Literature DB >> 6188840

Effects of surrounding sequence on the suppression of nonsense codons.

J H Miller, A M Albertini.   

Abstract

Using a lacI-Z fusion system, we have determined the efficiency of suppression of nonsense codons in the I gene of Escherichia coli by assaying beta-galactosidase activity. We examined the efficiency of four amber suppressors acting on 42 different amber (UAG) codons at known positions in the I gene, and the efficiency of a UAG suppressor at 14 different UGA codons. The largest effects were found with the amber suppressor supE (Su2), which displayed efficiencies that varied over a 35-fold range, and with the UGA suppressor, which displayed a 170-fold variation in efficiency. Certain UGA sites were so poorly suppressed (less than 0.2%) by the UGA suppressor that they were not originally detected as nonsense mutations. Suppression efficiency can be correlated with the sequence on the 3' side of the codon being suppressed, and in many cases with the first base on the 3' side. In general, codons followed by A or G are well suppressed, and codons followed by U or C are poorly suppressed. There are exceptions, however, since codons followed by CUG or CUC are well suppressed. Models explaining the effect of the surrounding sequence on suppression efficiency are considered in the Discussion and in the accompanying paper.

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Year:  1983        PMID: 6188840     DOI: 10.1016/0022-2836(83)90087-6

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


  127 in total

1.  Positive and negative mutant selection in the human histone hairpin-binding protein using the yeast three-hybrid system.

Authors:  F Martin; F Michel; D Zenklusen; B Müller; D Schümperli
Journal:  Nucleic Acids Res       Date:  2000-04-01       Impact factor: 16.971

2.  One protein from two open reading frames: mechanism of a 50 nt translational bypass.

Authors:  A J Herr; R F Gesteland; J F Atkins
Journal:  EMBO J       Date:  2000-06-01       Impact factor: 11.598

3.  The efficiency of Escherichia coli selenocysteine insertion is influenced by the immediate downstream nucleotide.

Authors:  K E Sandman; C J Noren
Journal:  Nucleic Acids Res       Date:  2000-02-01       Impact factor: 16.971

4.  Dynamics and efficiency in vivo of UGA-directed selenocysteine insertion at the ribosome.

Authors:  S Suppmann; B C Persson; A Böck
Journal:  EMBO J       Date:  1999-04-15       Impact factor: 11.598

5.  Decoding of tandem quadruplets by adjacent tRNAs with eight-base anticodon loops.

Authors:  B Moore; C C Nelson; B C Persson; R F Gesteland; J F Atkins
Journal:  Nucleic Acids Res       Date:  2000-09-15       Impact factor: 16.971

6.  Revised Escherichia coli selenocysteine insertion requirements determined by in vivo screening of combinatorial libraries of SECIS variants.

Authors:  Karen E Sandman; Daniel F Tardiff; Lori A Neely; Christopher J Noren
Journal:  Nucleic Acids Res       Date:  2003-04-15       Impact factor: 16.971

7.  Single amino acid changes in AspRS reveal alternative routes for expanding its tRNA repertoire in vivo.

Authors:  Franck Martin; Sharief Barends; Gilbert Eriani
Journal:  Nucleic Acids Res       Date:  2004-08-02       Impact factor: 16.971

8.  Global transcriptional effects of a suppressor tRNA and the inactivation of the regulator frmR.

Authors:  Christopher D Herring; Frederick R Blattner
Journal:  J Bacteriol       Date:  2004-10       Impact factor: 3.490

Review 9.  Codon context.

Authors:  R H Buckingham
Journal:  Experientia       Date:  1990-12-01

10.  A simple and sensitive in vivo luciferase assay for tRNA-mediated nonsense suppression.

Authors:  D W Schultz; M Yarus
Journal:  J Bacteriol       Date:  1990-02       Impact factor: 3.490

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