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Gene Review

SUP11  -  tRNA

Saccharomyces cerevisiae S288c

 
 
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High impact information on SUP11

  • In diploid strains homozygous for an ochre mutation in ade2, cells carrying no copies of the SUP11 gene are red, those carrying one copy are pink, and those carrying two or more copies are white [1].
  • A cloned ochre-suppressing form of a tRNA gene, SUP11, serves as a marker on natural and in vitro-constructed chromosomes [1].
  • The selection scheme takes advantage of the fact that the cloned ochre suppressing tRNA gene, SUP11, is lethal at high copy number and therefore causes cell death when present on an ARS plasmid that lacks a cis-acting partition function [2].
  • Temperature-sensitive arp2 mutations were created by PCR mutagenesis and selected by an ade2/SUP11 sectoring screen [3].
  • Extracts prepared from pta1-1 strains had normal pre-tRNA splicing endonuclease activity. pta1-1 was suppressed by the ochre suppressor tRNA gene SUP11, indicating that the pta1-1 mutation creates a termination codon within a protein reading frame [4].
 

Biological context of SUP11

  • We examined the correlation of the temperature sensitive and antisuppression phenotypes of maf1- Delta using a colour phenotype assay in the ade2-1 SUP11 strain [5].
  • The presence of the tRNA ochre suppressors SUP11 and SUP5 is found to induce meiosis I nondisjunction in the yeast Saccharomyces cerevisiae [6].
  • A centromere has been isolated from Candida glabrata by functional selection based on the lethality of the SUP11 gene at high copy number [7].
  • During the course of this work we developed a family of 20 Escherichia coli-yeast shuttle vectors, pUN plasmids, containing ARS1 CEN4 and a variety of selectable markers as well as the SUP11 gene which can act as a color marker in the proper background [8].
 

Associations of SUP11 with chemical compounds

  • Simultaneous amber and ochre suppression with the suppressors SUP3 and SUP11, respectively, was capable of relieving the tryptophan-requiring phenotype of strains carrying the trp5-27 allele [9].
  • One site is on chromosome VI, very close to, if not allelic with, SUP11, one of eight genes coding for a tyrosine-inserting suppressor [10].
 

Other interactions of SUP11

  • Mutation in the MAF1 gene was identified in a screen for decreased efficiency of tRNA suppressor SUP11 in the yeast Saccharomyces cerevisiae (Sc). maf1-1 mutation exerts a dual phenotypic effect: antisuppression and temperature sensitive (ts) respiratory growth [11].
  • Yeast SUP7' or SUP11 nonsense suppressors have no phenotypic expression in strains deficient in the isopentenylation of A37 in tRNA [12].
  • Individual copies of Y's were marked with SUP11 and URA3 which allowed for the selection of duplications and losses of the marked Y's. Duplications occurred by ectopic recombinational interactions between Y's at different chromosome ends as well as by unequal sister chromatid exchange [13].

References

  1. Mitotic stability of yeast chromosomes: a colony color assay that measures nondisjunction and chromosome loss. Hieter, P., Mann, C., Snyder, M., Davis, R.W. Cell (1985) [Pubmed]
  2. Functional selection and analysis of yeast centromeric DNA. Hieter, P., Pridmore, D., Hegemann, J.H., Thomas, M., Davis, R.W., Philippsen, P. Cell (1985) [Pubmed]
  3. The Saccharomyces cerevisiae actin-related protein Arp2 is involved in the actin cytoskeleton. Moreau, V., Madania, A., Martin, R.P., Winson, B. J. Cell Biol. (1996) [Pubmed]
  4. PTA1, an essential gene of Saccharomyces cerevisiae affecting pre-tRNA processing. O'Connor, J.P., Peebles, C.L. Mol. Cell. Biol. (1992) [Pubmed]
  5. Up-regulation of tRNA biosynthesis affects translational readthrough in maf1-delta mutant of Saccharomyces cerevisiae. Kwapisz, M., Smagowicz, W.J., Oficjalska, D., Hatin, I., Rousset, J.P., Zoładek, T., Boguta, M. Curr. Genet. (2002) [Pubmed]
  6. Nonrecombinant meiosis I nondisjunction in Saccharomyces cerevisiae induced by tRNA ochre suppressors. Louis, E.J., Haber, J.E. Genetics (1989) [Pubmed]
  7. Isolation of a Candida glabrata centromere and its use in construction of plasmid vectors. Kitada, K., Yamaguchi, E., Arisawa, M. Gene (1996) [Pubmed]
  8. A family of versatile centromeric vectors designed for use in the sectoring-shuffle mutagenesis assay in Saccharomyces cerevisiae. Elledge, S.J., Davis, R.W. Gene (1988) [Pubmed]
  9. Characterization of the trp5-27 allele used to monitor drug-induced mitotic gene conversion in the Saccharomyces cerevisiae tester strain D7. Ehrenhofer-Murray, A.E., Würgler, F.E., Sengstag, C. Mutagenesis (1994) [Pubmed]
  10. Genetic analysis of a transposable suppressor gene in Saccharomyces cerevisiae. Laten, H.M., Gorman, J., Webb, F., Bock, R.M. Proc. Natl. Acad. Sci. U.S.A. (1976) [Pubmed]
  11. Mutation in a new gene MAF1 affects tRNA suppressor efficiency in Saccharomyces cerevisiae. Boguta, M., Czerska, K., Zoładek, T. Gene (1997) [Pubmed]
  12. Ssb1 chaperone is a [PSI+] prion-curing factor. Chacinska, A., Szczesniak, B., Kochneva-Pervukhova, N.V., Kushnirov, V.V., Ter-Avanesyan, M.D., Boguta, M. Curr. Genet. (2001) [Pubmed]
  13. Mitotic recombination among subtelomeric Y' repeats in Saccharomyces cerevisiae. Louis, E.J., Haber, J.E. Genetics (1990) [Pubmed]
 
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