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  • 29.30.Dn  (1)
  • Chloramphenicol resistance  (1)
  • HAP1, HAP2 transcription factors  (1)
  • Springer  (3)
  • AMER GEOPHYSICAL UNION
  • American Institute of Physics (AIP)
  • Cambridge University Press
  • ZBW - Deutsche Zentralbibliothek für Wirtschaftswissenschaften, Leibniz-Informationszentrum Wirtschaft Kiel, Hamburg
Collection
Keywords
Publisher
  • Springer  (3)
  • AMER GEOPHYSICAL UNION
  • American Institute of Physics (AIP)
  • Cambridge University Press
  • ZBW - Deutsche Zentralbibliothek für Wirtschaftswissenschaften, Leibniz-Informationszentrum Wirtschaft Kiel, Hamburg
Years
  • 1
    Electronic Resource
    Electronic Resource
    Mutation of a highly conserved base in the yeast mitochondrial 21S rRNA restricts ribosomal frameshifting (1995)
    Springer
    Molecular genetics and genomics 248 (1995), S. 207-216 
    Details
    ISSN: 1617-4623
    Keywords: Chloramphenicol resistance ; frameshifting Mitochondria ; 21S rRNA ; Yeast
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A mutation shown to cause resistance to chloramphenicol inSaccharomyces cerevisiae was mapped to the central loop in domain V of the yeast mitochondrial 21S rRNA. The mutant 21S rRNA has a base pair exchange from U2677 (corresponding to U2504 inEscherichia coli) to C2677, which significantly reduces rightward frameshifting at a UU UUU UCC A site in a + 1 U mutant. There is evidence to suggest that this reduction also applies to leftward frameshifting at the same site in a − 1 U mutant. The mutation did not increase the rate of misreading of a number of mitochondrial missense, nonsense or frameshift (of both signs) mutations, and did not adversely affect the synthesis of wild-type mitochondrial gene products. It is suggested here that ribosomes bearing either the C2677 mutation or its wild-type allele may behave identically during normal decoding and only differ at sites where a ribosomal stall, by permitting non-standard decoding, differentially affects the normal interaction of tRNAs with the chloramphenicol resistant domain V. Chloramphenicol-resistant mutations mapping at two other sites in domain V are described. These mutations had no effect on frameshifting.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02190802
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  • 2
    Electronic Resource
    Electronic Resource
    Expression of yeast cytochrome C1 is controlled at the transcriptional level by glucose, oxygen and haem (1992)
    Springer
    Molecular genetics and genomics 232 (1992), S. 447-459 
    Details
    ISSN: 1617-4623
    Keywords: Saccharomyces cerevisiae ; Cytochrome c 1 ; Promoter dissection ; HAP1, HAP2 transcription factors ; Centromere and promoter-binding factor (CPF1)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The nuclear gene for cytochrome c 1 in Saccharomyces cerevisiae (CYT1) was localized on chromosome XV. Its upstream region was identified by functional complementation. Fusion to the lacZ reporter gene on a CEN plasmid allowed study of the effect of carbon sources and of specific deletion mutations on expression of the gene in yeast transformants. Detailed promoter analysis combined with expression studies in recipient strains defective in regulatory genes identified cis-acting sites and transcription factors involved in the regulated expression of the cytochrome c 1 gene. These analyses showed that, in the presence of glucose, transcription of CYT1 is positively controlled by oxygen, presumably through the haem signal, and mediated by the HAP1-encoded transactivator. It is additionally regulated by the HAP2/3/4 complex which mediates gene activation mainly under glucose-free conditions. Basal transcription is, in part, effected by CPF1, a centromere and promoter-binding factor.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00266250
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  • 3
    Electronic Resource
    Electronic Resource
    Precision measurement of the conversion electron spectrum of83m Kr with a solenoid retarding spectrometer (1992)
    Springer
    The European physical journal 342 (1992), S. 71-78 
    Details
    ISSN: 1434-601X
    Keywords: 27.50.+e ; 29.30.Dn
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract This paper reports on precision measurements of conversion lines in the decay of83mKr with nuclear transition energies of 32.1 keV and 9.4 keV, respectively. The spectra were taken from a submonolayer surface of83m Kr frozen onto a cold backing, using the new Mainz solenoid retarding spectrometer. The high luminosity and resolution of this instrument enables the observation of all allowed conversion lines up to theN-shell and to fully separate the elastic component from inelastic satellites. The combined analysis of the data yields the transition energiesE y=32151.5±1.1 eV and 9405.9±0.8 eV, respectively. The experiment served also to pilot the application of this spectrometer to the question of a finite neutrino rest mass, searched for in theβ-decay spectrum of tritium and to problems in precision electron spectroscopy in general.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01294491
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