Excess information at bacteriophage T7 genomic promoters detected by a random cloning technique
- 1 January 1989
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 17 (2) , 659-674
- https://doi.org/10.1093/nar/17.2.659
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 gnomic promoters have significantly more information than the polymerase needs. The excess may represent the binding site of another protein.This publication has 31 references indexed in Scilit:
- [35] The use of random-sequence oligonucleotides for determining consensus sequencesPublished by Elsevier ,1987
- A bacteriophage T7 RNA polymerase/promoter system for controlled exclusive expression of specific genes.Proceedings of the National Academy of Sciences, 1985
- Cloning and expression of the gene for bacteriophage T7 RNA polymerase.Proceedings of the National Academy of Sciences, 1984
- Complete nucleotide sequence of bacteriophage T7 DNA and the locations of T7 genetic elementsJournal of Molecular Biology, 1983
- Identification of a potential control region in bacteriophage T7 late promotersNature, 1982
- Utilization of bacteriophage T7 late promoters in recombinant plasmids during infectionJournal of Molecular Biology, 1981
- A set of synthetic oligodeoxyribonucleotide primers for DNA sequencing in the plasmid vector pBR322Gene, 1981
- T7 Ribonucleic acid polymerase-promoter interactionsBiochemistry, 1981
- Analysis of gene control signals by DNA fusion and cloning in Escherichia coliJournal of Molecular Biology, 1980
- Plasmid pKC7: A vector containing ten restriction endonuclease sites suitable for cloning DNA segmentsGene, 1979