Home LiteratureArticle Details
PMID: 2915926 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

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

Nucleic acids research ·Vol. 17 ·No. 2 ·1989-01-25 ·Pages 659-74

Schneider TD, Stormo GD

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.

MeSH Terms
Base Composition Base Sequence Cloning, Molecular/methods DNA, Viral/chemical synthesis,isolation & purification Genes, Viral Mathematical Computing Models, Genetic Molecular Sequence Data Promoter Regions, Genetic T-Phages/genetics
Chemicals
DNA, Viral
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Schneider T D
National Cancer Institute, Laboratory of Mathematical Biology, Frederick, MD 21701.
Stormo G D
References (29)
29 references, click to expand
  1. Plasmid pKC7: a vector containing ten restriction endonuclease sites suitable for cloning DNA segments.
    Gene. 1979 Sep;7(1):79-82 PMID: 159209
  2. The use of random-sequence oligonucleotides for determining consensus sequences.
    Methods Enzymol. 1987;155:568-82 PMID: 2828877
  3. Analysis of gene control signals by DNA fusion and cloning in Escherichia coli.
    J Mol Biol. 1980 Apr;138(2):179-207 PMID: 6997493
  4. T7 ribonucleic acid polymerase-promotor interactions.
    Biochemistry. 1981 Aug 18;20(17):4884-92 PMID: 6271174
  5. Utilization of bacteriophage T7 late promoters in recombinant plasmids during infection.
    J Mol Biol. 1981 Dec 15;153(3):527-44 PMID: 7040687
  6. A set of synthetic oligodeoxyribonucleotide primers for DNA sequencing in the plasmid vector pBR322.
    Gene. 1981 Dec;16(1-3):21-6 PMID: 6282692
  7. Identification of a potential control region in bacteriophage T7 late promoters.
    Nature. 1982 Oct 14;299(5884):653-6 PMID: 7121598
  8. Complete nucleotide sequence of bacteriophage T7 DNA and the locations of T7 genetic elements.
    J Mol Biol. 1983 Jun 5;166(4):477-535 PMID: 6864790
  9. Mutagenesis of the three bases preceding the start codon of the beta-galactosidase mRNA and its effect on translation in Escherichia coli.
    EMBO J. 1984 Mar;3(3):623-9 PMID: 6425057
  10. Cloning and expression of the gene for bacteriophage T7 RNA polymerase.
    Proc Natl Acad Sci U S A. 1984 Apr;81(7):2035-9 PMID: 6371808
  11. A bacteriophage T7 RNA polymerase/promoter system for controlled exclusive expression of specific genes.
    Proc Natl Acad Sci U S A. 1985 Feb;82(4):1074-8 PMID: 3156376
  12. Bacteriophage T7 late promoters with point mutations: quantitative footprinting and in vivo expression.
    Nucleic Acids Res. 1988 May 25;16(10):4511-24 PMID: 3288970
  13. Computer methods for analyzing sequence recognition of nucleic acids.
    Annu Rev Biophys Biophys Chem. 1988;17:241-63 PMID: 3293587
  14. A critical test of a current theory of genetic recombination in bacteriophage.
    Genetics. 1962 Feb;47:187-208 PMID: 13916671
  15. New RNA polymerase from Escherichia coli infected with bacteriophage T7.
    Nature. 1970 Oct 17;228(5268):227-31 PMID: 4920917
  16. DNA sequencing with chain-terminating inhibitors.
    Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463-7 PMID: 271968
  17. T7 RNA polymerase: promoter structure and polymerase binding.
    Biochemistry. 1979 Feb 6;18(3):528-37 PMID: 369603
  18. Four T7 RNA polymerase promoters contain an identical 23 bp sequence.
    Cell. 1979 Apr;16(4):815-25 PMID: 455451
  19. Prolonged incubation in calcium chloride improves the competence of Escherichia coli cells.
    Gene. 1979 May;6(1):23-8 PMID: 383576
  20. Supercoil sequencing: a fast and simple method for sequencing plasmid DNA.
    DNA. 1985 Apr;4(2):165-70 PMID: 3996185
  21. Sequence landscapes.
    Nucleic Acids Res. 1986 Jan 10;14(1):141-58 PMID: 3753762
  22. Information content of binding sites on nucleotide sequences.
    J Mol Biol. 1986 Apr 5;188(3):415-31 PMID: 3525846
  23. Quantitative analysis of the relationship between nucleotide sequence and functional activity.
    Nucleic Acids Res. 1986 Aug 26;14(16):6661-79 PMID: 3092188
  24. Promoters selected from random DNA sequences.
    Proc Natl Acad Sci U S A. 1986 Oct;83(19):7405-9 PMID: 3532112
  25. Use of bacteriophage T7 RNA polymerase to direct selective high-level expression of cloned genes.
    J Mol Biol. 1986 May 5;189(1):113-30 PMID: 3537305
  26. Construction of bacteriophage T7 late promoters with point mutations and characterization by in vitro transcription properties.
    Nucleic Acids Res. 1987 Jul 10;15(13):5413-32 PMID: 3299271
  27. Oligoribonucleotide synthesis using T7 RNA polymerase and synthetic DNA templates.
    Nucleic Acids Res. 1987 Nov 11;15(21):8783-98 PMID: 3684574
  28. Mutagenesis with degenerate oligonucleotides: an efficient method for saturating a defined DNA region with base pair substitutions.
    Methods Enzymol. 1987;155:558-68 PMID: 3481016
  29. A rapid alkaline extraction procedure for screening recombinant plasmid DNA.
    Nucleic Acids Res. 1979 Nov 24;7(6):1513-23 PMID: 388356
Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1989-01-25
Pages
659-74
Language
English
Region
England
NLM ID
0411011
PMCID
PMC331610
Subset
IM
Grants
NIGMS NIH HHS · GM28755 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]