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Contribution of Physical Interactions to Signaling Specificity between a Diguanylate Cyclase and Its Effector

Cyclic diguanylate (c-di-GMP) is a bacterial second messenger that controls multiple cellular processes. c-di-GMP networks have up to dozens of diguanylate cyclases (DGCs) that synthesize c-di-GMP along with many c-di-GMP-responsive target proteins that can bind and respond to this signal. For such...

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Autores principales: Dahlstrom, Kurt M., Giglio, Krista M., Collins, Alan J., Sondermann, Holger, O’Toole, George A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676286/
https://www.ncbi.nlm.nih.gov/pubmed/26670387
http://dx.doi.org/10.1128/mBio.01978-15
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author Dahlstrom, Kurt M.
Giglio, Krista M.
Collins, Alan J.
Sondermann, Holger
O’Toole, George A.
author_facet Dahlstrom, Kurt M.
Giglio, Krista M.
Collins, Alan J.
Sondermann, Holger
O’Toole, George A.
author_sort Dahlstrom, Kurt M.
collection PubMed
description Cyclic diguanylate (c-di-GMP) is a bacterial second messenger that controls multiple cellular processes. c-di-GMP networks have up to dozens of diguanylate cyclases (DGCs) that synthesize c-di-GMP along with many c-di-GMP-responsive target proteins that can bind and respond to this signal. For such networks to have order, a mechanism(s) likely exists that allow DGCs to specifically signal their targets, and it has been suggested that physical interactions might provide such specificity. Our results show a DGC from Pseudomonas fluorescens physically interacting with its target protein at a conserved interface, and this interface can be predictive of DGC-target protein interactions. Furthermore, we demonstrate that physical interaction is necessary for the DGC to maximally signal its target. If such “local signaling” is a theme for even a fraction of the DGCs used by bacteria, it becomes possible to posit a model whereby physical interaction allows a DGC to directly signal its target protein, which in turn may help curtail undesired cross talk with other members of the network.
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spelling pubmed-46762862015-12-16 Contribution of Physical Interactions to Signaling Specificity between a Diguanylate Cyclase and Its Effector Dahlstrom, Kurt M. Giglio, Krista M. Collins, Alan J. Sondermann, Holger O’Toole, George A. mBio Research Article Cyclic diguanylate (c-di-GMP) is a bacterial second messenger that controls multiple cellular processes. c-di-GMP networks have up to dozens of diguanylate cyclases (DGCs) that synthesize c-di-GMP along with many c-di-GMP-responsive target proteins that can bind and respond to this signal. For such networks to have order, a mechanism(s) likely exists that allow DGCs to specifically signal their targets, and it has been suggested that physical interactions might provide such specificity. Our results show a DGC from Pseudomonas fluorescens physically interacting with its target protein at a conserved interface, and this interface can be predictive of DGC-target protein interactions. Furthermore, we demonstrate that physical interaction is necessary for the DGC to maximally signal its target. If such “local signaling” is a theme for even a fraction of the DGCs used by bacteria, it becomes possible to posit a model whereby physical interaction allows a DGC to directly signal its target protein, which in turn may help curtail undesired cross talk with other members of the network. American Society of Microbiology 2015-12-15 /pmc/articles/PMC4676286/ /pubmed/26670387 http://dx.doi.org/10.1128/mBio.01978-15 Text en Copyright © 2015 Dahlstrom et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dahlstrom, Kurt M.
Giglio, Krista M.
Collins, Alan J.
Sondermann, Holger
O’Toole, George A.
Contribution of Physical Interactions to Signaling Specificity between a Diguanylate Cyclase and Its Effector
title Contribution of Physical Interactions to Signaling Specificity between a Diguanylate Cyclase and Its Effector
title_full Contribution of Physical Interactions to Signaling Specificity between a Diguanylate Cyclase and Its Effector
title_fullStr Contribution of Physical Interactions to Signaling Specificity between a Diguanylate Cyclase and Its Effector
title_full_unstemmed Contribution of Physical Interactions to Signaling Specificity between a Diguanylate Cyclase and Its Effector
title_short Contribution of Physical Interactions to Signaling Specificity between a Diguanylate Cyclase and Its Effector
title_sort contribution of physical interactions to signaling specificity between a diguanylate cyclase and its effector
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676286/
https://www.ncbi.nlm.nih.gov/pubmed/26670387
http://dx.doi.org/10.1128/mBio.01978-15
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