Genetic analysis of pertussis toxin promoter activation in Bordetella pertussis.

Abstract:

:Bordetella pertussis regulates expression of its virulence factors such as pertussis toxin (Ptx) via the bvg locus, which encodes a two-component system composed of a sensor protein, BvgS, and a transcription activator, BvgA. We used a ptx-lac fusion on the B. pertussis chromosome to analyse promoter activation by alteration of specific sequences upstream of and within the promoter. Our data demonstrate that a pair of heptanucleotide inverted repeats separated by a turn of the DNA helix within the upstream repeat region (centred around nucleotide -136.5) are crucial cis-activating elements, and probably represent the initial BvgA-binding site. In addition, we demonstrate that the sequence between these repeats and the promoter plays a role in activation. Our data are most consistent with a model of co-operative binding of BvgA dimers to this intervening region and interaction with RNA polymerase at the promoter to activate ptx transcription. In the core promoter region both the non-consensus 21 bp spacing and the specific sequence between the -35 and -10 elements are crucial for promoter activity.

journal_name

Mol Microbiol

journal_title

Molecular microbiology

authors

Marques RR,Carbonetti NH

doi

10.1046/j.1365-2958.1997.4371792.x

subject

Has Abstract

pub_date

1997-06-01 00:00:00

pages

1215-24

issue

6

eissn

0950-382X

issn

1365-2958

journal_volume

24

pub_type

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