Literature DB >> 7828587

The identity of the base following the stop codon determines the efficiency of in vivo translational termination in Escherichia coli.

E S Poole1, C M Brown, W P Tate.   

Abstract

A statistical analysis of > 2000 Escherichia coli genes suggested that the base following the translational stop codon might be an important feature of the signal for termination. The strengths of each of 12 possible 'four base stop signals' (UAAN, UGAN and UAGN) were tested in an in vivo termination assay that measured termination efficiency by its direct competition with frameshifting. Termination efficiencies varied significantly depending on both the stop codon and the fourth base, ranging from 80 (UAAU) to 7% (UGAC). For both the UAAN and UGAN series, the fourth base hierarchy was U > G > A approximately C. UAG stop codons, which are used rarely in E. coli, showed efficiencies comparable with UAAN and UGAN, but differed in that the hierarchy of the fourth base was G > U approximately A > C. The rate of release factor selection varied 30-fold at UGAN stop signals, and 10-fold for both the UAAN and UAGN series; it correlated well with the frequency with which the different UAAN and UGAN signals are found at natural termination sites. The results suggest that the identity of the base following the stop codon determines the efficiency of translational termination in E. coli. They also provide a rationale for the use of the strong UAAU signal in highly expressed genes and for the occurrence of the weaker UGAC signal at several recording sites.

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Year:  1995        PMID: 7828587      PMCID: PMC398062          DOI: 10.1002/j.1460-2075.1995.tb06985.x

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  50 in total

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6.  Mitochondrial phosphate transport. Large scale isolation and characterization of the phosphate transport protein from beef heart mitochondria.

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7.  Conditionally lethal and recessive UGA-suppressor mutations in the prfB gene encoding peptide chain release factor 2 of Escherichia coli.

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8.  The effect of codon usage on the oligonucleotide composition of the E. coli genome and identification of over- and underrepresented sequences by Markov chain analysis.

Authors:  G J Phillips; J Arnold; R Ivarie
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Review 9.  Selenocysteine: the 21st amino acid.

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10.  Reading frame switch caused by base-pair formation between the 3' end of 16S rRNA and the mRNA during elongation of protein synthesis in Escherichia coli.

Authors:  R B Weiss; D M Dunn; A E Dahlberg; J F Atkins; R F Gesteland
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  85 in total

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Journal:  RNA       Date:  2000-12       Impact factor: 4.942

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7.  A dynamic competition between release factor 2 and the tRNA(Sec) decoding UGA at the recoding site of Escherichia coli formate dehydrogenase H.

Authors:  J B Mansell; D Guévremont; E S Poole; W P Tate
Journal:  EMBO J       Date:  2001-12-17       Impact factor: 11.598

8.  The C-terminal amino acid sequence of nascent peptide is a major determinant of SsrA tagging at all three stop codons.

Authors:  Takafumi Sunohara; Tatsuhiko Abo; Toshifumi Inada; Hiroji Aiba
Journal:  RNA       Date:  2002-11       Impact factor: 4.942

9.  Chicken MAR-binding protein ARBP is homologous to rat methyl-CpG-binding protein MeCP2.

Authors:  J M Weitzel; H Buhrmester; W H Strätling
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10.  Cis control of gene expression in E.coli by ribosome queuing at an inefficient translational stop signal.

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Journal:  EMBO J       Date:  2002-08-15       Impact factor: 11.598

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