Endoderm induction in Drosophila: The nuclear targets of the inducing signals

Current Opinion in Genetics and Development

Volumn 7, Issue 5, 1997, Pages 683-688

  Bienz, Mariann ^a  

^a MRC LABORATORY OF MOLECULAR BIOLOGY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CELL DIFFERENTIATION; CELL NUCLEUS; CELL TYPE; DROSOPHILA; EMBRYO; EMBRYO DEVELOPMENT; ENDODERM; MIDGUT; NONHUMAN; PRIORITY JOURNAL; SHORT SURVEY; SIGNAL TRANSDUCTION; TRANSCRIPTION REGULATION;

EID: 0030784883     PISSN: 0959437X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0959-437X(97)80017-2     Document Type: Note

References (41)

1. Gurdon JB. Embryonic induction - molecular prospects. Development. 87:1987;285-306.
2. Wessels NK. Benjamin WA. Tissue Interaction and Development. 1977;Menlo Park, New York.
3. Zaret KS. Molecular genetics of early liver development. Ann Rev Physiol. 58:1996;231-251.
4. Sengel P. Epidermal - dermal interaction. Bereiter-Hahn J, Matoltsy AG, Richards KS. The Biology of the Integument 2. Vertebrates. 1986;374-408 Springer Verlag, Berlin.
5. Thesleff I, Vaahtokari A, Partanen A. Regulation of organogenesis. Common molecular mechanisms regulating the development of teeth and other organs. Int J Dev Biol. 39:1995;35-50.
6. Haffen K, Kedinger M, Simon-Assmann P. Messenchyme-dependent differentiation of epithelial progenitor cells in the gut. J Pediat Gastroenterol Nutr. 6:1987;14-23.
7. Roberts DJ, Johnson RL, Burke AC, Nelson CE, Morgan BA, Tabin C. Sonic hedgehog is an endodermal signal inducing Bmp-4 and Hox genes during induction and regionalization of the chick hindgut. Development. 121:1995;3163-3174.
8. Bienz M. Induction of the endoderm in Drosophila. Semin Cell Dev Biol. 7:1996;113-119.
9. Immerglück K, Lawrence PA, Bienz M. Induction across germ layers in Drosophila, mediated by a genetic cascade. Cell. 62:1990;261-268.
10. Panganiban GEF, Reuter R, Scott MP, Hoffmann FM. A Drosophila growth factor homolog, decapentaplegic, regulates homeotic gene expression within and across germ layers during midgut morphogenesis. Development. 110:1990;1041-1050.
11. Reuter R, Panganiban GEF, Hoffmann FM, Scott MP. Homeotic genes regulate the spatial expression of putative growth factors in the visceral mesoderm of Drosophila embryos. Development. 110:1990;1031-1040.
12. Hoppler S, Bienz M. Specification of a single cell type by a Drosophila homeotic gene. Cell. 76:1994;689-702.
13. Hoppler S, Bienz M. Two different thresholds of wingless signalling with distinct developmental consequences in the Drosophila midgut. EMBO J. 14:1995;5016-5026.
14. Skaer H. The alimentary canal. Bate M, Martinez-Arias A. The Development of Drosophila melanogaster. 1993;941-1012 Cold Spring Harbor Laboratory Press, Cold Spring Harbor.
15. Thüringer F, Bienz M. Indirect autoregulation of a homeotic Drosophila gene mediated by extracellular signaling. Proc Natl Acad Sci USA. 90:1993;3899-3903.
16. Hursh DA, Padgett RW, Gelbart WM. Cross regulation of decapentaplegic and Ultrabithorax transcription in the embryonic visceral mesoderm of Drosophila. Development. 117:1993;1211-1222.
17. Yu X, Hoppler S, Eresh S, Bienz M. decapentaplegic, a target gene of the wingless signalling pathway in the Drosophila midgut. Development. 122:1996;849-858.
18. Niswander L, Jeffrey S, Martin GR, Tickle C. A positive feedback loop coordinates growth and patterning in the vertebrate limb. Nature. 371:1994;609-612.
19. Tada M, O'Reilly M-AJ, Smith J. Analysis of competence and of Brachyury autoinduction by use of hormone-inducible Xbra. Development. 124:1997;2225-2234.
20. Riese J, Yu X, Munnerlyn A, Eresh S, Hsu S-C, Grosschedl R, Bienz M. LEF-1, a nuclear factor coordinating signaling inputs from wingless and decapentaplegic. Cell. 88:1997;777-787.
21. Van de Wetering M, Cavallo R, Dooijes D, van Beest M, van Es J, Loureiro J, Ypma A, Hursh D, Jones T, Bejsovec A, et al. Armadillo coactivates transcription driven by the product of the Drosophila segment polarity gene dTCF. Cell. 88:1997;789-799.
22. Brunner E, Peter O, Schweizer L, Basler K. pangolin encodes a Lef-1 homologue that acts downstream of Armadillo to transduce the Wingless signal in Drosophila. Nature. 385:1997;829-833.
23. Grosschedl R, Giese K, Pagel J. HMG domain proteins: architectural elements in the assembly of nucleoprotein structures. Trends Genet. 10:1994;94-100.
24. Behrens J, von Kies JP, Kühl M, Bruhn L, Wedlich D, Grosschedl R, Birchmeier W. Functional interaction of β-catenin with the transcription factor LEF-1. Nature. 382:1996;638-642.
25. Molenaar M, van de Wetering M, Oosterwegel M, Peterson-Maduro J, Godsave S, Korinek V, Roose J, Destrée O, Clevers H. XTcf-3 transcription factor mediates β-catenin-axis formation in Xenopus embryos. Cell. 86:1996;391-399.
26. Huber O, Korn R, McLaughlin J, Ohsugi M, Herrmann BG, Kemler R. Nuclear localization of β-catenin by interaction with transcription factor LEF-1. Mech Dev. 59:1996;3-10.
27. Nusse R. A versatile transcriptional effector of Wingless signaling. Cell. 89:1997;321-323.
28. Giese K, Grosschedl R. LEF-1 contains an activation domain that stimulates transcription only in a specific context of factor-binding sites. EMBO J. 12:1993;4667-4676.
29. Carlsson P, Waterman ML, Jones KA. The hLEF/TCF-1α HMG protein contains a context-dependent transcriptional activation domain that induces the TCRα enhacer in T cells. Genes Dev. 7:1993;2418-2430.
30. Mayall TP, Sheridan PL, Montminy MR, Jones KA. Distinct roles for P-CREB and LEF-1 in TCRα enhancer assembly and activation on chromatin in vitro. Genes Dev. 11:1997;887-899.
31. Giese K, Cox J, Grosschedl R. The HMG domain of lymphoid enhancer factor 1 bends DNA and facilitates assembly of functional nucleoprotein structures. Cell. 69:1992;185-195.
32. Eresh S, Riese J, Jackson DB, Bohmann D, Bienz M. A CREB binding site as target for decapentaplegic signalling during Drosophila endoderm induction. EMBO J. 16:1997;2014-2022.
33. Montminy MR, Sevarino KA, Wagner JA, Mandel G, Goodman RH. Identification of a cyclic-AMP-responsive element within the rat somatostatin gene. Proc Natl Acad Sci USA. 83:1986;6682-6686.
34. Sassone-Corsi P. Goals for signal transduction pathways: linking up with transcriptional regulation. EMBO J. 13:1994;4717-4728.
35. Massagué J, Hata A, Liu F. TGF-β signalling through the Smad pathway. Trends Cell Biol. 7:1997;187-192.
36. Arora K, Dai H, Kazuko SG, Jamal J, O'Connor MB, Letsou A, Warrior R. The Drosophila schnurri gene acts in the Dpp/TGFβ signaling pathway and encodes a transcription factor homologous to the human MBP family. Cell. 81:1995;781-790.
37. Grieder NC, Nellen D, Burke R, Basler K, Affolter M. Schnurri is required for Drosophila Dpp signaling and encodes a zinc finger protein similar to the mammalian transcription factor PRDII-BF1. Cell. 81:1995;791-800.
38. Riese J, Tremml G, Bienz M. D-Fos, a target gene for Decapentaplegic signalling with a critical role during Drosophila endoderm induction. Development. 127:1997;3353-3361.
39. Perkins KK, Admon A, Patel N, Tijan R. The Drosophila Fos-related AP-1 protein is a developmentally regulated transcription factor. Genes Dev. 4:1990;822-834.
40. Van Genderen C, Okamura RM, Farinas I, Quo RG, Parslow TG, Bruhn L, Grosschedl R. Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1-deficient mice. Genes Dev. 8:1994;2691-2703.
41. Kratochwil K, Maude D, Farinas I, Galceran J, Grosschedl R. Lef1 expression is activated by BMP-4 and regulates inductive tissue interactions in tooth and hair development. Genes Dev. 10:1996;1382-1394.