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  • Castration  (1)
  • Gastrulation  (1)
  • Key words Mouse chromosome 10 and 14  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Development genes and evolution 209 (1999), S. 120-125 
    ISSN: 1432-041X
    Keywords: Key words Mouse chromosome 10 and 14 ; Maternal transcript ; Mouse Expressed Sequence Tag (EST)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  As part of a large scale mouse Expressed Sequence Tag (EST) project to identify molecules involved in the initiation of mammalian development, a homolog of the Drosophila cornichon gene was detected as a mouse maternal transcript present in the two-cell embryo. Cornichon is a multigene family in the mouse: the new gene, Cnih, maps to mouse chromosome 10, another cornichon homolog, Cnil, maps to chromosome 14 and two additional cornichon-related loci, possibly pseudogenes, localize to chromosomes 3 and 10, respectively. Cnih encodes an open reading frame (ORF) of 144 amino acids that is 93% homologous (68% identical) to the Drosophila protein, whereas the ORF of Cnil contains two extra polypeptide regions not found in these other proteins. Transcripts of Cnih are highly abundant in the full grown oocyte and the ovulated unfertilized egg, while Cnil message is only detectable after activation of the embryonic genome at the eight-cell stage. In situ hybridization shows specific localization of Cnih transcripts to ovarian oocytes. The lack of cytoplasmic polyadenylation of the maternally inherited Cnih transcript suggests that Cnih mRNA is translated in the full grown oocyte before, but not after, ovulation. In Drosophila, cornichon is involved in the establishment of both anterior-posterior and dorso-ventral polarity via the epidermal growth factor (EGF)-receptor signaling pathway. Finding Cnih in the mammalian oocyte opens a new perspective on the investigation of EGF-signaling in the oocyte.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 345 (1973), S. 295-309 
    ISSN: 1432-2013
    Keywords: Adenosinetriphosphatase ; Submaxillary Gland ; Testosterone ; Castration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The influences of castration and of testosterone administration on (NaK)-ATPase in mouse submaxillary gland has been studied. Electron microscopical and histochemical data showing a profound change in the structure of the granular tubules after castration are also presented. Whereas testosterone administration is followed by a proliferation of the rough and smooth endoplasmic reticulum in the cells of the granular tubules, castration results in an opposite change. After castration, alkaline phosphatase, which is primarily localized in the basal membranes of the granular tubules, is drastically reduced. The tissue was fractionated, by the procedure of Katz and Epstein [15], and microsomal membranes were isolated by a modification of the procedure described by Schwartzet al. [29]. Plasma membranes were isolated by the method of Henninget al. [9]. As regards MgNaK-ATPase activity in plasma membranes, castration produced a slight decrease inV max values. In the same membrane preparation, a completely opposite results was obtained for NaK-ATPase. In microsomal membranes a tremendous increase inV max with a change inK m occured when potassium chloride was varied. When sodium chloride was constant and KCl concentration varied, the same high increase inV max was recorded, but inK m the decrease was not so strongly pronounced. The conclusion was reached that the high specific activity of NaK-ATPase in castrated mouse submaxillary gland may be a consequence of a different amount of membrane protein per unit of tissue weight.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Molecular Reproduction and Development 35 (1993), S. 140-150 
    ISSN: 1040-452X
    Keywords: Gastrulation ; Germ layer ; Postimplantation ; Two-dimensional gel ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The changes in protein synthesis that occur during differentiation of the primitive germ layers were examined by high-resolution, two-dimensional gel electrophoresis of proteins synthesized in 6.5 and 7.5 days postcoitum (d.p.c.) mouse embryos. For 6.5 d.p.c. embryos, protein synthesis patterns were compared between whole extraembryonic and embryonic regions and between embryonic visceral endoderm and embryonic ectoderm. For 7.5 d.p.c. embryos, comparisons were made between extraembryonic and embryonic regions and between isolated embryonic endoderm, mesoderm, and ectoderm. Each of the isolated 7.5 d.p.c. germ layers was divided into anterior and posterior fragments in order to evaluate possible regional differences in gene expression along the anterior-posterior axis. Comparisons of protein synthesis patterns revealed the greatest difference between isolated endoderm and ectoderm, indicating that by as early as 6.5 d.p.c. patterns of gene expression differ significantly between these tissues. The greatest similarities were found between ectoderm and whole embryonic regions and between endoderm and whole extraembryonic regions, which most likely reflects the overall cellular compositions of the embryonic and extraembryonic regions. Based on their patterns of synthesis, four groups of proteins were identified that were preferentially synthesized in either endoderm or ectoderm. These provide useful markers for studying differentiation in these tissues. One other protein, migrating at the position expected for vimentin, was synthesized at an elevated rate in isolated mesoderm. We also observed differences in rates of synthesis of α-tubulin and tropomyosin-5 indicative of potential differences in cytoskeletal composition among the germ layers beyond those previously described. The difference in overall protein synthesis patterns between anterior and posterior regions was greatest in the embryonic endoderm, indicating that differentiation along the anterior-posterior axis may be initiated sooner or may proceed more rapidly in the endoderm than in the other germ layers. These data provide the first quantitative evaluation of the degree to which differentiation of the three primitive germ layers affects protein synthesis patterns and reveal potentially useful markers of endoderm and ectoderm differentiation. © 1993 Wiley-Liss, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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