Literature DB >> 2989539

Partial suppression of an ochre mutation in Saccharomyces cerevisiae by multicopy plasmids containing a normal yeast tRNAGln gene.

G A Pure, G W Robinson, L Naumovski, E C Friedberg.   

Abstract

We screened a yeast genomic library for recombinant DNA plasmids that complemented the ultraviolet (u.v.) sensitivity of a strain of Saccharomyces cerevisiae designated rad4-3 that is defective in excision repair of DNA. A multicopy plasmid (pNF4000) with a 9.4 X 10(3) base-pair yeast DNA insert partially complemented the u.v. sensitivity of rad4-3, but not of two other rad4 allelic mutants (rad4-2 and rad4-4), or of other u.v.-sensitive rad mutants. The yeast insert was analyzed by restriction mapping, DNA-DNA hybridization, DNA-tRNA hybridization and DNA sequencing. This analysis revealed the presence of a normal tRNAGln gene, a yeast sigma element situated 5' to the transfer RNA gene, a Ty element and a solo delta element. Deletion analysis of pNF4000 showed that the tRNAGln gene is required for partial complementation of the u.v. sensitivity of rad4-3. Furthermore, a multicopy plasmid containing a tRNAGln gene derived from a different region of the yeast genome also partially complemented the u.v. sensitivity of rad4-3. The rad4-3 mutation is suppressed following transformation with a plasmid containing the known ochre suppressor SUP11-o, indicating that it is an ochre mutation. We therefore conclude that when expressed in sufficient quantity, normal tRNAGln (which usually decodes the sense codon CAA) can weakly suppress the nonsense ochre codon UAA, and suggest that this represents an example of wobble occurring at the first rather than at the third position of the codon.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 2989539     DOI: 10.1016/0022-2836(85)90278-5

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  52 in total

Review 1.  Misreading of termination codons in eukaryotes by natural nonsense suppressor tRNAs.

Authors:  H Beier; M Grimm
Journal:  Nucleic Acids Res       Date:  2001-12-01       Impact factor: 16.971

2.  Identification of a tRNA(Gln) ochre suppressor in Saccharomyces cerevisiae.

Authors:  C Boone; K L Clark; G F Sprague
Journal:  Nucleic Acids Res       Date:  1992-09-11       Impact factor: 16.971

3.  Evidence of abundant stop codon readthrough in Drosophila and other metazoa.

Authors:  Irwin Jungreis; Michael F Lin; Rebecca Spokony; Clara S Chan; Nicolas Negre; Alec Victorsen; Kevin P White; Manolis Kellis
Journal:  Genome Res       Date:  2011-10-12       Impact factor: 9.043

Review 4.  Eucaryotic codes.

Authors:  F Caron
Journal:  Experientia       Date:  1990-12-01

5.  Mutational inactivation of the Saccharomyces cerevisiae RAD4 gene in Escherichia coli.

Authors:  R Fleer; W Siede; E C Friedberg
Journal:  J Bacteriol       Date:  1987-11       Impact factor: 3.490

6.  A comparative genomics analysis of codon reassignments reveals a link with mitochondrial proteome size and a mechanism of genetic code change via suppressor tRNAs.

Authors:  Steven E Massey; James R Garey
Journal:  J Mol Evol       Date:  2007-03-27       Impact factor: 2.395

7.  Bases in the anticodon loop of tRNA(Ala)(GGC) prevent misreading.

Authors:  Hiroshi Murakami; Atsushi Ohta; Hiroaki Suga
Journal:  Nat Struct Mol Biol       Date:  2009-03-22       Impact factor: 15.369

8.  Construction of an opal suppressor by oligonucleotide-directed mutagenesis of a Saccharomyces cerevisiae tRNA(Trp) gene.

Authors:  A L Atkin; K L Roy; J B Bell
Journal:  Mol Cell Biol       Date:  1990-08       Impact factor: 4.272

Review 9.  Termination of protein synthesis.

Authors:  M F Tuite; I Stansfield
Journal:  Mol Biol Rep       Date:  1994-05       Impact factor: 2.316

Review 10.  Modulation of efficiency of translation termination in Saccharomyces cerevisiae.

Authors:  Anton A Nizhnikov; Kirill S Antonets; Sergey G Inge-Vechtomov; Irina L Derkatch
Journal:  Prion       Date:  2014-11-01       Impact factor: 3.931

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.