Expression of the apoptosis gene reaper in homeotic, segmentation and other mutants in Drosophila

Gene Expression Patterns

Volumn 9, Issue 5, 2009, Pages 357-363

  Zhai, Zongzhao ^a,b,c   Stein, M A Sokrates ^a   Lohmann, Ingrid ^a,b  

^a MAX PLANCK INSTITUTE FOR DEVELOPMENTAL BIOLOGY   (Germany)

^b UNIVERSITY OF HEIDELBERG   (Germany)

^c INSTITUTE OF ZOOLOGY   (China)

Author keywords

Apoptosis; Hox genes; reaper; Segmentation genes; Transcriptional regulation

Indexed keywords

GENE PRODUCT; REAPER PROTEIN; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ANIMAL TISSUE; APOPTOSIS; ARTICLE; CONTROLLED STUDY; DROSOPHILA MELANOGASTER; EMBRYO; EMBRYO SEGMENTATION; EMBRYONIC STRUCTURES; GENE EXPRESSION; IN SITU HYBRIDIZATION; INSECT GENETICS; MORPHOGENESIS; MUTANT; NONHUMAN; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; TRANSCRIPTION REGULATION;

ANIMALS; APOPTOSIS; BODY PATTERNING; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; EMBRYO, NONMAMMALIAN; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HOMEODOMAIN PROTEINS; IN SITU HYBRIDIZATION; MUTATION;

DROSOPHILA MELANOGASTER; METAZOA;

EID: 67349140920     PISSN: 1567133X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.gep.2009.01.004     Document Type: Article

References (63)

1. Baehrecke E.H. How death shapes life during development. Nat. Rev. Mol. Cell Biol. 3 (2002) 779-787
2. Baumgartner S., and Noll M. Network of interactions among pair-rule genes regulating paired expression during primordial segmentation of Drosophila. Mech. Dev. 33 (1990) 1-18
3. Bhat K.M., and Schedl P. Requirement for engrailed and invected genes reveals novel regulatory interactions between engrailed/invected, patched, gooseberry and wingless during Drosophila neurogenesis. Development 124 (1997) 1675-1688
4. Boll W., and Noll M. The Drosophila Pox neuro gene: control of male courtship behavior and fertility as revealed by a complete dissection of all enhancers. Development 129 (2002) 5667-5681
5. Brodsky M.H., Nordstrom W., Tsang G., Kwan E., Rubin G.M., and Abrams J.M. Drosophila p53 binds a damage response element at the reaper locus. Cell 101 (2000) 103-113
6. Buscarlet M., and Stifani S. The 'Marx' of Groucho on development and disease. Trends Cell Biol. 17 (2007) 353-361
7. Casanova J., Sanchez-Herrero E., and Morata G. Identification and characterization of a parasegment specific regulatory element of the Abdominal-B gene of Drosophila. Cell 47 (1986) 627-636
8. Castelli-Gair J. The lines gene of Drosophila is required for specific functions of the Abdominal-B Hox protein. Development 125 (1998) 1269-1274
9. Chandrasekaran V., and Beckendorf S.K. Senseless is necessary for the survival of embryonic salivary glands in Drosophila. Development 130 (2003) 4719-4728
10. Chen P., Nordstrom W., Gish B., and Abrams J.M. Grim, a novel cell death gene in Drosophila. Genes Dev. 10 (1996) 1773-1782
11. Christich A., Kauppila S., Chen P., Sogame N., Ho S.I., and Abrams J.M. The damage-responsive Drosophila gene sickle encodes a novel IAP binding protein similar to but distinct from reaper, grim, and hid. Curr. Biol. 12 (2002) 137-140
12. Curtiss J., and Heilig J.S. Establishment of Drosophila imaginal precursor cells is controlled by the Arrowhead gene. Development 121 (1995) 3819-3828
13. Dambly-Chaudiere C., Jamet E., Burri M., Bopp D., Basler K., Hafen E., Dumont N., Spielmann P., Ghysen A., and Noll M. The paired box gene Pox neuro: a determinant of poly-innervated sense organs in Drosophila. Cell 69 (1992) 159-172
14. Fisher A.L., and Caudy M. Groucho proteins: transcriptional corepressors for specific subsets of DNA-binding transcription factors in vertebrates and invertebrates. Genes Dev. 12 (1998) 1931-1940
15. Gebelein B., McKay D.J., and Mann R.S. Direct integration of Hox and segmentation gene inputs during Drosophila development. Nature 431 (2004) 653-659
16. Ghysen A., and Dambly-Chaudiere C. From DNA to form: the Achaete-Scute complex. Genes Dev. 2 (1988) 495-501
17. Gray S., and Levine M. Transcriptional repression in development. Curr. Opin. Cell Biol. 8 (1996) 358-364
18. Grether M.E., Abrams J.M., Agapite J., White K., and Steller H. The head involution defective gene of Drosophila melanogaster functions in programmed cell death. Genes Dev. 9 (1995) 1694-1708
19. Hatini V., Green R.B., Lengyel J.A., Bray S.J., and Dinardo S. The Drumstick/Lines/Bowl regulatory pathway links antagonistic Hedgehog and Wingless signaling inputs to epidermal cell differentiation. Genes Dev. 19 (2005) 709-718
20. Heitzler P., Bourouis M., Ruel L., Carteret C., and 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. Hu N., and Castelli-Gair J. Study of the posterior spiracles of Drosophila as a model to understand the genetic and cellular mechanisms controlling morphogenesis. Dev. Biol. 214 (1999) 197-210
22. Hueber S.D., Bezdan D., Henz S.R., Blank M., Wu H., and Lohmann I. Comparative analysis of Hox downstream genes in Drosophila. Development 134 (2007) 381-392
23. Hueber S.D., and Lohmann I. Shaping segments: Hox gene function in the genomic age. Bioessays 30 (2008) 965-979
24. Hughes C.L., and Kaufman T.C. Hox genes and the evolution of the arthropod body plan. Evol. Dev. 4 (2002) 459-499
25. Ingham P.W., Baker N.E., and Martinez-Arias A. Regulation of segment polarity genes in the Drosophila blastoderm by fushi tarazu and even skipped. Nature 331 (1988) 73-75
26. Irvine K.D., and Rauskolb C. Boundaries in development: formation and function. Annu. Rev. Cell Dev. Biol. 17 (2001) 189-214
27. Iwaki D.D., Johansen K.A., Singer J.B., and Lengyel J.A. Drumstick, bowl, and lines are required for patterning and cell rearrangement in the Drosophila embryonic hindgut. Dev. Biol. 240 (2001) 611-626
28. Knust E., Tietze K., and Campos-Ortega J.A. Molecular analysis of the neurogenic locus Enhancer of split of Drosophila melanogaster. EMBO J. 6 (1987) 4113-4123
29. Kornbluth S., and White K. Apoptosis in Drosophila: neither fish nor fowl (nor man, nor worm). J. Cell Sci. 118 (2005) 1779-1787
30. Kuhnlein R.P., and Schuh R. Dual function of the region-specific homeotic gene spalt during Drosophila tracheal system development. Development 122 (1996) 2215-2223
31. Kumar S., and Cakouros D. Transcriptional control of the core cell-death machinery. Trends Biochem. Sci. 29 (2004) 193-199
32. Kuroiwa A., Kloter U., Baumgartner P., and Gehring W.J. Cloning of the homeotic Sex combs reduced gene in Drosophila and in situ localization of its transcripts. EMBO J. 4 (1985) 3757-3764
33. Langeland J.A., and Carroll S.B. Conservation of regulatory elements controlling hairy pair-rule stripe formation. Development 117 (1993) 585-596
34. Lawrence P.A., and Johnston P. Pattern formation in the Drosophila embryo: allocation of cells to parasegments by even-skipped and fushi tarazu. Development 105 (1989) 761-767
35. Lawrence P.A., Johnston P., Macdonald P., and Struhl G. Borders of parasegments in Drosophila embryos are delimited by the fushi tarazu and even-skipped genes. Nature 328 (1987) 440-442
36. Lengyel J.A., and Iwaki D.D. It takes guts: the Drosophila hindgut as a model system for organogenesis. Dev. Biol. 243 (2002) 1-19
37. Lewis E.B. A gene complex controlling segmentation in Drosophila. Nature 276 (1978) 565-570
38. Lohmann I. Dissecting the regulation of the Drosophila cell death activator reaper. Gene Expr. Patterns 3 (2003) 159-163
39. Lohmann I., McGinnis N., Bodmer M., and McGinnis W. The Drosophila Hox gene Deformed sculpts head morphology via direct regulation of the apoptosis activator reaper. Cell 110 (2002) 457-466
40. Mahaffey J.W., Griswold C.M., and Cao Q.M. The Drosophila genes disconnected and disco-related are redundant with respect to larval head development and accumulation of mRNAs from Deformed target genes. Genetics 157 (2001) 225-236
41. Mann R.S., and Morata G. The developmental and molecular biology of genes that subdivide the body of Drosophila. Annu. Rev. Cell Dev. Biol. 16 (2000) 243-271
42. McGinnis W., and Krumlauf R. Homeobox genes and axial patterning. Cell 68 (1992) 283-302
43. Miller D.F., Rogers B.T., Kalkbrenner A., Hamilton B., Holtzman S.L., and Kaufman T. Cross-regulation of Hox genes in the Drosophila melanogaster embryo. Mech. Dev. 102 (2001) 3-16
44. Mlodzik M., Fjose A., and Gehring W.J. Molecular structure and spatial expression of a homeobox gene from the labial region of the Antennapedia-complex. EMBO J. 7 (1988) 2569-2578
45. Nolo R., Abbott L.A., and Bellen H.J. Senseless, a Zn finger transcription factor, is necessary and sufficient for sensory organ development in Drosophila. Cell 102 (2000) 349-362
46. Nusslein-Volhard C., Wieschaus E., and Kluding H. Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster. I. Zygotic loci on the second chromosome. Roux Arch. Dev. Biol. 193 (1984) 267-282
47. Pazdera T.M., Janardhan P., and Minden J.S. Patterned epidermal cell death in wild-type and segment polarity mutant Drosophila embryos. Development 125 (1998) 3427-3436
48. Pearson J.C., Lemons D., and McGinnis W. Modulating Hox gene functions during animal body patterning. Nat. Rev. Genet. 6 (2005) 893-904
49. Ringrose L., and Paro R. Epigenetic regulation of cellular memory by the Polycomb and Trithorax group proteins. Annu. Rev. Genet. 38 (2004) 413-443
50. Rivera-Pomar R., and Jackle H. From gradients to stripes in Drosophila embryogenesis: filling in the gaps. Trends Genet. 12 (1996) 478-483
51. Rogers B.T., and Kaufman T.C. Structure of the insect head as revealed by the EN protein pattern in developing embryos. Development 122 (1996) 3419-3432
52. Romani S., Campuzano S., and Modolell J. The achaete-scute complex is expressed in neurogenic regions of Drosophila embryos. EMBO J. 6 (1987) 2085-2092
53. Smith S.T., and Jaynes J.B. A conserved region of Engrailed, shared among all En-, Gsc-, Nk1-, Nk2- and Msh-class homeoproteins, mediates active transcriptional repression in vivo. Development 122 (1996) 3141-3150
54. St. Johnston D., and Nusslein-Volhard C. The origin of pattern and polarity in the Drosophila embryo. Cell 68 (1992) 201-219
55. Stanewsky R., Rendahl K.G., Dill M., and Saumweber H. Genetic and molecular analysis of the X chromosomal region 14B17-14C4 in Drosophila melanogaster: loss of function in NONA, a nuclear protein common to many cell types, results in specific physiological and behavioral defects. Genetics 135 (1993) 419-442
56. Tautz D., and Pfeifle C. A non-radioactive in situ hybridization method for the localization of specific RNAs in Drosophila embryos reveals translational control of the segmentation gene hunchback. Chromosoma 98 (1989) 81-85
57. Thompson C.B. Apoptosis in the pathogenesis and treatment of disease. Science 267 (1995) 1456-1462
58. Tolkunova E.N., Fujioka M., Kobayashi M., Deka D., and Jaynes J.B. Two distinct types of repression domain in Engrailed: one interacts with the Groucho corepressor and is preferentially active on integrated target genes. Mol. Cell. Biol. 18 (1998) 2804-2814
59. Wedeen C., Harding K., and Levine M. Spatial regulation of Antennapedia and bithorax gene expression by the Polycomb locus in Drosophila. Cell 44 (1986) 739-748
60. Werz C., Lee T.V., Lee P.L., Lackey M., Bolduc C., Stein D.S., and Bergmann A. Mis-specified cells die by an active gene-directed process, and inhibition of this death results in cell fate transformation in Drosophila. Development 132 (2005) 5343-5352
61. White K., Grether M.E., Abrams J.M., Young L., Farrell K., and Steller H. Genetic control of programmed cell death in Drosophila. Science 264 (1994) 677-683
62. White K., Tahaoglu E., and Steller H. Cell killing by the Drosophila gene reaper. Science 271 (1996) 805-807
63. Zhang Y., Lin N., Carroll P.M., Chan G., Guan B., Xiao H., Yao B., Wu S.S., and Zhou L. Epigenetic blocking of an enhancer region controls irradiation-induced proapoptotic gene expression in Drosophila embryos. Dev. Cell 14 (2008) 481-493