TY - JOUR
T1 - Excess information at bacteriophage T7 genomic promoters detected by a random cloning technique
AU - Schneider, Thomas D.
AU - Stormo, Gary D.
N1 - Funding Information:
ACKNOWLEDGEMENTS We thank W. Studier for BL21/DE3 and 4107(26), M. Casadaban for MC1061, B. Weiss for pKC7, J. Binkley for a careful DNA synthesis, A. Pelletier for suggesting the use of carbenicillin, C. Tuerk and D. McPheeters for help with DNA and RNA sequencing, C. E. Lawrence and G. W. Alvord for statistical advice, P. Lemkin for help with gel scanning, L. Sinclair, M. Nawroz and T. Hollingsworth for technical help, and A. Barber, D. Court, A. Konopka, D. Lipman, J. Maizel, E. Max, H. Nash, P. Rogan, J. Ruckman, K. Rudd, J. Strathern, J. Spouge, and R. Weisberg for critically reading the manuscript. We give special thanks to L. Gold who supported and guided this project from its inception. This work was supported in part by NIH grant GM28755.
PY - 1989/1/25
Y1 - 1989/1/25
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=0024533114&partnerID=8YFLogxK
U2 - 10.1093/nar/17.2.659
DO - 10.1093/nar/17.2.659
M3 - Article
C2 - 2915926
AN - SCOPUS:0024533114
SN - 0305-1048
VL - 17
SP - 659
EP - 674
JO - Nucleic acids research
JF - Nucleic acids research
IS - 2
ER -