TY - JOUR
T1 - Correspondence of yeast UAA suppressors to cloned tRNAUCASer genes
AU - Broach, James R.
AU - Friedman, Linda
AU - Sherman, Fred
N1 - Funding Information:
LVr thank MS (‘. Jlc(:ill and MS V. (iuarascio for technical assistjanw I)I, .J. Hrcakrnalln aliti Dr J. Abelson for providing cloned DNA containing tjRSAAs” pewrs: I)r R. (G&eland and MS S. Wills for providing purified tRNAS”: Dr R:. I’renskv for assist,ancr with iodinatioll procedures: Dr M. Olson for communicating results pi-ior to publication : and MS S Donaldson for assist,ance in preparation of the manuscript. This work was supported ill part 114’ United States l’uhlic Health Serrice research grants (+&I 27929 and CM 12702 from the Kational Institut,es of Health and in part t)y thi ITnited States Department of’ Energ\ (contract no. DE-ACOZ-76 EV03490) at the I’niversitv of Rochester Department Radiation Biology and Biophysics. This paper has been designated report I’K-3490-19X7.
PY - 1981/8/15
Y1 - 1981/8/15
N2 - We have analyzed the genes encoding tRNAUCASer of yeast. By hybridization analysis we have established that only three genes encode tRNAUCASer, all of which have been cloned. The DNA sequences of the coding regions of all the three genes are identical, although considerable sequence divergence exists at the 3′ and 5′ flanking regions. The suppressor locus to which each of the three cloned tRNAUCASer genes corresponds was determined by integrative transformation of yeast. A leu2- sup+ yeast strain was transformed to Leu+ with plasmids which carried the LEU2 gene of yeast and one of the DNA fragments containing a tRNAUCASer gene. Integration of the plasmid at the homologous transfer RNA locus on the chromosome introduced the LEU2 marker at the site, which could then be followed in standard genetic crosses. By this method, we have shown that the three cloned fragments correspond to the serine-inserting nonsense suppressors SUP16, SUP17 and SUP19. Finally, the SUP16 allele was recovered directly from yeast by integrating a pBR322-LEU2-sup16+ hybrid plasmid at the SUP16 locus. Appropriate digestion of genomic DNA isolated from the transformed strain permitted recovery of either the wild-type allele or the SUP16 allele on plasmids that were otherwise identical to the original transforming plasmid. This method is generally applicable to the recovery of any mutant allele of yeast for which one has DNA containing the corresponding wildtype gene.
AB - We have analyzed the genes encoding tRNAUCASer of yeast. By hybridization analysis we have established that only three genes encode tRNAUCASer, all of which have been cloned. The DNA sequences of the coding regions of all the three genes are identical, although considerable sequence divergence exists at the 3′ and 5′ flanking regions. The suppressor locus to which each of the three cloned tRNAUCASer genes corresponds was determined by integrative transformation of yeast. A leu2- sup+ yeast strain was transformed to Leu+ with plasmids which carried the LEU2 gene of yeast and one of the DNA fragments containing a tRNAUCASer gene. Integration of the plasmid at the homologous transfer RNA locus on the chromosome introduced the LEU2 marker at the site, which could then be followed in standard genetic crosses. By this method, we have shown that the three cloned fragments correspond to the serine-inserting nonsense suppressors SUP16, SUP17 and SUP19. Finally, the SUP16 allele was recovered directly from yeast by integrating a pBR322-LEU2-sup16+ hybrid plasmid at the SUP16 locus. Appropriate digestion of genomic DNA isolated from the transformed strain permitted recovery of either the wild-type allele or the SUP16 allele on plasmids that were otherwise identical to the original transforming plasmid. This method is generally applicable to the recovery of any mutant allele of yeast for which one has DNA containing the corresponding wildtype gene.
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U2 - 10.1016/0022-2836(81)90553-2
DO - 10.1016/0022-2836(81)90553-2
M3 - Article
C2 - 6795357
AN - SCOPUS:0019414012
SN - 0022-2836
VL - 150
SP - 375
EP - 387
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 3
ER -