Literature DB >> 7017349

A novel form of suppression due to an altered RNA polymerase.

E Ephrati-Elizur, S Luther-Davies.   

Abstract

A group of mutants isolated from E coli K12(tif-1) display a very pleiotropic phenotype. The main characteristic of these mutants, temporarily designated 'S' strains, is their ability to suppress a large number of mutations. High efficiency of suppression is correlated with increased thermolability of cellular proteins, indicating an impairment in the fidelity of protein synthesis. Efficient suppression is also accompanied by the appearance of new characteristics like simultaneous resistance to several antibiotic drugs (Sm, Spc, and Mer), and plasmid-like DNA circles. Genetic studies show that the suppressor character is located in the rpoBC region. In a large number of spontaneous Rifr mutants, isolated from these strains, suppression or resistance to drugs is lost. The findings suggest that the phenotype of 'S' strains is due to an altered RNA polymerase causing erroneous transcription.

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Year:  1981        PMID: 7017349     DOI: 10.1007/bf00425617

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  22 in total

1.  On the fidelity of transcription by Escherichia coli ribonucleic acid polymerase.

Authors:  C F Springgate; L A Loeb
Journal:  J Mol Biol       Date:  1975-10-05       Impact factor: 5.469

2.  Progressive decrease in protein synthesis accuracy induced by streptomycin in Escherichia coli.

Authors:  E W Branscomb; D J Galas
Journal:  Nature       Date:  1975-03-13       Impact factor: 49.962

3.  A quantitative assay for bacterial RNA polymerases.

Authors:  M J Chamberlin; W C Nierman; J Wiggs; N Neff
Journal:  J Biol Chem       Date:  1979-10-25       Impact factor: 5.157

4.  Reversal of mutant phenotypes by 5-fluorouracil: an approach to nucleotide sequences in messenger-RNA.

Authors:  S P CHAMPE; S BENZER
Journal:  Proc Natl Acad Sci U S A       Date:  1962-04-15       Impact factor: 11.205

5.  Transformation of Salmonella typhimurium by plasmid deoxyribonucleic acid.

Authors:  E M Lederberg; S N Cohen
Journal:  J Bacteriol       Date:  1974-09       Impact factor: 3.490

6.  X-ray inactivation of the Escherichia coli deoxyribonucleic acid dependent ribonucleic acid polymerase in aqueous solution. II. Studies on initiation and fidelity of transcription.

Authors:  G F Strniste; D A Smith; F N Hayes
Journal:  Biochemistry       Date:  1973-02       Impact factor: 3.162

7.  Restriction, de-restriction and mistranslation in missense suppression. Ribosomal discrimination of transfer RNA's.

Authors:  D K Biswas; L Gorini
Journal:  J Mol Biol       Date:  1972-02-28       Impact factor: 5.469

8.  Ribonucleic acid polymerase reactions with methylated polycytidylic acid templates.

Authors:  D B Ludlum; R C Wilhelm
Journal:  J Biol Chem       Date:  1968-05-25       Impact factor: 5.157

9.  A simple method for the preparation of large quantities of pure plasmid DNA.

Authors:  G O Humphreys; G A Willshaw; E S Anderson
Journal:  Biochim Biophys Acta       Date:  1975-04-02

10.  A possible mechanism responsible for the correction of transcription errors.

Authors:  V Z Volloch; S Rits; L Tumerman
Journal:  Nucleic Acids Res       Date:  1979-04       Impact factor: 16.971

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  2 in total

1.  Transient reversal of RNA polymerase II active site closing controls fidelity of transcription elongation.

Authors:  Maria L Kireeva; Yuri A Nedialkov; Gina H Cremona; Yuri A Purtov; Lucyna Lubkowska; Francisco Malagon; Zachary F Burton; Jeffrey N Strathern; Mikhail Kashlev
Journal:  Mol Cell       Date:  2008-06-06       Impact factor: 17.970

2.  Genetic studies on the beta subunit of Escherichia coli RNA polymerase. I. The effect of known, single amino acid substitutions in an essential protein.

Authors:  V Nene; R E Glass
Journal:  Mol Gen Genet       Date:  1982
  2 in total

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