Spacer mutations in the lac ps promoter.
- 1 February 1982
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 79 (4) , 1069-1072
- https://doi.org/10.1073/pnas.79.4.1069
Abstract
Mutations have been constructed that delete either 1 or 2 base pairs near position -19 in the [Escherichia coli] lac ps promoter. Deletion of either of 2 adjacent base pairs increases the rate of open complex formation by nearly an order of magnitude. Two promoters that have different single-base deletions are indistinguishable by either their rates of open complex formation or stability of the open complexes once formed. However, simultaneous deletion of both base pairs produces a promoter that forms complexes at a rate similar to that of the unmodified DNA sequence. The maximal rate of open complex formation is achieved at a spacer length of 17 base pairs, the most frequently occurring spacer length among promoters. The spacing between the 2 strongly conserved regions of sequence homology is apparently an important determinant of the rate of open complex formation. A model is suggested that proposes that 3 important promoter elements, the -10 region, the -35 region and the spacer region, act simultaneously to facilitate open complex formation by RNA polymerase.This publication has 13 references indexed in Scilit:
- [57] Sequencing end-labeled DNA with base-specific chemical cleavagesPublished by Elsevier ,2004
- Kinetic investigation of the mechanism of RNA polymerase binding to mutant lac promoters.Journal of Biological Chemistry, 1980
- E. coli RNA polymerase interacts homologously with two different promotersCell, 1980
- Alterations in two conserved regions of promoter sequence lead to altered rates of polymerase binding and levels of gene expressionNucleic Acids Research, 1980
- REGULATORY SEQUENCES INVOLVED IN THE PROMOTION AND TERMINATION OF RNA TRANSCRIPTIONAnnual Review of Genetics, 1979
- A rapid alkaline extraction procedure for screening recombinant plasmid DNANucleic Acids Research, 1979
- Promoter mutations in the transfer RNA gene tyrT of Escherichia coli.Proceedings of the National Academy of Sciences, 1979
- In vitro analysis of the Escherichia coli RNA polymerase interaction with wild-type and mutant lactose promotersJournal of Molecular Biology, 1978
- A simple procedure for resolution of Escherichia coli RNA polymerase holoenzyme from core polymeraseArchives of Biochemistry and Biophysics, 1977
- Purification and Further Properties of Single‐Strand‐Specific Nuclease from Aspergillus oryzaeEuropean Journal of Biochemistry, 1973