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Developmental analysis of fs(1)gastrulation defective, a dorsal-group gene of Drosophila melanogaster

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Summary

The gastrulation defective (gd) locus is a maternally expressed gene in Drosophila required for normal differentiation of structures along the embryonic dorso-ventral axis. Cuticular defects of the offspring from females with different combinations of gd alleles comprised a phenotypic continuum. Complementation among several alleles produced normal offspring while progressively more severe mutations produced a graded loss of structures from ventral, and then lateral, blastoderm cells. The most severely affected embryos consisted entirely of structures derived from dorsal blastoderm cells. Histological examination of staged siblings from selected allelic combinations showed that internal tissues were similarly affected. The tissues observed in amorphic embryos support new, more dorsal, assignments of fate map positions for blastoderm precursors of the cephalopharyngeal apparatus, hindgut and ventral nerve cord. The loss of ventral and lateral structures did not occur through cell death and appeared to involve a change in blastoderm cell fate. A direct effect of the mutations on blastoderm cell determination, however, was insufficient to explain the development of the dorsalized embryos. Intermediate phenotypes suggested that cell interactions or movements associated with morphogenesis are required for the determination of some cell fates in the dorsoventral axis. Thus, the developmental fate of all blastoderm cells may not be fixed at the time of blastoderm formation.

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References

  • Anderson KV, Nüsslein-Volhard C (1984a) Genetic analysis of dorsal-ventral embryonic pattern in Drosophila. In: Malacinski G, Bryant S (eds) Primers in developmental biology. Macmillan, New York, pp 269–289

    Google Scholar 

  • Anderson KV, Nüsslein-Volhard C (1984b) Information for the dorsal-ventral pattern of the Drosophila embryo is stored as maternal mRNA. Nature 311:223–227

    Google Scholar 

  • Anderson KV, Jurgens G, Nüsslein-Volhard C (1985) The establishment of dorsal-ventral polarity in the Drosophila embryo: genetic studies on the role of the Toll gene product. Cell 42:779–789

    Google Scholar 

  • Campos-Ortega JA (1983) Topological specificity of phenotype expression of neurogenic mutations in Drosophila. Wilhelm Roux's Arch 192:317–326

    Google Scholar 

  • Campos-Ortega JA, Hartenstein V (1986) Development of Drosophila melanogaster. Springer, Berlin Heidelberg New York Tokyo

    Google Scholar 

  • Dennell RE, Frederick RD (1983) Homoeosis in Drosophila: A description of the polycomb lethal syndrome. Dev Biol 97:34–47

    Google Scholar 

  • Fullilove SL, Jacobson AG (1978) Embryonic development: Descriptive, In: Ashburner M, Wright TRF (eds) The genetics and biology of Drosophila, vol 2C. Academic Press, New York, pp 105–227

    Google Scholar 

  • Gans M, Audit C, Masson M (1975) Isolation and characterization of sex-linked female sterile mutants in Drosophila melanogaster. Genetics 81:683–704

    Google Scholar 

  • Gergen P, Wieschaus EH (1985) The localized requirements for a gene affecting segmentation in Drosophila: analysis of larvae mosaic for runt. Dev Biol 109:321–335

    Google Scholar 

  • Hall JC, Kankle DR (1976) Genetics of acetylcholinesterase in Drosophila melanogaster. Genetics 83:517–535

    Google Scholar 

  • Hartenstein V, Campos-Ortega JA (1985) Fate-mapping in wildtype Drosophila melanogaster. I. The spatio-temporal pattern of embryonic cell divisions. Wilhelm Roux's Arch 194:181–195

    Google Scholar 

  • Hartenstein V, Technau GM, Campos-Ortega JA (1985) Fate-mapping in wildtype Drosophila melanogaster. III. A fate map of the blastoderm. Wilhelm Roux's Arch 194:213–216

    Google Scholar 

  • Hoppe PE, Greenspan RJ (1986) Local function of the Notch gene for embryonic ectodermal pathway choice in Drosophila. Cell 46:773–783

    Google Scholar 

  • Kalt MR, Tandler B (1971) A study of fixation of early amphibian embryos for electron microscopy. Ultrastruct Res 36:633–645

    Google Scholar 

  • Karnovsky MJ, Roots L (1964) A “direct-coloring” thiocholine method for cholinesterase. J Histochem Cytochem 12:219–221

    Google Scholar 

  • Konrad KD, Mahowald AP (1983) Genetic and developmental approaches to understanding determination in early development. In: Malacinski G, Klein WH (eds) Molecular aspects of early development. Plenum Press, New York, pp 167–188

    Google Scholar 

  • Konrad KD, Engstrom L, Perrimon N, Mahowal AP (1985) Genetic analysis of oogenesis and the role of maternal gene expression in early development. In: Browder LW (ed) Developmental biology, vol 1. Plenum Press, New York, pp 577–617

    Google Scholar 

  • Lindsley DL, Grell EH (1968) Genetic variations of Drosophila melanogaster, Publication 627. Carnegie Institute Washington DC

    Google Scholar 

  • Lindsley DL, Zimm G (1985) The genome of Drosophila melanogaster. Drosophila Information Serv 62:188

    Google Scholar 

  • Lohs-Schardin M, Cremer C, Nüsslein-Volhard C (1979) A fate map for the larval epidermis of Drosophila melanogaster: Localized cuticle defects following irradiation of the blastoderm with an ultraviolet laser microbeam. Dev Biol 73:239–255

    Google Scholar 

  • Mahowald AP (1963) Ultrastructural differentiations during formation of the blastoderm in the Drosophila melanogaster embryo. Dev Biol 8:186–204

    Google Scholar 

  • Meinhardt H (1977) A model for pattern formation in insect embryogenesis. J Cell Sci 23:117–139

    Google Scholar 

  • Mohler JD (1977) Developmental genetics of the Drosophila egg: I. Identification of 59 sex-linked cistrons with maternal effects on embryonic development. Genetics 85:259–272

    Google Scholar 

  • Naidet C, Semeriva M, Yamada K, Thiery JP (1987) Peptides containing the cell-attachment recognition signal Agg-Gly-Asp prevent gastrulation in Drosophila embryos. Nature 325:348–350

    Google Scholar 

  • Nüsslein-Volhard C (1979) Maternal effect mutations that alter the spatial coordinates of the embryos of Drosophila melanogaster. In: Subtelny S, Königsberg IR (eds) Determinates of spatial organization. Academic Press, New York, pp 185–211

    Google Scholar 

  • Nüsslein-Volhard C, Lohs-Schardin M, Sander K, Cremer C (1980) A dorso-ventral shift of embryonic primordia in a new maternal-effect mutant of Drosophila. Nature 283:474–476

    Google Scholar 

  • Odell GM, Oster G, Alberch P, Burnside B (1981) The mechanical basis of morphogenesis. Dev Biol 85:446–462

    Google Scholar 

  • Poulson DF (1950) Histogenesis, organogenesis, and differentiation in the embryo of Drosophila melanogaster Meigen. In: Demerec M (ed) Biology of Drosophila. Wiley, New York, pp 168–274

    Google Scholar 

  • Smith DS (1968) Insect cells their structure and function. Oliver and Boyd, Edinburgh

    Google Scholar 

  • Technau GM, Campos-Ortega JA (1985) Fate mapping in wildtype Drosophila melanogaster. II. Injections of horseradish peroxidase in cells of the early gastrula stage, Wilhelm Roux's Arch 194:196–212

    Google Scholar 

  • Technau GM, Campos-Ortega JA (1986) Lineage analysis of transplanted individual cells in embryos of Drosophila melanogaster II. Commitment and proliferative capabilities of neural and epidermal cell progenitors, Wilhelm Roux's Arch 195:445–454

    Google Scholar 

  • Turner FR, Mahowald AP (1977) Scanning electron microscopy of Drosophila melanogaster embryogenesis II. Gastrulation and segmentation. Dev Biol 57:403–416

    Google Scholar 

  • Underwood EM, Turner FR, Mahowald AP (1980) Analysis of cell movements and fate mapping during embryogenesis in Drosophila melanogaster. Dev Biol 74:286–301

    Google Scholar 

  • Van der Meer J (1977) Optical clean and permanent wholemount preparation for phase contrast microscopy of cuticular structures of insect larvae. Drosophila Inform Serv 52:160

    Google Scholar 

  • Zalokar M, Erk I (1977) Phase-partition fixation and staining of Drosophila eggs. Stain Technol 52:89–95

    Google Scholar 

  • Zalokar M, Audit C, Erk I (1975) Developmental defects of female-sterile mutants of Drosophila melanogaster. Dev Biol 47:419–432

    Google Scholar 

Download references

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Konrad, K.D., Goralski, T.J. & Mahowald, A.P. Developmental analysis of fs(1)gastrulation defective, a dorsal-group gene of Drosophila melanogaster . Roux's Arch Dev Biol 197, 75–91 (1988). https://doi.org/10.1007/BF00375930

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  • DOI: https://doi.org/10.1007/BF00375930

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