Design principles of nuclear receptor signaling: How complex networking improves signal transduction

  • Alexey N. Kolodkin
  • , Frank J. Bruggeman
  • , Nick Plant
  • , Martijn J. Mone
  • , Barbara M. Bakker
  • , Moray J. Campbell
  • , Johannes P. T. M. van Leeuwen
  • , Carsten Carlberg
  • , Jacky L. Snoep
  • , Hans V. Westerhoff*
  • *Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    31 Citations (Scopus)
    122 Downloads (Pure)

    Abstract

    The topology of nuclear receptor (NR) signaling is captured in a systems biological graphical notation. This enables us to identify a number of 'design' aspects of the topology of these networks that might appear unnecessarily complex or even functionally paradoxical. In realistic kinetic models of increasing complexity, calculations show how these features correspond to potentially important design principles, e.g.: (i) cytosolic 'nuclear' receptor may shuttle signal molecules to the nucleus, (ii) the active export of NRs may ensure that there is sufficient receptor protein to capture ligand at the cytoplasmic membrane, (iii) a three conveyor belts design dissipating GTP-free energy, greatly aids response, (iv) the active export of importins may prevent sequestration of NRs by importins in the nucleus and (v) the unspecific nature of the nuclear pore may ensure signal-flux robustness. In addition, the models developed are suitable for implementation in specific cases of NR-mediated signaling, to predict individual receptor functions and differential sensitivity toward physiological and pharmacological ligands. Molecular Systems Biology 6: 446; published online 21 December 2010; doi:10.1038/msb.2010.102

    Original languageEnglish
    Article number446
    Number of pages14
    JournalMolecular Systems Biology
    Volume6
    Issue number1
    DOIs
    Publication statusPublished - Dec-2010

    Keywords

    • biochemical network
    • kinetic model
    • nuclear receptor
    • signaling
    • systems biology
    • LIGAND-BINDING DOMAIN
    • GENERALIZED GLUCOCORTICOID RESISTANCE
    • STEROID-RECEPTORS
    • RESPONSE ELEMENT
    • THYROID-HORMONE
    • IMPORTIN-ALPHA
    • POINT MUTATION
    • LIVING CELLS
    • PROTEIN
    • TRANSLOCATION

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