Literature DB >> 7543481

Growth properties associated with A-U replacement of specific G-C base pairs in 16S rRNA from Escherichia coli.

K L Triman1.   

Abstract

Mutations that disrupt each of seven specific G-C base pairs in 16S rRNA from Escherichia coli confer loss of expression of a plasmid-encoded 16S rRNA selectable marker (spectinomycin resistance). However, A-U replacement of G-C base pairs at nucleotides 359/52 or 1292/1245 in 16S rRNA permits normal expression of the marker. By contrast, A-U replacements at 146/176, 153/168, 350/339, or 1293/1244 are associated with loss of expression of the marker. These genetic studies are designed to determine the importance of specific base pairs by assessment of the structural and functional impairments of 16S rRNA molecules resulting from expression of base pair substitutions at these positions.

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Year:  1995        PMID: 7543481      PMCID: PMC177204          DOI: 10.1128/jb.177.15.4514-4516.1995

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  12 in total

Review 1.  RNA-protein interactions in 30S ribosomal subunits: folding and function of 16S rRNA.

Authors:  S Stern; T Powers; L M Changchien; H F Noller
Journal:  Science       Date:  1989-05-19       Impact factor: 47.728

Review 2.  The functional role of ribosomal RNA in protein synthesis.

Authors:  A E Dahlberg
Journal:  Cell       Date:  1989-05-19       Impact factor: 41.582

3.  Dominant lethal mutations in a conserved loop in 16S rRNA.

Authors:  T Powers; H F Noller
Journal:  Proc Natl Acad Sci U S A       Date:  1990-02       Impact factor: 11.205

4.  A cold-sensitive mutation in 16S rRNA provides evidence for helical switching in ribosome assembly.

Authors:  C S Dammel; H F Noller
Journal:  Genes Dev       Date:  1993-04       Impact factor: 11.361

5.  Base changes at position 792 of Escherichia coli 16S rRNA affect assembly of 70S ribosomes.

Authors:  M Santer; E Bennett-Guerrero; S Byahatti; S Czarnecki; D O'Connell; M Meyer; J Khoury; X Cheng; I Schwartz; J McLaughlin
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

6.  Development of an efficient method for generating and screening active trypsin and trypsin variants.

Authors:  L B Evnin; C S Craik
Journal:  Ann N Y Acad Sci       Date:  1988       Impact factor: 5.691

7.  Rapid and efficient site-specific mutagenesis without phenotypic selection.

Authors:  T A Kunkel
Journal:  Proc Natl Acad Sci U S A       Date:  1985-01       Impact factor: 11.205

8.  Mutations within the decoding site of Escherichia coli 16S rRNA: growth rate impairment, lethality and intragenic suppression.

Authors:  C L Thomas; R J Gregory; G Winslow; A Muto; R A Zimmermann
Journal:  Nucleic Acids Res       Date:  1988-08-25       Impact factor: 16.971

9.  Effects of mutagenesis of a conserved base-paired site near the decoding region of Escherichia coli 16 S ribosomal RNA.

Authors:  E A De Stasio; A E Dahlberg
Journal:  J Mol Biol       Date:  1990-03-05       Impact factor: 5.469

10.  A functional pseudoknot in 16S ribosomal RNA.

Authors:  T Powers; H F Noller
Journal:  EMBO J       Date:  1991-08       Impact factor: 11.598

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  2 in total

1.  A new technique for the characterization of long-range tertiary contacts in large RNA molecules: insertion of a photolabel at a selected position in 16S rRNA within the Escherichia coli ribosome.

Authors:  P V Baranov; S S Dokudovskaya; T S Oretskaya; O A Dontsova; A A Bogdanov; R Brimacombe
Journal:  Nucleic Acids Res       Date:  1997-06-15       Impact factor: 16.971

2.  The 16S ribosomal RNA mutation database (16SMDB).

Authors:  K L Triman
Journal:  Nucleic Acids Res       Date:  1996-01-01       Impact factor: 16.971

  2 in total

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