Skip to main content
Log in

Ether-induced segmentation disturbances in Drosophila melanogaster

  • Published:
Roux's archives of developmental biology Aims and scope Submit manuscript

Summary

Drosophila embryos, exposed to ether between 1 and 4 h after oviposition, develop defects ranging from the complete lack of segmentation to isolated gaps in single segments. Between these extremes are varying extents of incomplete and abnormal segmentation. On the basis of both their temporal and spatial characteristics, five major phenotype classes may be distinguished: headless — unsegmented or incompletely segmented anteriorly; gap — interruptions of segmentation not obviously periodic; alternating segment gaps — interruptions with double segment periodicities; fused segments; and short segments — truncations with single segment periodicities. Many defects resemble known mutant phenotypes. The disturbances in segmentation are predominantly global and frequently accompanied by alterations in segment specification, such that the segments obtained show no resemblance to the normal homologues. These features, together with the distinctive spatiotemporal characteristics of the defects, all point to segmentation as a dynamic process. The regular spacing of the segments and the fact that the entire range of defects is inducible by ether are further consistent with the hypothesis that at least part of the segmentation process may consist of physicochemical reactions coordinated over the whole body. The relationship between our data and data from genetic and other analyses are briefly discussed.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Cooke J, Zeeman C (1976) A clock and wavefront model for the control of the number of repeated structures during animal morphogenesis. J Theor Biol 58:455–476

    PubMed  Google Scholar 

  • Coulter D, Wieschaus E (1986) Segmentation genes and the distributions of transcripts. Nature 321:472–474

    Google Scholar 

  • Elsdale T, Pearson M, Whitehead M (1976) Abnormalities in somite segmentation following heat-shock to Xenopus embryos. J Embryol Exp Morphol 35:625–635

    PubMed  Google Scholar 

  • Frohnhöfer HG, Lehmann R, Nüsslein-Volhard C (1986) Manipulating the anteroposterior pattern of the Drosophila embryo. J Embryol Exp Morphol [suppl] 97:169–179

    Google Scholar 

  • Gloor H (1947) Phanokopie-Versuche mit Äther an Drosophila. Rev Suisse Zool 54:637–712

    Google Scholar 

  • Goodwin BC, Skelton JL, Kirk-Bell SM (1983) Control of regeneration and morphogenesis by divalent cations in Acetabularia mediterranea. Planta 157:1–7

    Google Scholar 

  • Harding K, Rushlow C, Doyle HJ, Hoey T, Levine M (1986) Cross-regulatory interactions among pair-rule genes in Drosophila. Science 233:953–959

    PubMed  Google Scholar 

  • Ho MW (1984) Environment and heredity in development and evolution. In: Ho MW, Saunders PT (eds) Beyond neo-darwinism: an introduction to the new evolutionary paradigm. Academic Press, London, pp 267–289

    Google Scholar 

  • Ho MW, Tucker C, Keeley D, Saunders PT (1983a) Effects of successive generations of ether treatment on penetrance and expression of the bithorax phenocopy in Drosophila melanogaster. J Exp Zool 225:357–368

    Google Scholar 

  • Ho MW, Bolton E, Saunders PT (1983b) The bithorax phenocopy and pattern formation. I. Spatiotemporal characteristics of the phenocopy response. Expl Cell Biol 51:282–290

    Google Scholar 

  • Ho MW, Saunders PT, Bolton E (1983c) The bithorax phenocopy and pattern formation. II. A model of prepattern formation. Expl Cell Biol 51:291–299

    Google Scholar 

  • Jaffe LF (1979) On the centripetal course of development, the Fucus egg and self-electrophoresis. In: Language, communications and development. Dev Biol [Suppl 3] pp 83–111

  • Johnson SM, Bangham AD (1969) The action of anaesthetics on phospholipid membranes. Biochim Biophys Acta 193:92–104

    PubMed  Google Scholar 

  • Jürgens G, Wieschaus E, Nüsslein-Volhard C, Kluding H (1984) Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster. II. Zygotic loci on the third chromosome. Wilhelm Roux's Arch 193:283–295

    Google Scholar 

  • Kauffman SA, Shymko RM, Trabert K (1978) Control of sequential compartment formation in Drosophila. Science 199:259–269

    PubMed  Google Scholar 

  • Kilchherr F, Baumgartner S, Bopp D, Frei E, Noll M (1986) Isolation of the paired gene of Drosophila and its spatial expression during early embryogenesis. Nature 321:493–499

    Google Scholar 

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

    PubMed  Google Scholar 

  • Martinez-Arias A (1986) A molecular season for descriptive embryology. Trends Genet 2:146

    Google Scholar 

  • Mee J, French V (1986) Disruption of segmentation in a short germ insect embryo. II. The structure of segmental abnormalities induced by heat shock. J Embryol Exp Morphol 96:267–294

    PubMed  Google Scholar 

  • Mohler J, Wieschaus EF (1986) Dominant maternal-effect mutations of Drosophila melanogaster causing the production of double abdomen embryos. Genetics 112:803–822

    PubMed  Google Scholar 

  • North G (1986) Descartes and the fruitfly. Nature 322:404–405

    Google Scholar 

  • Nüsslein-Volhard C (1977) Genetic analysis of pattern-formation in the embryo of Drosophila melanogaster. Characterization of the maternal-effect mutant bicaudal. Wilhelm Roux's Arch 183:249–268

    Google Scholar 

  • Nüsslein-Volhard C, Wieschaus E (1980) Mutations affecting segment number and polarity in Drosophila. Nature 287:795–801

    PubMed  Google Scholar 

  • Nüsslein-Volhard C, Wieschaus E, Kluding H (1984) Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster. I. Zygotic loci on the second chromosome. Wilhelm Roux's Arch 193:267–282

    Google Scholar 

  • Sander K (1976) Specification of the basic body pattern in insect embryogenesis. Adv Insect Physiol 12:125–238

    Google Scholar 

  • Sander K (1984) Embryonic pattern formation in insects: Basic concepts and their experimental foundations. In: Malacinski GM, Bryant SV (eds) Pattern formation. Macmillan, New York, pp 245–268

    Google Scholar 

  • Saunders PT, Ho MW (1985) Primary and secondary waves in prepattern formation. J Theor Biol 114:491–504

    Google Scholar 

  • Schubiger G (1976) Adult differentiation from partial Drosophila embryos after egg ligation during stages of nuclear multiplication and cellular blastoderm. Dev Biol 50:476–488

    PubMed  Google Scholar 

  • Schüpbach T, Wieschaus E (1986) Maternal effect mutations altering the anterior-posterior pattern of the Drosophila embryo. Roux's Arch Dev Biol 195:302–317

    Google Scholar 

  • Steiner E (1976) Establishment of compartments in the developing leg imaginal discs of Drosophila melanogaster. Wilhelm Roux's Arch 180:9–30

    Google Scholar 

  • Struhl G (1983) Role of the esc gene product in ensuring the selective expression of segment-specific homeotic genes in Drosophila. J Embryol Exp Morphol 76:297–331

    PubMed  Google Scholar 

  • Turner FRS, Mahowald AP (1979) Scanning electron microscopy of Drosophila melanogaster embryogenesis: III. Formation of the head and caudal segments. Dev Biol 68:96–109

    PubMed  Google Scholar 

  • Van der Meer JM (1977) Optical clear and permanent whole mount preparations for phase-contrast microscopy of cuticular structures of insect larvae. Drosophila Inf Serv 52:160

    Google Scholar 

  • Weir MP, Kornberg T (1985) Pattern of engrailed and fushi tarazu transcripts reveal novel intermediate stages in Drosophila segmentation. Nature 318:433–445

    PubMed  Google Scholar 

  • Wieschaus E, Nüsslein-Volhard C, Jürgens G (1984) Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster. III. Zygotic loci on the X-chromosome and fourth chromosome. Wilhelm Roux's Arch 193:296–307

    Google Scholar 

  • Wieschaus E, Gehring W (1976) Clonal analysis of primordial disc cells in the early embryo of Drosophila melanogaster. Dev Biol 50:249–263

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ho, M.W., Matheson, A., Saunders, P.T. et al. Ether-induced segmentation disturbances in Drosophila melanogaster . Roux's Arch Dev Biol 196, 511–521 (1987). https://doi.org/10.1007/BF00399875

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00399875

Key words

Navigation