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  • 1985-1989  (2)
  • Storage protein  (1)
  • Sulfate  (1)
  • 11C-amino acids
  • General Chemistry
  • pharmacokinetic parameters
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 208 (1987), S. 107-113 
    ISSN: 1617-4623
    Keywords: Glycinin mutant ; Storage protein ; DNA sequence
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A null allele for the Gy 4 glycinin gene from the cultivar Raiden was sequenced and compared with a functional Gy 4 gene from another cultivar. The results showed that the null phenotype probably resulted from a point mutation that changed the translation initiation codon from ATG to ATA. Transcripts of the mutant gene were detected in total RNA from seed, but the mRNAs did not become associated with polysomes as did functional Gy 4 meassage in the control cultivar. This was probably due to premature dissociation of mutant gy 4 mRNA from ribosomes due to nonsense codons during translation of an incorrect reading frame.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0736-0266
    Keywords: Sulfate ; Cartilage ; Glycosaminoglycans ; Mouse ; Articular ; Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: We have studied the effect of environmental sulfate concentration on the glycosaminoglycan synthesis of anatomically intact patellar cartilage of the mouse in vitro. Incubation of mouse patellae in medium with sulfate concentrations below 0.5 mM resulted in a diminished incorporation of sulfate but in unaltered incorporation of glucosamine. This suggested the synthesis of undersulfated glycosaminoglycans under these conditions. We characterized glycosaminoglycans synthesized at three different sulfate concentrations: a sulfate concentration physiological for the mouse (1.0 mM), a sulfate concentration in the range where sulfate incorporation was strongly diminished (0.1 mM), and an extremely low sulfate concentration (10 nM). Analysis of glycosaminoglycan disaccharides and DEAE anion chromatography of the glycosaminoglycans could not confirm the synthesis of undersulfated glycosaminoglycans at 0.1 mM. The chromatogram of glycosaminoglycans synthesized in medium containing 10 nM showed the presence of a very low sulfated glycosaminoglycan pool not observed at higher medium sulfate concentrations. Intermediately sulfated glycosaminoglycans were also synthesized during incubation with 10 nM sulfate. So, our data indicate that only very low sulfate concentrations in the medium lead to the synthesis of undersulfated glycosaminoglycans and that the sulfation mechanism of murine patellar cartilage chondrocytes does not seem to fit completely in an “all-or-nothing” pattern.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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