Defining the consensus sequences ofE.colipromoter elements by random selectio
- 11 August 1988
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 16 (15) , 7673-7684
- https://doi.org/10.1093/nar/16.15.7673
Abstract
The consensus sequence of E.coli promoter elements was determined by the method of random selection. A large collection of hybrid molecules was produced in which random-sequence oligonucleotides were cloned in place of a wild-type promoter element, and functional −10 and −35 E.coli promoter elements were obtained by a genetic selection involving the expression of a structural gene. The DNA sequences and relative levels of function for −10 and −35 elements were determined. The consensus sequences determined by this approach are very similar to those determined by comparing DNA sequences of naturally occuring E.coli promoters. However, no strong correlation is observed between similarity to the consensus and relative level of function. The results are considered in terms of E.coli promoter function and of the general applicability of the random selection methodThis publication has 5 references indexed in Scilit:
- A new class of yeast transcriptional activatorsCell, 1987
- Promoter recognition and promoter strength in the Escherichia coli system.The EMBO Journal, 1987
- Many Random Sequences Functionally Replace the Secretion Signal Sequence of Yeast InvertaseScience, 1987
- Promoters of Escherichia coli: a hierarchy of in vivo strength indicates alternate structures.The EMBO Journal, 1986
- Functional genetic expression of eukaryotic DNA in Escherichia coli.Proceedings of the National Academy of Sciences, 1976