APC mutant zebrafish uncover a changing temporal requirement for wnt signaling in liver development

Developmental Biology

Volumn 320, Issue 1, 2008, Pages 161-174

  Goessling, Wolfram ^a,b   North, Trista E ^a   Lord, Allegra M ^a   Ceol, Craig ^a   Lee, Sang ^a   Weidinger, Gilbert ^c   Bourque, Caitlin ^a   Strijbosch, Robbert ^a   Haramis, Anna Pavlina ^d   Puder, Mark ^a   Clevers, Hans ^e   Moon, Randall T ^f   Zon, Leonard I ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b MASSACHUSETTS GENERAL HOSPITAL   (United States)

^c DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

^d NETHERLANDS CANCER INSTITUTE   (Netherlands)

^e HUBRECHT INSTITUTE   (Netherlands)

^f UNIVERSITY OF WASHINGTON   (United States)

Author keywords

APC; Endoderm; Liver; Regeneration; wnt; Zebrafish; catenin

Indexed keywords

APC; WNT PROTEIN;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BLASTULA; CELL PROLIFERATION; CONTROLLED STUDY; EMBRYO; GENE EXPRESSION; GENE LOSS; GENE MUTATION; HEPATOBLASTOMA; LIVER DEVELOPMENT; LIVER REGENERATION; MORPHOGENESIS; MUTANT; NONHUMAN; PRIORITY JOURNAL; ZEBRA FISH;

DANIO RERIO; MUS; VERTEBRATA;

EID: 47649084257     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ydbio.2008.05.526     Document Type: Article

References (55)

1. Akimenko M.A., et al. Differential induction of four msx homeobox genes during fin development and regeneration in zebrafish. Development 121 (1995) 347-357
2. Alonso L., and Fuchs E. Stem cells in the skin: waste not, Wnt not. Genes Dev. 17 (2003) 1189-1200
3. Apte U., et al. Beta-Catenin is critical for early postnatal liver growth. Am. J. Physiol.: Gastrointest. Liver Physiol. 292 (2007) G1578-G1585
4. Chazaud C., and Rossant J. Disruption of early proximodistal patterning and AVE formation in Apc mutants. Development 133 (2006) 3379-3387
5. Chenn A., and Walsh C.A. Regulation of cerebral cortical size by control of cell cycle exit in neural precursors. Science 297 (2002) 365-369
6. Christian J.L., and Moon R.T. Interactions between Xwnt-8 and Spemann organizer signaling pathways generate dorsoventral pattern in the embryonic mesoderm of Xenopus. Genes Dev. 7 (1993) 13-28
7. Clevers H. Wnt/beta-catenin signaling in development and disease. Cell 127 (2006) 469-480
8. Dequeant M.L., et al. A complex oscillating network of signaling genes underlies the mouse segmentation clock. Science 314 (2006) 1595-1598
9. Deutsch G., et al. A bipotential precursor population for pancreas and liver within the embryonic endoderm. Development 128 (2001) 871-881
10. Dorsky R.I., et al. A transgenic Lef1/beta-catenin-dependent reporter is expressed in spatially restricted domains throughout zebrafish development. Dev. Biol. 241 (2002) 229-237
11. Field H.A., et al. Formation of the digestive system in zebrafish. I. Liver morphogenesis. Dev. Biol. 253 (2003) 279-290
12. Goessling W., et al. Ultrasound biomicroscopy permits in vivo characterization of zebrafish liver tumors. Nat. Methods 4 (2007) 551-553
13. Greene A.K., and Puder M. Partial hepatectomy in the mouse: technique and perioperative management. J. Invest. Surg. 16 (2003) 99-102
14. Haegel H., et al. Lack of beta-catenin affects mouse development at gastrulation. Development 121 (1995) 3529-3537
15. Haramis A.P., et al. Adenomatous polyposis coli-deficient zebrafish are susceptible to digestive tract neoplasia. EMBO Rep. 7 (2006) 444-449
16. Heasman J., et al. Beta-catenin signaling activity dissected in the early Xenopus embryo: a novel antisense approach. Dev. Biol. 222 (2000) 124-134
17. Her G.M., et al. In vivo studies of liver-type fatty acid binding protein (L-FABP) gene expression in liver of transgenic zebrafish (Danio rerio). FEBS Lett. 538 (2003) 125-133
18. Hirschman B.A., et al. The spectrum of APC mutations in children with hepatoblastoma from familial adenomatous polyposis kindreds. J. Pediatr. 147 (2005) 263-266
19. Hurlstone A.F., et al. The Wnt/beta-catenin pathway regulates cardiac valve formation. Nature 425 (2003) 633-637
20. Ireland H., et al. Inducible Cre-mediated control of gene expression in the murine gastrointestinal tract: effect of loss of beta-catenin. Gastroenterology 126 (2004) 1236-1246
21. Kielman M.F., et al. Apc modulates embryonic stem-cell differentiation by controlling the dosage of beta-catenin signaling. Nat. Genet. 32 (2002) 594-605
22. Kinzler K.W., et al. Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers. Science 251 (1991) 1366-1370
23. Kirstetter P., et al. Activation of the canonical Wnt pathway leads to loss of hematopoietic stem cell repopulation and multilineage differentiation block. Nat. Immunol. 7 (2006) 1048-1056
24. Lewis J.L., et al. Reiterated Wnt signaling during zebrafish neural crest development. Development 131 (2004) 1299-1308
25. Lin R., et al. Pop-1 encodes an HMG box protein required for the specification of a mesoderm precursor in early C. elegans embryos. Cell 83 (1995) 599-609
26. Lyman Gingerich J., et al. Hecate, a zebrafish maternal effect gene, affects dorsal organizer induction and intracellular calcium transient frequency. Dev. Biol. 286 (2005) 427-439
27. Manisastry S.M., et al. Early temporal-specific responses and differential sensitivity to lithium and Wnt-3A exposure during heart development. Dev. Dyn. 235 (2006) 2160-2174
28. McLin V.A., et al. Repression of Wnt/{beta}-catenin signaling in the anterior endoderm is essential for liver and pancreas development. Development 134 (2007) 2207-2217
29. Micsenyi A., et al. Beta-catenin is temporally regulated during normal liver development. Gastroenterology 126 (2004) 1134-1146
30. Monga S.P., et al. Changes in WNT/beta-catenin pathway during regulated growth in rat liver regeneration. Hepatology 33 (2001) 1098-1109
31. Monga S.P., et al. Beta-catenin antisense studies in embryonic liver cultures: role in proliferation, apoptosis, and lineage specification. Gastroenterology 124 (2003) 202-216
32. Moser A.R., et al. Homozygosity for the Min allele of Apc results in disruption of mouse development prior to gastrulation. Dev. Dyn. 203 (1995) 422-433
33. Nadauld L.D., et al. Dual roles for adenomatous polyposis coli in regulating retinoic acid biosynthesis and Wnt during ocular development. Proc. Natl. Acad. Sci. U. S. A. 103 (2006) 13409-13414
34. Ober E.A., et al. From endoderm formation to liver and pancreas development in zebrafish. Mech. Dev. 120 (2003) 5-18
35. Ober E.A., et al. Mesodermal Wnt2b signalling positively regulates liver specification. Nature 442 (2006) 688-691
36. Pinto D., et al. Canonical Wnt signals are essential for homeostasis of the intestinal epithelium. Genes Dev. 17 (2003) 1709-1713
37. Pisharath H., et al. Targeted ablation of beta cells in the embryonic zebrafish pancreas using E. coli nitroreductase. Mech. Dev. 124 (2007) 218-229
38. Reya T., et al. A role for Wnt signalling in self-renewal of haematopoietic stem cells. Nature 423 (2003) 409-414
39. Sadler K.C., et al. Liver growth in the embryo and during liver regeneration in zebrafish requires the cell cycle regulator, uhrf1. Proc. Natl. Acad. Sci. U. S. A. 104 (2007) 1570-1575
40. Sansom O.J., et al. Loss of Apc in vivo immediately perturbs Wnt signaling, differentiation, and migration. Genes Dev. 18 (2004) 1385-1390
41. Sekine S., et al. Liver-specific loss of beta-catenin results in delayed hepatocyte proliferation after partial hepatectomy. Hepatology 45 (2007) 361-368
42. Sodhi D., et al. Morpholino oligonucleotide-triggered beta-catenin knockdown compromises normal liver regeneration. J. Hepatol. 43 (2005) 132-141
43. Stainier D.Y. A glimpse into the molecular entrails of endoderm formation. Genes Dev. 16 (2002) 893-907
44. Stanger B.Z., et al. Organ size is limited by the number of embryonic progenitor cells in the pancreas but not the liver. Nature 445 (2007) 886-891
45. Stoick-Cooper C.L., et al. Distinct Wnt signaling pathways have opposing roles in appendage regeneration. Development 134 (2007) 479-489
46. Su L.K., et al. Multiple intestinal neoplasia caused by a mutation in the murine homolog of the APC gene. Science 256 (1992) 668-670
47. Suksaweang S., et al. Morphogenesis of chicken liver: identification of localized growth zones and the role of beta-catenin/Wnt in size regulation. Dev. Biol. 266 (2004) 109-122
48. Tan X., et al. Conditional deletion of beta-catenin reveals its role in liver growth and regeneration. Gastroenterology 131 (2006) 1561-1572
49. Taniguchi K., et al. Mutational spectrum of beta-catenin, AXIN1, and AXIN2 in hepatocellular carcinomas and hepatoblastomas. Oncogene 21 (2002) 4863-4871
50. Tokumoto N., et al. Immunohistochemical and mutational analyses of Wnt signaling components and target genes in intrahepatic cholangiocarcinomas. Int. J. Oncol. 27 (2005) 973-980
51. Trowbridge J.J., et al. Glycogen synthase kinase-3 is an in vivo regulator of hematopoietic stem cell repopulation. Nat. Med. 12 (2006) 89-98
52. Wallace K.N., and Pack M. Unique and conserved aspects of gut development in zebrafish. Dev. Biol. 255 (2003) 12-29
53. Warga R.M., and Nusslein-Volhard C. Origin and development of the zebrafish endoderm. Development 126 (1999) 827-838
54. Weidinger G., et al. The Sp1-related transcription factors sp5 and sp5-like act downstream of Wnt/beta-catenin signaling in mesoderm and neuroectoderm patterning. Curr. Biol. 15 (2005) 489-500
55. Zorn A.M., and Wells J.M. Molecular basis of vertebrate endoderm development. Int. Rev. Cytol. 259 (2007) 49-111