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  • Electron microscopy  (2)
  • Electrophoresis  (1)
  • Springer  (3)
  • 1975-1979  (3)
  • 1930-1934
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  • Springer  (3)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Development genes and evolution 187 (1979), S. 255-266 
    ISSN: 1432-041X
    Keywords: Yolk proteins ; Hormonal control ; Electrophoresis ; In vivo culture ; Drosophila
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Immature ovaries ofDrosophila mercatorum were injected into young larvae and into adult males ofD. mercatorum, D. melanogaster, D. hydei, D. virilis, andZaprionius vittiger. These homo- and heteroplastic transplantations allow normal vitellogenesis to occur in the donor ovary. By SDS gel electrophoresis, we identified the major species-specific yolk proteins of mature eggs (stage 14) which were exclusively of donor-specific origin. Other experiments withD. hydei andZ. vittiger showed that, when females were used as hosts, the host-specific yolk proteins became incorporated into the donor eggs. When two immature ovaries, one ofD. mercatorum and one ofD. hydei, were co-cultured in males, again only the donor-specific yolk proteins were found in the mature eggs implying that these yolk proteins were not released into the host hemolymph. A parthenogenetic strain ofD. mercatorum was used to demonstrate the ability of transplanted immature ovaries to produce viable eggs which can give rise to fertile adults. The role of the species-specific yolk proteins is discussed with respect to the dual origin of these proteins during normal vitellogenesis, i.e., an autonomous synthesis within the ovary itself in addition to the well-known production by the fat body. Further experiments with pupae as hosts indicate that even in the absence of juvenile hormone and in the presence of high doses of ecdysone, vitellogenesis can proceed within the donor ovary. Based on these experiments, a new hyopthesis on the hormonal control of vitellogenesis inDrosophila is presented. We propose that yolk proteins derived from the fat body are controlled by juvenile hormone, whereas the independent and autonomous vitellogenesis within the ovary itself is controlled by endogenously synthesized ecdysone.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0878
    Keywords: OsO4 ; Cholesterol ; Symbiotes ; Aphids ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Pea aphids left for 48 h in unbuffered osmium tetroxide show heavy staining of many organelles in the symbiote-containing cells (mycetocytes and sheath), embryos and oenocytes very similar to that characteristic of mammalian sterol-synthesizing cells. However, the staining of the pea-aphid cells is, to a large extent, dependent on the presence of cholesterol benzoate, or free cholesterol, in the aphid's diet. In aphids cultured in vitro with 3H mevalonate in the presence of added cholesterol, the incorporation of label into the cholesterol and lanosterol fractions is significantly reduced. If the dietary cholesterol effects a similar inhibition in vivo, the cholesterol-dependent osmium staining could be due to precursors(s) of cholesterol accumulating in the intracellular sites described. There is also osmium staining of large (normally electron-transparent) vacuoles in mycetocytes, gut and fat body, irrespective of dietary cholesterol.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 159 (1975), S. 351-367 
    ISSN: 1432-0878
    Keywords: Symbiotes ; Aphids ; Vesicles ; Organelles ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A detailed investigation into the ultrastructure of the pea aphid mycetocytes and their contained symbiotes and organelles was carried out with the transmission electron microscope. The most striking observation was the presence of small vesicles in the space between the primary symbiote cell wall and membrane envelope (outer membrane space). The vesicles appear to form by a budding process at the outer cell wall layer. Subsequently, the vesicles, we suggest, may move out into the mycetocyte cytoplasm via a similar budding of the membrane envelope. The Golgi apparatus was found to be an important structural component of the primary mycetocyte; it is continuous with the rough endoplasmic reticulum and the latter, in turn, appears to be closely connected to the primary symbiote membrane envelope. This may be of functional significance. A number of other organelles not previously described in mycetocytes were found, including transparent vacuoles, granular bodies, multivesicular bodies and microfilaments. The chemical composition of the various vesicles and organelles is unknown at present.
    Type of Medium: Electronic Resource
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