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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Microbiology
2015
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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. |
format | Online Article Text |
id | pubmed-4676286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Society of Microbiology |
record_format | MEDLINE/PubMed |
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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