Literature DB >> 3887137

Isolation of the SUP45 omnipotent suppressor gene of Saccharomyces cerevisiae and characterization of its gene product.

H J Himmelfarb, E Maicas, J D Friesen.   

Abstract

The Saccharomyces cerevisiae SUP45+ gene has been isolated from a genomic clone library by genetic complementation of paromomycin sensitivity, which is a property of a mutant strain carrying the sup45-2 allele. This plasmid complements all phenotypes associated with the sup45-2 mutation, including nonsense suppression, temperature sensitivity, osmotic sensitivity, and paromomycin sensitivity. Genetic mapping with a URA3+-marked derivative of the complementing plasmid that was integrated into the chromosome by homologous recombination demonstrated that the complementing fragment contained the SUP45+ gene and not an unlinked suppressor. The SUP45+ gene is present as a single copy in the haploid genome and is essential for viability. In vitro translation of the hybrid-selected SUP45+ transcript yielded a protein of Mr = 54,000, which is larger than any known ribosomal protein. RNA blot hybridization analysis showed that the steady-state level of the SUP45+ transcript is less than 10% of that for ribosomal protein L3 or rp59 transcripts. When yeast cells are subjected to a mild heat shock, the synthesis rate of the SUP45+ transcript was transiently reduced, approximately in parallel with ribosomal protein transcripts. Our data suggest that the SUP45+ gene does not encode a ribosomal protein. We speculate that it codes for a translation-related function whose precise nature is not yet known.

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Year:  1985        PMID: 3887137      PMCID: PMC366786          DOI: 10.1128/mcb.5.4.816-822.1985

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  45 in total

1.  A ribosomal ambiguity mutation.

Authors:  R Rosset; L Gorini
Journal:  J Mol Biol       Date:  1969-01-14       Impact factor: 5.469

2.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

3.  Genetic mapping of nonsense suppressors in yeast.

Authors:  D C Hawthorne; R K Mortimer
Journal:  Genetics       Date:  1968-12       Impact factor: 4.562

4.  Molecular cloning and biosynthetic regulation of cry1 gene of Saccharomyces cerevisiae.

Authors:  H J Himmelfarb; A Vassarotti; J D Friesen
Journal:  Mol Gen Genet       Date:  1984

5.  Alteration of ribosomal protein S17 by mutation linked to neamine resistance in Escherichia coli. I. General properties of neaA mutants.

Authors:  A Bollen; T Cabezón; M de Wilde; R Villarroel; A Herzog
Journal:  J Mol Biol       Date:  1975-12-25       Impact factor: 5.469

6.  Ribosomal protein genes of yeast contain intervening sequences.

Authors:  G H Bollen; C M Molenaar; L H Cohen; M M van Raamsdonk-Duin; W H Mager; R J Planta
Journal:  Gene       Date:  1982-04       Impact factor: 3.688

7.  Noncoordinated transcription in the absence of protein synthesis in yeast.

Authors:  R W Shulman; C E Sripati; J R Warner
Journal:  J Biol Chem       Date:  1977-02-25       Impact factor: 5.157

8.  The presence of a defective LEU2 gene on 2 mu DNA recombinant plasmids of Saccharomyces cerevisiae is responsible for curing and high copy number.

Authors:  E Erhart; C P Hollenberg
Journal:  J Bacteriol       Date:  1983-11       Impact factor: 3.490

9.  Synergistic action of genetic and phenotypic suppression of nonsense mutations in yeast Saccharomyces cerevisiae.

Authors:  A P Surguchov; E M Pospelova; V N Smirnov
Journal:  Mol Gen Genet       Date:  1981

10.  Further characterization of recessive suppression in yeast. Isolation of the low-temperature sensitive mutant of Saccharomyces cerevisiae defective in the assembly of 60 S ribosomal subunit.

Authors:  A P Surguchov; E S Fominykch; V N Smirnov; M D Ter-Avanesyan; L N Mironova; S G Inge-Vechtomov
Journal:  Biochim Biophys Acta       Date:  1981-06-26
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  23 in total

1.  GTP hydrolysis by eRF3 facilitates stop codon decoding during eukaryotic translation termination.

Authors:  Joe Salas-Marco; David M Bedwell
Journal:  Mol Cell Biol       Date:  2004-09       Impact factor: 4.272

2.  Elongation factor EF-1 alpha gene dosage alters translational fidelity in Saccharomyces cerevisiae.

Authors:  J M Song; S Picologlou; C M Grant; M Firoozan; M F Tuite; S Liebman
Journal:  Mol Cell Biol       Date:  1989-10       Impact factor: 4.272

Review 3.  The plant translational apparatus.

Authors:  K S Browning
Journal:  Plant Mol Biol       Date:  1996-10       Impact factor: 4.076

4.  The allosuppressor gene SAL4 encodes a protein important for maintaining translational fidelity in Saccharomyces cerevisiae.

Authors:  M Crouzet; F Izgu; C M Grant; M F Tuite
Journal:  Curr Genet       Date:  1988-12       Impact factor: 3.886

5.  Isolation of omnipotent suppressors in an [eta+] yeast strain.

Authors:  J A All-Robyn; D Kelley-Geraghty; E Griffin; N Brown; S W Liebman
Journal:  Genetics       Date:  1990-03       Impact factor: 4.562

Review 6.  Errors and alternatives in reading the universal genetic code.

Authors:  J Parker
Journal:  Microbiol Rev       Date:  1989-09

7.  Increased expression of Saccharomyces cerevisiae translation elongation factor 1 alpha bypasses the lethality of a TEF5 null allele encoding elongation factor 1 beta.

Authors:  T G Kinzy; J L Woolford
Journal:  Genetics       Date:  1995-10       Impact factor: 4.562

8.  Yeast omnipotent supressor SUP1 (SUP45): nucleotide sequence of the wildtype and a mutant gene.

Authors:  P Breining; W Piepersberg
Journal:  Nucleic Acids Res       Date:  1986-07-11       Impact factor: 16.971

9.  Effects on mRNA splicing of mutations in the 3' region of the Saccharomyces cerevisiae actin intron.

Authors:  L A Fouser; J D Friesen
Journal:  Mol Cell Biol       Date:  1987-01       Impact factor: 4.272

Review 10.  Polypeptide chain termination in Saccharomyces cerevisiae.

Authors:  I Stansfield; M F Tuite
Journal:  Curr Genet       Date:  1994-05       Impact factor: 3.886

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