Literature DB >> 2915926

Excess information at bacteriophage T7 genomic promoters detected by a random cloning technique.

T D Schneider1, G D Stormo.   

Abstract

In our previous analysis of the information at binding sites on nucleic acids, we found that most of the sites examined contain the amount of information expected from their frequency in the genome. The sequences at bacteriophage T7 promoters are an exception, because they are far more conserved (35 bits of information content) than should be necessary to distinguish them from the background of the Escherichia coli genome (17 bits). To determine the information actually used by the T7 RNA polymerase, promoters were chemically synthesized with many variations and those that function well in an in vivo assay were sequenced. Our analysis shows that the polymerase uses 18 bits of information, so the sequences at phage genomic promoters have significantly more information than the polymerase needs. The excess may represent the binding site of another protein.

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Year:  1989        PMID: 2915926      PMCID: PMC331610          DOI: 10.1093/nar/17.2.659

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  29 in total

1.  Plasmid pKC7: a vector containing ten restriction endonuclease sites suitable for cloning DNA segments.

Authors:  R N Rao; S G Rogers
Journal:  Gene       Date:  1979-09       Impact factor: 3.688

2.  The use of random-sequence oligonucleotides for determining consensus sequences.

Authors:  A R Oliphant; K Struhl
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

3.  T7 ribonucleic acid polymerase-promotor interactions.

Authors:  H L Osterman; J E Coleman
Journal:  Biochemistry       Date:  1981-08-18       Impact factor: 3.162

4.  Cloning and expression of the gene for bacteriophage T7 RNA polymerase.

Authors:  P Davanloo; A H Rosenberg; J J Dunn; F W Studier
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

5.  Complete nucleotide sequence of bacteriophage T7 DNA and the locations of T7 genetic elements.

Authors:  J J Dunn; F W Studier
Journal:  J Mol Biol       Date:  1983-06-05       Impact factor: 5.469

6.  Utilization of bacteriophage T7 late promoters in recombinant plasmids during infection.

Authors:  W T McAllister; C Morris; A H Rosenberg; F W Studier
Journal:  J Mol Biol       Date:  1981-12-15       Impact factor: 5.469

7.  Analysis of gene control signals by DNA fusion and cloning in Escherichia coli.

Authors:  M J Casadaban; S N Cohen
Journal:  J Mol Biol       Date:  1980-04       Impact factor: 5.469

8.  Identification of a potential control region in bacteriophage T7 late promoters.

Authors:  L K Jolliffe; A D Carter; W T McAllister
Journal:  Nature       Date:  1982-10-14       Impact factor: 49.962

9.  A set of synthetic oligodeoxyribonucleotide primers for DNA sequencing in the plasmid vector pBR322.

Authors:  R B Wallace; M J Johnson; S V Suggs; K Miyoshi; R Bhatt; K Itakura
Journal:  Gene       Date:  1981-12       Impact factor: 3.688

10.  Mutagenesis of the three bases preceding the start codon of the beta-galactosidase mRNA and its effect on translation in Escherichia coli.

Authors:  A Hui; J Hayflick; K Dinkelspiel; H A de Boer
Journal:  EMBO J       Date:  1984-03       Impact factor: 11.598

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  22 in total

1.  Effects of saturation mutagenesis of the phage SP6 promoter on transcription activity, presented by activity logos.

Authors:  I Shin; J Kim; C R Cantor; C Kang
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-11       Impact factor: 11.205

2.  Evolution of biological information.

Authors:  T D Schneider
Journal:  Nucleic Acids Res       Date:  2000-07-15       Impact factor: 16.971

3.  Strong minor groove base conservation in sequence logos implies DNA distortion or base flipping during replication and transcription initiation.

Authors:  T D Schneider
Journal:  Nucleic Acids Res       Date:  2001-12-01       Impact factor: 16.971

4.  Using deep sequencing to characterize the biophysical mechanism of a transcriptional regulatory sequence.

Authors:  Justin B Kinney; Anand Murugan; Curtis G Callan; Edward C Cox
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-03       Impact factor: 11.205

5.  Specificity of the Mnt protein determined by binding to randomized operators.

Authors:  G D Stormo; M Yoshioka
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-01       Impact factor: 11.205

6.  Critical sequences in the core of the P1 plasmid replication origin.

Authors:  T Brendler; A Abeles; S Austin
Journal:  J Bacteriol       Date:  1991-07       Impact factor: 3.490

7.  T7 promoter contacts essential for promoter activity in vivo.

Authors:  R A Ikeda; C M Ligman; S Warshamana
Journal:  Nucleic Acids Res       Date:  1992-05-25       Impact factor: 16.971

8.  High information conservation implies that at least three proteins bind independently to F plasmid incD repeats.

Authors:  N D Herman; T D Schneider
Journal:  J Bacteriol       Date:  1992-06       Impact factor: 3.490

9.  Cyclic amplification and selection of targets (CASTing) for the myogenin consensus binding site.

Authors:  W E Wright; M Binder; W Funk
Journal:  Mol Cell Biol       Date:  1991-08       Impact factor: 4.272

10.  Binding of the bacteriophage T4 regA protein to mRNA targets: an initiator AUG is required.

Authors:  S Unnithan; L Green; L Morrissey; J Binkley; B Singer; J Karam; L Gold
Journal:  Nucleic Acids Res       Date:  1990-12-11       Impact factor: 16.971

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