Literature DB >> 2788746

Translation of phage f1 gene VII occurs from an inherently defective initiation site made functional by coupling.

M Ivey-Hoyle1, D A Steege.   

Abstract

Expression of the filamentous phage f1 gene VII is shown to be translationally coupled to that of the upstream gene V. Fusions of the gene VII initiation site to the lacZ coding region were used to determine that initiation at the VII site is completely dependent on the process of translation having proceeded up to a stop codon immediately upstream from the VII site. Coupled expression from the VII site was found to be inefficient, proportional to the level of upstream translation, and very sensitive to the distance from the functional upstream stop codon. Independent expression from the VII site was not observed, even in a deletion series designed to remove potentially masking RNA structure. On the basis of the VII site's dissimilarity to ribosome binding site sequences and its properties overall, we suggest that it inherently lacks the features required for independent recognition by ribosomes, and acquires the ability to initiate synthesis of gene VII protein by virtue of the coupling process.

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Year:  1989        PMID: 2788746     DOI: 10.1016/0022-2836(89)90385-9

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


  16 in total

1.  Role of ribosome recycling factor (RRF) in translational coupling.

Authors:  Y Inokuchi; A Hirashima; Y Sekine; L Janosi; A Kaji
Journal:  EMBO J       Date:  2000-07-17       Impact factor: 11.598

2.  Restoration of a translational stop-start overlap reinstates translational coupling in a mutant trpB'-trpA gene pair of the Escherichia coli tryptophan operon.

Authors:  A Das; C Yanofsky
Journal:  Nucleic Acids Res       Date:  1989-11-25       Impact factor: 16.971

3.  Distinctive patterns of translational reinitiation in the lac repressor mRNA: bridging of long distances by out-of-frame translation and RNA secondary structure, effects of primary sequence.

Authors:  R J Matteson; S J Biswas; D A Steege
Journal:  Nucleic Acids Res       Date:  1991-07-11       Impact factor: 16.971

4.  Gene V protein-mediated translational regulation of the synthesis of gene II protein of the filamentous bacteriophage M13: a dispensable function of the filamentous-phage genome.

Authors:  G J Zaman; A M Kaan; J G Schoenmakers; R N Konings
Journal:  J Bacteriol       Date:  1992-01       Impact factor: 3.490

5.  Translational coupling by modulation of feedback repression in the IF3 operon of Escherichia coli.

Authors:  C Chiaruttini; M Milet; M Springer
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-19       Impact factor: 11.205

6.  The use of two-cistron constructions in improving the expression of a heterologous gene in E. coli.

Authors:  A J Makoff; A E Smallwood
Journal:  Nucleic Acids Res       Date:  1990-04-11       Impact factor: 16.971

7.  Translational coupling and limited degradation of a polycistronic messenger modulate differential gene expression in the parD stability system of plasmid R1.

Authors:  M J Ruiz-Echevarría; G de la Cueva; R Díaz-Orejas
Journal:  Mol Gen Genet       Date:  1995-09-20

8.  Characterization of the tol-pal region of Escherichia coli K-12: translational control of tolR expression by TolQ and identification of a new open reading frame downstream of pal encoding a periplasmic protein.

Authors:  A Vianney; M M Muller; T Clavel; J C Lazzaroni; R Portalier; R E Webster
Journal:  J Bacteriol       Date:  1996-07       Impact factor: 3.490

9.  Efficiency and frequency of translational coupling between the bacteriophage T4 clamp loader genes.

Authors:  M Y Torgov; D M Janzen; M K Reddy
Journal:  J Bacteriol       Date:  1998-09       Impact factor: 3.490

Review 10.  Posttranscriptional control of gene expression in yeast.

Authors:  J E McCarthy
Journal:  Microbiol Mol Biol Rev       Date:  1998-12       Impact factor: 11.056

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