Literature DB >> 2523380

Genetic analysis of bacteriophage lambda cIII gene: mRNA structural requirements for translation initiation.

D Kornitzer1, D Teff, S Altuvia, A B Oppenheim.   

Abstract

The bacteriophage lambda cIII gene product regulates the lysogenic pathway. The cIII gene is located in the leftward operon, which is transcribed from the pL promoter. We have previously shown (S. Altuvia and A. B. Oppenheim, J. Bacteriol. 167:415-419, 1986) that mutations that show elevated expression lie within the cIII coding sequence. We isolated mutants that show decreased CIII activity. All the mutations were found to cause a drastic reduction in the rate of initiation of cIII translation. Several mutations were found to be scattered within the first 40 nucleotides of the cIII coding region. Additional mutations affected the AUG initiation codon, the Shine-Dalgarno sequence, and the upstream RNaseIII processing site. Computer folding of the cIII mRNA suggested the presence of two alternative RNA structures. All the mutations within the coding region that reduce expression reduce the stability of one specific mRNA structure (structure B). Mutations that increase expression lie in the loops of this structure and may in fact stabilize it by interfering with the formation of the alternative structure (structure A). Thus, it appears that a specific mRNA secondary structure at the beginning of the cIII coding region is essential for efficient translation, suggesting that changes in mRNA structure regulate cIII expression.

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Year:  1989        PMID: 2523380      PMCID: PMC209935          DOI: 10.1128/jb.171.5.2563-2572.1989

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


  39 in total

1.  Isolation, characterization and deletion mapping of amber mutations in the cll gene of phage lambda.

Authors:  M Belfort; D Noff; A B Oppenheim
Journal:  Virology       Date:  1975-01       Impact factor: 3.616

2.  Control of bacteriophage lambda repressor synthesis after phage infection: the role of the N, cII, cIII and cro products.

Authors:  L F Reichardt
Journal:  J Mol Biol       Date:  1975-04-05       Impact factor: 5.469

3.  Isolation and characterization of mutations in the cIII gene of bacteriophage lambda which increase the efficiency of lysogenization of Escherichia coli K-12.

Authors:  B J Knoll
Journal:  Virology       Date:  1979-01-30       Impact factor: 3.616

4.  Transcription termination sites in the major leftward operon of coliphage lambda.

Authors:  J S Salstrom; W Szybalski
Journal:  Virology       Date:  1978-07-15       Impact factor: 3.616

5.  Transcription antitermination by bacteriophage lambda N gene product.

Authors:  M E Gottesman; S Adhya; A Das
Journal:  J Mol Biol       Date:  1980-06-15       Impact factor: 5.469

Review 6.  The lysis-lysogeny decision of phage lambda: explicit programming and responsiveness.

Authors:  I Herskowitz; D Hagen
Journal:  Annu Rev Genet       Date:  1980       Impact factor: 16.830

7.  Synthesis, assembly into the cytoplasmic membrane, and proteolytic processing of the precursor of coliphage M13 coat protein.

Authors:  K Ito; T Date; W Wickner
Journal:  J Biol Chem       Date:  1980-03-10       Impact factor: 5.157

8.  Secondary structure of mRNA and efficiency of translation initiation.

Authors:  D Iserentant; W Fiers
Journal:  Gene       Date:  1980-04       Impact factor: 3.688

9.  Mutagenesis of plasmid DNA with hydroxylamine: isolation of mutants of multi-copy plasmids.

Authors:  G O Humphreys; G A Willshaw; H R Smith; E S Anderson
Journal:  Mol Gen Genet       Date:  1976-04-23

10.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

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  10 in total

1.  Autogenous regulation of the RNA polymerase beta subunit of Escherichia coli occurs at the translational level in vivo.

Authors:  L Passador; T Linn
Journal:  J Bacteriol       Date:  1989-11       Impact factor: 3.490

2.  The Escherichia coli OxyS regulatory RNA represses fhlA translation by blocking ribosome binding.

Authors:  S Altuvia; A Zhang; L Argaman; A Tiwari; G Storz
Journal:  EMBO J       Date:  1998-10-15       Impact factor: 11.598

3.  The HflB protease of Escherichia coli degrades its inhibitor lambda cIII.

Authors:  C Herman; D Thévenet; R D'Ari; P Bouloc
Journal:  J Bacteriol       Date:  1997-01       Impact factor: 3.490

4.  Proteolysis of bacteriophage lambda CII by Escherichia coli FtsH (HflB).

Authors:  Y Shotland; A Shifrin; T Ziv; D Teff; S Koby; O Kobiler; A B Oppenheim
Journal:  J Bacteriol       Date:  2000-06       Impact factor: 3.490

5.  Molecular and genetic analysis of a region of plasmid pCF10 containing positive control genes and structural genes encoding surface proteins involved in pheromone-inducible conjugation in Enterococcus faecalis.

Authors:  S M Kao; S B Olmsted; A S Viksnins; J C Gallo; G M Dunny
Journal:  J Bacteriol       Date:  1991-12       Impact factor: 3.490

6.  Genetic analysis of the cIII gene of bacteriophage HK022.

Authors:  D Kornitzer; S Altuvia; A B Oppenheim
Journal:  J Bacteriol       Date:  1991-01       Impact factor: 3.490

7.  The activity of the CIII regulator of lambdoid bacteriophages resides within a 24-amino acid protein domain.

Authors:  D Kornitzer; S Altuvia; A B Oppenheim
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-15       Impact factor: 11.205

8.  Studies on Escherichia coli HflKC suggest the presence of an unidentified λ factor that influences the lysis-lysogeny switch.

Authors:  Kaustav Bandyopadhyay; Pabitra K Parua; Ajit B Datta; Pradeep Parrack
Journal:  BMC Microbiol       Date:  2011-02-17       Impact factor: 3.605

9.  Escherichia coli FtsH is a membrane-bound, ATP-dependent protease which degrades the heat-shock transcription factor sigma 32.

Authors:  T Tomoyasu; J Gamer; B Bukau; M Kanemori; H Mori; A J Rutman; A B Oppenheim; T Yura; K Yamanaka; H Niki
Journal:  EMBO J       Date:  1995-06-01       Impact factor: 11.598

10.  Haloferax volcanii, a prokaryotic species that does not use the Shine Dalgarno mechanism for translation initiation at 5'-UTRs.

Authors:  Piet Kramer; Katrin Gäbel; Friedhelm Pfeiffer; Jörg Soppa
Journal:  PLoS One       Date:  2014-04-14       Impact factor: 3.240

  10 in total

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