin Y., Liu A., Zhang S., Ruusunen T., Kreidberg J.A., Peltoketo H., Drummond I., and Vainio S. Induction of ureter branching as a response to Wnt-2b signaling during early kidney organogenesis. Dev. Dyn. 222 (2001) 26-39
23. Lyons J.P., Mueller U.W., Ji H., Everett C., Fang X., Hsieh J.C., Barth A.M., and McCrea P.D. Wnt-4 activates the canonical β-catenin-mediated Wnt pathway and binds Frizzled-6 CRD: functional implications of Wnt/β-catenin activity in kidney epithelial cells. Exp. Cell Res. 298 (2004) 369-387
24. Itäranta P., Lin Y., Peräsaari J., Roël G., Destrée O., and Vainio S. Wnt-6 is expressed in the ureter bud and induces kidney tubule development in vitro. Genesis 32 (2002) 259-268
25. Carroll T.J., and McMahon A.P. Secreted molecules in metanephric induction. J. Am. Soc. Nephrol. 11 (2000) S116-S119
26. Carroll T.J., Park J.S., Hayashi S., Majumdar A., and McMahon A.P. Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system. Dev. Cell 9 (2005) 283-292
27. Kispert A., Vainio S., Shen L., Rowitch D.H., and McMahon A.P. Proteoglycans are required for maintenance of Wnt-11 expression in the ureter tips. Development 122 (1996) 3627-3637
28. Majumdar A., Vainio S., Kispert A., McMahon J., and McMahon A.P. Wnt11 and Ret/Gdnf pathways cooperate in regulating ureteric branching during metanephric kidney development. Development 130 (2003) 3175-3185
29. Iglesias D.M., Hueber P.A., Chu L., Campbell R., Patenaude A.M., Dziarmaga A.J., Quinlan J., Mohamed O., Dufort D., and Goodyer P.R. Canonical WNT signaling during kidney development. Am. J. Physiol. Renal Physiol. 293 (2007) F494-F500
30. Takemaru K., Yamaguchi S., Lee Y.S., Zhang Y., Carthew R.W., and Moon R.T. Chibby, a nuclear β-catenin-associated antagonist of the Wnt/Wingless pathway. Nature 422 (2003) 905-909
31. Valenta T., Lukas J., and Korinek V. HMG box transcription factor TCF-4's interaction with CtBP1 controls the expression of the Wnt target Axin2/Conductin in human embryonic kidney cells. Nucleic Acids Res. 31 (2003) 2369-2380