The activity of the Pseudomonas aeruginosa virulence regulator sVreI is modulated by the anti-s factor VreR and the transcription factor PhoB

Gene regulation in bacteria is primarily controlled at the level of transcription initiation by modifying the affinity of the RNA polymerase (RNAP) for the promoter. This control often occurs through the substitution of the RNAP sigma () subunit. Next to the primary  factor, most bacteria contain...

Full description

Bibliographic Details
Main Authors: Jose M Quesada, Joaquin R Otero-Asman, Karlijn C Bastiaansen, Cristina Civantos, María A Llamas
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-08-01
Series:Frontiers in Microbiology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01159/full
_version_ 1818267318475554816
author Jose M Quesada
Joaquin R Otero-Asman
Karlijn C Bastiaansen
Karlijn C Bastiaansen
Cristina Civantos
María A Llamas
author_facet Jose M Quesada
Joaquin R Otero-Asman
Karlijn C Bastiaansen
Karlijn C Bastiaansen
Cristina Civantos
María A Llamas
author_sort Jose M Quesada
collection DOAJ
description Gene regulation in bacteria is primarily controlled at the level of transcription initiation by modifying the affinity of the RNA polymerase (RNAP) for the promoter. This control often occurs through the substitution of the RNAP sigma () subunit. Next to the primary  factor, most bacteria contain a variable number of alternative  factors of which the extracytoplasmic function group (ECF) is predominant. Pseudomonas aeruginosa contains nineteen ECF, including the virulence regulator VreI. VreI is encoded by the vreAIR operon, which also encodes a receptor-like protein (VreA) and an anti- factor (VreR). These three proteins form a signal transduction pathway known as PUMA3, which controls expression of P. aeruginosa virulence functions. Expression of the vreAIR operon occurs under inorganic phosphate (Pi) limitation and requires the PhoB transcription factor. Intriguingly, the genes of the VreI regulon are also expressed in low Pi despite the fact that the VreI repressor, the anti- factor VreR, is also produced in this condition. Here we show that although VreI is partially active under Pi starvation, maximal transcription of the VreI regulon genes requires the removal of VreR. This strongly suggests that an extra signal, probably host-derived, is required in vivo for full VreI activation. Furthermore, we demonstrate that the activity of VreI is modulated not only by VreR but also by the transcription factor PhoB. Presence of this regulator is an absolute requirement for VreI to complex the DNA and initiate transcription of the PUMA3 regulon. The potential DNA binding sites of these two proteins, which include a pho box and –10 and –35 elements, are proposed.
first_indexed 2024-12-12T20:20:41Z
format Article
id doaj.art-82ee7e8f9eae4632b481f9e80422e13e
institution Directory Open Access Journal
issn 1664-302X
language English
last_indexed 2024-12-12T20:20:41Z
publishDate 2016-08-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Microbiology
spelling doaj.art-82ee7e8f9eae4632b481f9e80422e13e2022-12-22T00:13:16ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2016-08-01710.3389/fmicb.2016.01159208512The activity of the Pseudomonas aeruginosa virulence regulator sVreI is modulated by the anti-s factor VreR and the transcription factor PhoBJose M Quesada0Joaquin R Otero-Asman1Karlijn C Bastiaansen2Karlijn C Bastiaansen3Cristina Civantos4María A Llamas5Estación Experimental del Zaidín-Consejo Superior de investifgaciones Científicas (CSIC)Estación Experimental del Zaidín-Consejo Superior de investifgaciones Científicas (CSIC)Estación Experimental del Zaidín-Consejo Superior de investifgaciones Científicas (CSIC)VU University AmsterdamEstación Experimental del Zaidín-Consejo Superior de investifgaciones Científicas (CSIC)Estación Experimental del Zaidín-Consejo Superior de investifgaciones Científicas (CSIC)Gene regulation in bacteria is primarily controlled at the level of transcription initiation by modifying the affinity of the RNA polymerase (RNAP) for the promoter. This control often occurs through the substitution of the RNAP sigma () subunit. Next to the primary  factor, most bacteria contain a variable number of alternative  factors of which the extracytoplasmic function group (ECF) is predominant. Pseudomonas aeruginosa contains nineteen ECF, including the virulence regulator VreI. VreI is encoded by the vreAIR operon, which also encodes a receptor-like protein (VreA) and an anti- factor (VreR). These three proteins form a signal transduction pathway known as PUMA3, which controls expression of P. aeruginosa virulence functions. Expression of the vreAIR operon occurs under inorganic phosphate (Pi) limitation and requires the PhoB transcription factor. Intriguingly, the genes of the VreI regulon are also expressed in low Pi despite the fact that the VreI repressor, the anti- factor VreR, is also produced in this condition. Here we show that although VreI is partially active under Pi starvation, maximal transcription of the VreI regulon genes requires the removal of VreR. This strongly suggests that an extra signal, probably host-derived, is required in vivo for full VreI activation. Furthermore, we demonstrate that the activity of VreI is modulated not only by VreR but also by the transcription factor PhoB. Presence of this regulator is an absolute requirement for VreI to complex the DNA and initiate transcription of the PUMA3 regulon. The potential DNA binding sites of these two proteins, which include a pho box and –10 and –35 elements, are proposed.http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01159/fullPseudomonas aeruginosaSignal Transductiongene regulationPhosphate starvationExtracytoplasmic function sigma factorPhob
spellingShingle Jose M Quesada
Joaquin R Otero-Asman
Karlijn C Bastiaansen
Karlijn C Bastiaansen
Cristina Civantos
María A Llamas
The activity of the Pseudomonas aeruginosa virulence regulator sVreI is modulated by the anti-s factor VreR and the transcription factor PhoB
Frontiers in Microbiology
Pseudomonas aeruginosa
Signal Transduction
gene regulation
Phosphate starvation
Extracytoplasmic function sigma factor
Phob
title The activity of the Pseudomonas aeruginosa virulence regulator sVreI is modulated by the anti-s factor VreR and the transcription factor PhoB
title_full The activity of the Pseudomonas aeruginosa virulence regulator sVreI is modulated by the anti-s factor VreR and the transcription factor PhoB
title_fullStr The activity of the Pseudomonas aeruginosa virulence regulator sVreI is modulated by the anti-s factor VreR and the transcription factor PhoB
title_full_unstemmed The activity of the Pseudomonas aeruginosa virulence regulator sVreI is modulated by the anti-s factor VreR and the transcription factor PhoB
title_short The activity of the Pseudomonas aeruginosa virulence regulator sVreI is modulated by the anti-s factor VreR and the transcription factor PhoB
title_sort activity of the pseudomonas aeruginosa virulence regulator svrei is modulated by the anti s factor vrer and the transcription factor phob
topic Pseudomonas aeruginosa
Signal Transduction
gene regulation
Phosphate starvation
Extracytoplasmic function sigma factor
Phob
url http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01159/full
work_keys_str_mv AT josemquesada theactivityofthepseudomonasaeruginosavirulenceregulatorsvreiismodulatedbytheantisfactorvrerandthetranscriptionfactorphob
AT joaquinroteroasman theactivityofthepseudomonasaeruginosavirulenceregulatorsvreiismodulatedbytheantisfactorvrerandthetranscriptionfactorphob
AT karlijncbastiaansen theactivityofthepseudomonasaeruginosavirulenceregulatorsvreiismodulatedbytheantisfactorvrerandthetranscriptionfactorphob
AT karlijncbastiaansen theactivityofthepseudomonasaeruginosavirulenceregulatorsvreiismodulatedbytheantisfactorvrerandthetranscriptionfactorphob
AT cristinacivantos theactivityofthepseudomonasaeruginosavirulenceregulatorsvreiismodulatedbytheantisfactorvrerandthetranscriptionfactorphob
AT mariaallamas theactivityofthepseudomonasaeruginosavirulenceregulatorsvreiismodulatedbytheantisfactorvrerandthetranscriptionfactorphob
AT josemquesada activityofthepseudomonasaeruginosavirulenceregulatorsvreiismodulatedbytheantisfactorvrerandthetranscriptionfactorphob
AT joaquinroteroasman activityofthepseudomonasaeruginosavirulenceregulatorsvreiismodulatedbytheantisfactorvrerandthetranscriptionfactorphob
AT karlijncbastiaansen activityofthepseudomonasaeruginosavirulenceregulatorsvreiismodulatedbytheantisfactorvrerandthetranscriptionfactorphob
AT karlijncbastiaansen activityofthepseudomonasaeruginosavirulenceregulatorsvreiismodulatedbytheantisfactorvrerandthetranscriptionfactorphob
AT cristinacivantos activityofthepseudomonasaeruginosavirulenceregulatorsvreiismodulatedbytheantisfactorvrerandthetranscriptionfactorphob
AT mariaallamas activityofthepseudomonasaeruginosavirulenceregulatorsvreiismodulatedbytheantisfactorvrerandthetranscriptionfactorphob