Literature DB >> 6774986

The eggshell of Drosophila melanogaster. I. Fine structure of the layers and regions of the wild-type eggshell.

L H Margaritis, F C Kafatos, W H Petri.   

Abstract

The fine structure of the several layers and regional specializations in the Drosophila melanogaster eggshell has been studied by a combination of shell isolation procedures and ultrastructural techniques (conventional TEM, whole-mount TEM, SEM, HVEM, freeze-fracture electron microscopy utilizing rotary replication, shadow casting, optical diffraction and stereo imaging). The main shell consists of 5 layers: the vitelline membrane (300 nm thick), the wax layer, the innermost chorionic layer (40-50 nm), the endochorion (500-700 nm), and the exochorion (300-500 nm). The vitelline membrane consists of irregularly organized particles. The wax layer appears to contain multilayered hydrophobic plates which split tangenitally upon freeze fracturing. The innermost chorionic layer is composed of a crystalling lattice. The endochorion is made of a thin (40 nm) fenestrated floor composed of 40-nm fibres and an outer solid (200 nm) roof covered with a network of 40-nm strands. Intermittently spaced pillar connect these 2 parts. Similarities in the substructure of the floor, pillars and roof suggest that they may be composed of similar or identical structural elements. The specialized regions of the shell are the 2 respiratory appendages, the operculum area and the posterior pole. The appendages exhibit 2 sharply distinct surfaces, a dorsal side with isolated 1.5-micrometer plaques and a ventral side with strands of 40-50 nm connected in a network with openings of 70-80 nm. The operculum area, which includes the micropoyle and the collar, is distinguished by 3 unique types of cell imprints. The posterior pole contains 2 distinctive populations of cell imprints: the central area has very thin intercellular ridges and a thin, perforated, endochorionic roof, while the peripheral area contains mixed, thick and thin, intercellular ridges and serves as a transition zone to the main shell pattern. The pillars in the central area of the posterior pole have a distinct arrangement, forming one peripheral circle within each cell imprint. An analysis utilizing structural and developmental criteria indicates that as many as ten different populations of follicular epithelial cells may be involved in the construction of the various regions of the Drosophila eggshell.

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Year:  1980        PMID: 6774986     DOI: 10.1242/jcs.43.1.1

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  45 in total

1.  Chorion gene cis-regulatory DNA restricts tissue specificity of reporter gene expression in transformed Drosophila.

Authors:  B Bienz-Tadmor; P Tolias; B Stebbins-Boaz; B D Mariani; S A Gerbi; F C Kafatos
Journal:  Chromosoma       Date:  1992-08       Impact factor: 4.316

2.  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

3.  Evolutionary changes in the expression pattern of a developmentally essential gene in three Drosophila species.

Authors:  D Wang; J L Marsh; F J Ayala
Journal:  Proc Natl Acad Sci U S A       Date:  1996-07-09       Impact factor: 11.205

4.  Minor proteins and enzymes of the Drosophila eggshell matrix.

Authors:  Mazen Fakhouri; Maggie Elalayli; Daniel Sherling; Jacklyn D Hall; Eric Miller; Xutong Sun; Lance Wells; Ellen K LeMosy
Journal:  Dev Biol       Date:  2006-03-03       Impact factor: 3.582

5.  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

6.  Stage-specific localization of the small heat shock protein Hsp27 during oogenesis in Drosophila melanogaster.

Authors:  R Marin; R M Tanguay
Journal:  Chromosoma       Date:  1996-09       Impact factor: 4.316

7.  Germline and somatic vitelline proteins colocalize in aggregates in the follicular epithelium of Drosophila ovaries.

Authors:  Marc Furriols; Jordi Casanova
Journal:  Fly (Austin)       Date:  2014       Impact factor: 2.160

8.  Quantitative proteomics reveals the dynamics of protein changes during Drosophila oocyte maturation and the oocyte-to-embryo transition.

Authors:  Iva Kronja; Zachary J Whitfield; Bingbing Yuan; Kristina Dzeyk; Joanna Kirkpatrick; Jeroen Krijgsveld; Terry L Orr-Weaver
Journal:  Proc Natl Acad Sci U S A       Date:  2014-10-27       Impact factor: 11.205

9.  Trans-acting amplification mutants and other eggshell mutants of the third chromosome in Drosophila melanogaster.

Authors:  P B Snyder; V K Galanopoulos; F C Kafatos
Journal:  Proc Natl Acad Sci U S A       Date:  1986-05       Impact factor: 11.205

10.  Female sterile mutations on the second chromosome of Drosophila melanogaster. II. Mutations blocking oogenesis or altering egg morphology.

Authors:  T Schüpbach; E Wieschaus
Journal:  Genetics       Date:  1991-12       Impact factor: 4.562

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