Spatially restricted factors cooperate with Notch in the regulation of Enhancer of split genes

Developmental Biology

Volumn 221, Issue 2, 2000, Pages 390-403

  Cooper, Michael T D ^a   Tyler, David M ^a   Furriols, Marc ^a   Chalkiadaki, Angeliki ^b   Delidakis, Christos ^b   Bray, Sarah ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b UNIVERSITY OF CRETE   (Greece)

Author keywords

Drosophila; E(spl); Gene expression; Imaginal discs; Notch

Indexed keywords

NOTCH RECEPTOR;

ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DROSOPHILA HYDEI; DROSOPHILA MELANOGASTER; ENHANCER REGION; GENE EXPRESSION REGULATION; GENE FUNCTION; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; REGULATOR GENE; REGULATORY MECHANISM; SIGNAL TRANSDUCTION;

DROSOPHILA;

EID: 0034657381     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1006/dbio.2000.9691     Document Type: Article

References (59)

1. Apidianakis Y., Nagel A. C., Chalkiadaki A., Preiss A., Delidakis C. Overexpression of the m4 and mα genes of the E(spl)-complex antagonizes Notch mediated lateral inhibition. Mech. Dev. 86:1999;39-50.
2. Artavanis-Tsakonas S., Rand M. D., Lake R. J. Notch signaling: Cell fate control and signal integration in development. Science. 284:1999;770-776.
3. Bailey A. M., Posakony J. W. Suppressor of Hairless directly activates transription of Enhancer of split Complex genes in response to Notch receptor activity. Genes Dev. 9:1995;2609-2622.
4. Bienz M. TCF: Transcriptional activator or repressor? Curr. Opin. Cell Biol. 10:1998;366-372.
5. Brand A. H., Perrimon N. Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development. 118:1993;401-415.
6. Bray S. Notch signalling in Drosophila: three ways to use a pathway. Semin. Cell Dev. Biol. 9:1998;591-597.
7. Cooper M. T., Bray S. J. Frizzled regulation of Notch signalling polarizes cell fate in the Drosophila eye. Nature. 397:1999;526-530.
8. Cubas P., de Celis J. F., Campuzano S., Modolell J. Proneural clusters of achaete-scute expression and the generation of sensory organs in the Drosophila imaginal wing disc. Genes Dev. 5:1991;996-1008.
9. de Celis J. F., de Celis J., Legoxigakis P., Preiss A., Delidakis C., Bray S. Functional relationships between Notch, Su(H) and the bHLH genes of the E(spl) complex: The E(spl) genes mediate only a subset of Notch activities during imaginal development. Development. 122:1996;2719-2728.
10. Delidakis C., Artavanis-Tsakonas S. The Enhancer of split [E(spl)] locus of Drosophila encodes seven independent helix-loop-helix proteins. Proc. Natl. Acad. Sci. USA. 89:1992;8731-8735.
11. Delidakis C., Preiss A., Hartley D. A., Artavanis-Tsakonas S. Two genetically and molecularly distinct functions involved in early neurogenesis reside within the Enhancer of Split locus of Drosophila melanogaster. Genetics. 129:1991;803-823.
12. Dunin-Borkowski O. M., Brown N. H. Mammalian CD2 is an effective heterologous marker of the cell surface in Drosophila. Dev. Biol. 168:1995;689-693.
13. Eastman D. S., Slee R., Skoufos E., Bangalore L., Bray S. J., Delidakis C. Synergy between Suppressor of Hairless and Notch in the regulation of Enhancer of split mγ and mδ expression. Mol. Cell. Biol. 17:1997;5620-5628.
14. Gho M., Lecourtois M., Geraud G., Posakony J. W., Schweisguth F. Subcellular localization of Suppressor of Hairless in Drosophila sense organ cells during Notch signalling. Development. 122:1996;1673-1682.
15. Gomez-Skarmeta J. L., Rodriguez I., Martinez C., Culi J., Ferres-Marco D., Beamonte D., Modolell J. Cis-regulation of achaete and scute: Shared enhancer-like elements drive their coexpression in proneural clusters of the imaginal discs. Genes Dev. 9:1995;1869-1882.
16. Gomez-Skarmeta J. L., Modolell J. araucan and caupolican provide a link between compartment subdivisions and patterning of sensory organs and veins in the Drosophila wing. Genes Dev. 10:1996;2935-2945.
17. Gould A., Morrison A., Sproat G., White R. A. H., Krumlauf R. Positive cross-regulation and enhancer sharing: Two mechanisms for specifying overlapping Hox expression patterns. Genes Dev. 11:1997;900-913.
18. Greenwald I. LIN-12/Notch signaling: Lessons from worms and flies. Genes Dev. 12:1998;1751-1762.
19. Halder G., Polaczyk P., Kraus M. E., Hudson A., Kim J., Laughon A., Carroll S. The Vestigial and Scalloped proteins act together to directly regulate wing-specific gene expression in Drosophila. Genes Dev. 12:1998;3900-3909.
20. Heitzler P., Bourouis M., Ruel L., Carteret C., Simpson P. Genes of the Enhancer of split and achaete-scute complexes are required for a regulatory loop between Notch and Delta during lateral signalling in Drosophila. Development. 122:1996;161-171.
21. Hinz U., Giebel B., Campos-Ortega J. The basic-helix-loop-helix domain of Drosophila Lethal of Scute protein is sufficient for proneural function and activates neurogenic genes. Cell. 76:1994;77-87.
22. Hiromi Y., Kuroiwa A., Gehring W. Control elements of the Drosophila segmentation gene fushi tarazu. Cell. 43:1985;603-613.
23. Hsieh J. J., Hayward S. D. Masking of the CBF1/RBPJ kappa transcriptional repression domain by Epstein-Barr virus EBNA2. Science. 268:1995;560-563.
24. Jarriault S., Brou C., Logeat F., Schroeter E. H., Kopan R., Israel A. Signalling downstream of activated mammalian Notch. Nature. 377:1995;355-358.
25. Jennings B., de Celis J., Delidakis C., Preiss A., Bray S. Role of Notch and achaete-scute complex in the expression of Enhancer of split bHLH proteins. Development. 121:1995;3745-3752.
26. Jennings B., Preiss A., Delidakis C., Bray S. The Notch signalling pathway is required for Enhancer of split bHLH protein expression during neurogenesis in the Drosophila embryo. Development. 120:1994;3537-3548.
27. Jennings B. H., Tyler D. M., Bray S. J. Target specificities of Drosophila Enhancer of split basic helix-loop-helix proteins. Mol. Cell. Biol. 19:1999;4600-4610.
28. Jimenez G., Ish-Horowicz D. A chimeric Enhancer-of-split transcriptional activator drives neural development and achaete-scute expression. Mol. Cell. Biol. 17:1997;4355-4362.
29. Kao H. Y., Ordentlich P., Koyano-Nakagawa N., Tang Z., Downes M., Kintner C. R., Evans R. M., Kadesch T. A histone deacetylase corepressor complex regulates the Notch signal transduction pathway. Genes Dev. 12:1998;2269-2277.
30. Kim J., Sebring A., Esch J. J., Kraus M. E., Vorwerk K., Magee J., Carroll S. B. Integration of positional signals and regulation of wing formation and identity by Drosophila vestigial gene. Nature. 382:1996;133-138.
31. Knust E., Schrons H., Grawe F., Campos-Ortega J. A. Seven genes of the Enhancer of split Complex of Drosophila melanagaster encode helix-loop-helix proteins. Genetics. 132:1992;505-518.
32. Kramatschek B., Campos-Ortega J. A. Neuroectodermal transcription of the Drosophila neurogenic genes E(spl) and HLH-m5 is regulated by proneural genes. Development. 120:1994;815-826.
33. Kuroda K., Tani S., Tamura K., Minoguchi S., Kurooka H., Honjo T. Delta-induced Notch signaling mediated by RBP-J inhibits MyoD expression and myogenesis. J. Biol. Chem. 274:1999;7238-7244.
34. Lai E. C., Burks C., Posakony J. W. The K box, a conserved 3′ UTR sequence motif, negatively regulates accumulation of Enhancer of split Complex transcripts. Development. 125:1998;4077-4088.
35. Lecourtois M., Schweisguth F. The neurogenic Suppressor of Hairless DNA-binding protein mediates the transcriptional activation of the Enhancer of split Complex genes triggered by Notch signalling. Genes Dev. 9:1995;2598-2608.
36. Lecourtois M., Schweisguth F. Indirect evidence for Delta-dependent intracellular processing of Notch in Drosophila embryos. Curr. Biol. 8:1998;771-774.
37. Maier D., Marte B. M., Schafer W., Yu Y., Preiss A. Drosophila evolution challeges postulated redundancy in the E(spl) gene complex. Proc. Natl. Acad. Sci. USA. 90:1993;5464-5468.
38. Montagne J., Groppe J., Guillemin K., Krasnow M. A., Gehring W. J., Affolter M. The Drosophila Serum Response Factor gene is required for the formation of intervein tissue of the wing and is allelic to blistered. Development. 122:1996;2589-2597.
39. Nellesen D. T., Lai E. C., Posakony J. W. Discrete enhancer elements mediate selective responsiveness of Enhancer of split Complex genes to common transcriptional activators. Dev. Biol. 213:1999;33-53.
40. Neumann C. J., Cohen S. M. Boundary formation in the Drosophila wing: Notch activity attenuated by the POU protein Nubbin. Science. 281:1998;409-413.
41. Rubin G. M., Spradling A. C. Vectors for P-element mediated gene transfer in Drosophila. Nucleic Acids Res. 11:1983;6341-6351.
42. Schroeter E. H., Kisslinger J. A., Kopan R. Notch-1 signalling requires ligand-induced proteolytic release of intracellular domain. Nature. 393:1998;382-386.
43. Schrons H., Knust E., Campos-Ortega J. A. The Enhancer of split Complex and adjacent genes in the 96F regions of Drosophila melanogaster are required for segregation of neural and epidermal progenitor cells. Genetics. 132:1992;481-503.
44. Schweisguth F., Posakony J. W. Suppressor of Hairless, the Drosophila homolog of the mouse recombination signal-binding protein gene, control sensory organ cell fates. Cell. 69:1992;1199-1212.
45. Simon J. A., Sutton S. C., Lobell R. B., Glaser R. L., Lis J. T. Determinants of heat shock-induced chromosome puffing. Cell. 40:1985;805-817.
46. Singson A., Leviten M. W., Bang A. G., Xuequn H. H., Posakony J. Direct downstream targets of proneural activators in the imaginal disc include genes involved with lateral inhibitory signalling. Genes Dev. 8:1994;2058-2071.
47. Skeath J. B., Carroll S. B. Regulation of acheate-scute gene expression and sensory organ pattern formation in the Drosophila wing. Genes Dev. 5:1991;984-995.
48. Speicher S. A., Thomas U., Hinz U., Knust E. The Serrate locus of Drosophila and its role in morphogenesis of the wing imaginal discs: Control of cell proliferation. Development. 1994;535-544.
49. Staehling-Hampton K., Jackson P. D., Clark M. J., Brand A. H., Hoffmann F. M. Specificity of Bone Morphogenetic Protein-related factors: Cell fate and gene expression changes in Drosophila embryos induced by decapentaplegic but not 60A. Cell Growth Differ. 5:1994;585-593.
50. Struhl G., Adachi A. Nuclear access and action of Notch in vivo. Cell. 93:1998;649-660.
51. Struhl G., Fitzgerald K., Greenwald I. Intrinsic activity of the Lin-12 and Notch intracellular domains in vivo. Cell. 74:1993;331-345.
52. Struhl K. Fundamentally different logic of gene regulation in eukaryotes and prokaryotes. Cell. 98:1999;1-4.
53. The I., Hannigan G. E., Cowley G. S., Reginald S., Zhong Y., Gusella J. F., Hariharan I. K., Bernards A. Rescue of a Drosophila NF1 mutant phenotype by Protein Kinase A. Science. 276:1997;791-794.
54. D, a domi-nant allele of the Drosophila gene Serrate. Genetics. 120:1995;203-213.
55. Van Doren M., Powell P. A., Pasternak D., Singson A., Posakony J. Spatial regulation of proneural gene activity: Auto- and cross-activation of achaete is antagonized by extramacrochaetae. Genes Dev., 1992;2592-2605.
56. Vervoort M., Crozatier M., Valle D., Vincent A. The COE transcription factor Collier is a mediator of short-range Hedgehog-induced patterning of the Drosophila wing. Curr. Biol. 9:1999;632-639.
57. Wech I., Bray S., Delidakis C., Preiss A. Distinct expression patterns of different Enhancer of split bHLH genes during embryogenesis of Drosophila melanogaster. Dev. Genes Evol. 209:1999;370-375.
58. Wettstein D. A., Turner D. L., Kintner C. The Xenopus homolog of Drosophila Suppressor of Hairless mediates Notch signaling during primary neurogenesis. Development. 124:1997;693-702.
59. Wurmbach E., Wech I., Preiss A. The Enhancer of split Complex of Drosophila melanogaster harbors three classes of Notch responsive genes. Mech. Dev. 80:1999;171-180.