Literature DB >> 1926139

The egg-shell of Drosophila melanogaster. VI, Structural analysis of the wax layer in laid eggs.

I Papassideri1, L H Margaritis, T Gulik-Krzywicki.   

Abstract

Utilizing freeze-fracturing conventional electron microscopy and scanning electron microscopy methods, a wax layer was identified, sealing the oocyte of Drosophila melanogaster. In mature egg-shells wax forms a hydrophobic layer surrounding the oocyte and lying between, and in very close contact with the vitelline membrane (interiorly) and the crystalline intermediate chorionic layer (exteriorly). In cross-fractured views it is less than 50 A thick whereas in longitudinal fracturing it reveals smooth fracture faces of a multilayered material in the form of hydrophobic areas or plaques (0.5-1 microns in diameter) which are partially overlapping and highly compressed between the vitelline membrane and the innermost chorionic layer. The evidence for this layer being a wax are the facts that a) it is not preserved in conventional fat-extracting electron microscopy methods, b) it directs laterally the fracture planes during freeze-fracturing and reveals smooth fracture faces. Analysis of the structural features of wax in mature egg-shell in various species of Drosophilidae have shown that the wax layer exhibits indistinguishable (among the species) hydrophobic plaques, which have the same size and thickness with Drosophila melanogaster. These data provide structural evidence explaining the physiological resistance of the insect eggs studied, against water loss or water uptake, whenever they are laid on substrates with extreme environmental conditions. In addition, the data demonstrate how an extracellular substance can be organized to perform that function.

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Year:  1991        PMID: 1926139     DOI: 10.1016/0040-8166(91)90014-k

Source DB:  PubMed          Journal:  Tissue Cell        ISSN: 0040-8166            Impact factor:   2.466


  4 in total

1.  Permeabilization of Drosophila embryos for introduction of small molecules.

Authors:  Matthew D Rand; Alison L Kearney; Julie Dao; Todd Clason
Journal:  Insect Biochem Mol Biol       Date:  2010-08-19       Impact factor: 4.714

2.  Palisade is required in the Drosophila ovary for assembly and function of the protective vitelline membrane.

Authors:  Maggie Elalayli; Jacklyn D Hall; Mazen Fakhouri; Hannah Neiswender; Tambrea T Ellison; Zhe Han; Penny Roon; Ellen K LeMosy
Journal:  Dev Biol       Date:  2008-05-08       Impact factor: 3.582

3.  Drosophila melanogaster cloak their eggs with pheromones, which prevents cannibalism.

Authors:  Sunitha Narasimha; Konstantin O Nagornov; Laure Menin; Antonio Mucciolo; Astrid Rohwedder; Bruno M Humbel; Martin Stevens; Andreas S Thum; Yury O Tsybin; Roshan K Vijendravarma
Journal:  PLoS Biol       Date:  2019-01-10       Impact factor: 8.029

4.  Cortical movement of Bicoid in early Drosophila embryos is actin- and microtubule-dependent and disagrees with the SDD diffusion model.

Authors:  Xiaoli Cai; Mira Akber; Alexander Spirov; Stefan Baumgartner
Journal:  PLoS One       Date:  2017-10-03       Impact factor: 3.240

  4 in total

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