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Distinctive topologies of partner-switching signaling networks correlate with their physiological roles.

Distinctive topologies of partner-switching signaling networks correlate with their physiological roles. Research Abstract Details 

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  • Distinctive topologies of partner-switching signaling networks correlate with their physiological roles. Abstract Text:

    oleg a igoshinOleg A Igoshin,margaret s brodyMargaret S Brody,chester w priceChester W Price,michael a savageauMichael A Savageau,

    Regulatory networks controlling bacterial gene expression often evolve from common origins and share homologous proteins and similar network motifs. However, when functioning in different physiological contexts, these motifs may be re-arranged with different topologies that significantly affect network performance. Here we analyze two related signaling networks in the bacterium Bacillus subtilis in order to assess the consequences of their different topologies, with the aim of formulating design principles applicable to other systems. These two networks control the activities of the general stress response factor sigma(B) and the first sporulation-specific factor sigma(F). Both networks have at their core a "partner-switching" mechanism, in which an anti-sigma factor forms alternate complexes either with the sigma factor, holding it inactive, or with an anti-anti-sigma factor, thereby freeing sigma. However, clear differences in network structure are apparent: the anti-sigma factor for sigma(F) forms a long-lived, "dead-end" complex with its anti-anti-sigma factor and ADP, whereas the genes encoding sigma(B) and its network partners lie in a sigma(B)-controlled operon, resulting in positive and negative feedback loops. We constructed mathematical models of both networks and examined which features were critical for the performance of each design. The sigma(F) model predicts that the self-enhancing formation of the dead-end complex transforms the network into a largely irreversible hysteretic switch; the simulations reported here also demonstrate that hysteresis and slow turn off kinetics are the only two system properties associated with this complex formation. By contrast, the sigma(B) model predicts that the positive and negative feedback loops produce graded, reversible behavior with high regulatory capacity and fast response time. Our models demonstrate how alterations in network design result in different system properties that correlate with regulatory demands. These design principles agree with the known or suspected roles of similar networks in diverse bacteria.

    Distinctive topologies of partner-switching signaling networks correlate with their physiological roles. Publishing Authors By Initials

    oa igoshinOA Igoshin,ms brodyMS Brody,cw priceCW Price,ma savageauMA Savageau,

    For similar cells: spores: spores, bacterial research abstracts see: cells: spores: spores, bacterial research

    PUBMED ID PMID:

    MEDLINE DATE:

    Distinctive topologies of partner-switching signaling networks correlate with their physiological roles. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Journal of molecular biology

    VOLUME: 369

    Page Numbers: 1333-52

    Journal Abbreviation: J. Mol. Biol.

    ISSN: 0022-2836

    DAY: 14

    MONTH: 04

    YEAR: 2007

    Distinctive topologies of partner-switching signaling networks correlate with their physiological roles. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 2985088

    Distinctive topologies of partner-switching signaling networks correlate with their physiological roles. Keywords Mesh Terms:

    KEYWORDS: Spores, Bacterial

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Distinctive topologies of partner-switching signaling networks correlate with their physiological roles. Information

    Substance Name: Adenosine Diphosphate

    Registry Number: 58-64-0

    Grant and Affiliation Information for Distinctive topologies of partner-switching signaling networks correlate with their physiological roles.

    AFFILIATION: Department of Biomedical Engineering, University of California, Davis, CA 95616, USA.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NIGMS

    GRANT: R01-GM42077

    ACRONYM: GM

    MEDLINETA: J Mol Biol

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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