• Title of article

    Cloning and Characterization of cDNA Encoding the Rabbit tRNA-Guanine Transglycosylase 60-Kilodalton Subunit

  • Author/Authors

    Deshpande، نويسنده , , Kathryn L. and Seubert، نويسنده , , Patricia H. and Tillman، نويسنده , , David M. and Farkas، نويسنده , , Walter R. and Katze، نويسنده , , Jon R.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی 2 سال 1996
  • Pages
    7
  • From page
    1
  • To page
    7
  • Abstract
    Eukaryotes synthesize queuosine (nucleoside Q) by the irreversible base-for-base exchange of queuine (Q base) for guanine at tRNA position 34, a reaction catalyzed by tRNA-guanine transglycosylase (TGT). The physiological role of Q remains unknown but the tRNA of tumor cells often is undermodified with respect to Q. Toward an understanding of the function of Q in normal and neoplastic cells we have isolated and characterized the cDNA for rabbit TGT. Rabbit erythrocyte TGT was reported previously to be a dimer of 60- and 43-kDa subunits (N. K. Howes and W. R. Farkas, 1978,J. Biol. Chem.253, 9082–9078). Here we present the cDNA sequence for the apparent 60-kDa subunit; it contains an open reading frame encoding a 493-residue protein. The rabbit TGT 60-kDa subunit shares significant sequence similarity with the deubiquitinating enzyme family (F. R. Papa and M. Hochstrasser, 1993,Nature366, 313–319), especially with sequence elements that include conserved Cys and His residues.
  • Keywords
    queuosine , Q nucleoside , queuine , Q base , ubiquitin-dependent proteolytic pathway , deubiquitinating enzymes
  • Journal title
    Archives of Biochemistry and Biophysics
  • Serial Year
    1996
  • Journal title
    Archives of Biochemistry and Biophysics
  • Record number

    1458286