Abstract
At some bacterial promoters, a 5'-TG-3' sequence element, located one base upstream of the -10 hexamer element, provides an essential motif necessary for transcription initiation. We have identified a mutant of the Escherichia coli RNA polymerase sigma70 subunit that has an altered preference for base sequences in this 'extended -10' region. We show that this mutant sigma70 subunit substantially increases transcription from promoters bearing 5'-TC-3' or 5'-TT-3' instead of a 5'-TG-3' motif, located one base upstream of the -10 hexamer. The mutant results from a single base pair substitution in the rpoD gene that causes a Glu to Gly change at position 458 of sigma70. This substitution identifies a functional region in sigma70 that is immediately adjacent to the well-characterized region 2.4 (positions 434-453, previously shown to contact the -10 hexamer). From these results, we conclude that this region (which we name region 2.5) is involved in contacting the 5'-TG-3' motif found at some bacterial promoters: thus, extended -10 regions are recognized by an extended region 2 of the RNA polymerase sigma70 subunit.
MeSH Terms
Amino Acid Sequence
Base Sequence
Binding Sites
Conserved Sequence
DNA, Bacterial/metabolism
DNA-Directed RNA Polymerases/genetics,metabolism
Escherichia coli/enzymology,genetics
Molecular Sequence Data
Mutagenesis, Site-Directed
Promoter Regions, Genetic
Recombinant Fusion Proteins/genetics,metabolism
Sigma Factor/genetics,metabolism
Chemicals
DNA, Bacterial
Recombinant Fusion Proteins
Sigma Factor
RNA polymerase sigma 70
DNA-Directed RNA Polymerases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Barne K A
School of Biochemistry, The University of Birmingham, Edgbaston, UK.
Bown J A
Busby S J
Minchin S D
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