A Characterization of Scale Invariant Responses in Enzymatic Networks

An ubiquitous property of biological sensory systems is adaptation: a step increase in stimulus triggers an initial change in a biochemical or physiological response, followed by a more gradual relaxation toward a basal, pre-stimulus level. Adaptation helps maintain essential variables within acceptable bounds and allows organisms to readjust themselves to an optimum and non-saturating sensitivity range when faced with a prolonged change in their environment. Recently, it was shown theoretically and experimentally that many adapting systems, both at the organism and single-cell level, enjoy a remarkable additional feature: scale invariance, meaning that the initial, transient behavior remains (approximately) the same even when the background signal level is scaled. In this work, we set out to investigate under what conditions a broadly used model of biochemical enzymatic networks will exhibit scale-invariant behavior. An exhaustive computational study led us to discover a new property of surprising simplicity and generality, uniform linearizations with fast output (ULFO), whose validity we show is both necessary and sufficient for scale invariance of three-node enzymatic networks (and sufficient for any number of nodes). Based on this study, we go on to develop a mathematical explanation of how ULFO results in scale invariance. Our work provides a surprisingly consistent, simple, and general framework for understanding this phenomenon, and results in concrete experimental predictions.

[1]  Pablo A. Iglesias,et al.  MAPK-mediated bimodal gene expression and adaptive gradient sensing in yeast , 2007, Nature.

[2]  Giuseppe Pugliese,et al.  High glucose level inhibits capacitative Ca2 + influx in cultured rat mesangial cells by a protein kinase C-dependent mechanism , 1997, Diabetologia.

[3]  James P. Keener,et al.  Mathematical physiology , 1998 .

[4]  D. Lauffenburger,et al.  A Computational Study of Feedback Effects on Signal Dynamics in a Mitogen‐Activated Protein Kinase (MAPK) Pathway Model , 2001, Biotechnology progress.

[5]  Lea Goentoro,et al.  Evidence that fold-change, and not absolute level, of beta-catenin dictates Wnt signaling. , 2009, Molecular cell.

[6]  W. Lim,et al.  Defining Network Topologies that Can Achieve Biochemical Adaptation , 2009, Cell.

[7]  Casim A. Sarkar,et al.  Robust Network Topologies for Generating Switch-Like Cellular Responses , 2011, PLoS Comput. Biol..

[8]  Shinya Kuroda,et al.  Prediction and validation of the distinct dynamics of transient and sustained ERK activation , 2005, Nature Cell Biology.

[9]  M. Karin,et al.  Mammalian MAP kinase signalling cascades , 2001, Nature.

[10]  Eduardo D. Sontag,et al.  Symmetry invariance for adapting biological systems , 2010, SIAM J. Appl. Dyn. Syst..

[11]  Erol Cerasi,et al.  Modeling phasic insulin release: immediate and time-dependent effects of glucose. , 2002, Diabetes.

[12]  Yuhai Tu,et al.  Perfect and near-perfect adaptation in a model of bacterial chemotaxis. , 2002, Biophysical journal.

[13]  Eduardo D. Sontag,et al.  Adaptation and regulation with signal detection implies internal model , 2003, Syst. Control. Lett..

[14]  Gideon Bollag,et al.  GTPase activating proteins: critical regulators of intracellular signaling. , 2002, Biochimica et biophysica acta.

[15]  Andreas Kremling,et al.  A feed-forward loop guarantees robust behavior in Escherichia coli carbohydrate uptake , 2008, Bioinform..

[16]  J. Bamburg,et al.  Regulating actin-filament dynamics in vivo. , 2000, Trends in biochemical sciences.

[17]  H. Berg,et al.  Adaptation kinetics in bacterial chemotaxis , 1983, Journal of bacteriology.

[18]  Eduardo Sontag,et al.  Fold-change detection and scalar symmetry of sensory input fields , 2010, Proceedings of the National Academy of Sciences.

[19]  R. L. Iman Appendix A: Latin Hypercube Sampling 1 , 2001 .

[20]  E D Sontag,et al.  Remarks on feedforward circuits, adaptation, and pulse memory. , 2008, IET systems biology.

[21]  C. Widmann,et al.  Mitogen-activated protein kinase: conservation of a three-kinase module from yeast to human. , 1999, Physiological reviews.

[22]  Zhen Xie,et al.  Molecular Systems Biology Peer Review Process File Synthetic Incoherent Feed-forward Circuits Show Adaptation to the Amount of Their Genetic Template. Transaction Report , 2022 .

[23]  Prahlad T. Ram,et al.  Formation of Regulatory Patterns During Signal Propagation in a Mammalian Cellular Network , 2005, Science.

[24]  Paul François,et al.  A case study of evolutionary computation of biochemical adaptation , 2008, Physical biology.

[25]  E. Groisman,et al.  Making informed decisions: regulatory interactions between two-component systems. , 2003, Trends in microbiology.

[26]  Eduardo Sontag,et al.  Untangling the wires: A strategy to trace functional interactions in signaling and gene networks , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[27]  D. Burke,et al.  The spindle assembly and spindle position checkpoints. , 2003, Annual review of genetics.

[28]  U Alon,et al.  The incoherent feed-forward loop accelerates the response-time of the gal system of Escherichia coli. , 2006, Journal of molecular biology.

[29]  G. Karp,et al.  Cell and Molecular Biology , 2002 .

[30]  Uri Alon,et al.  Dynamics and variability of ERK2 response to EGF in individual living cells. , 2009, Molecular cell.

[31]  R. Evans,et al.  ADP is not an agonist at P2X1 receptors: evidence for separate receptors stimulated by ATP and ADP on human platelets , 2000, British journal of pharmacology.

[32]  Y. Tu,et al.  Logarithmic sensing in Escherichia coli bacterial chemotaxis. , 2009, Biophysical journal.

[33]  Eduardo D. Sontag,et al.  Mathematical Control Theory: Deterministic Finite Dimensional Systems , 1990 .

[34]  A. Grossman Genetic networks controlling the initiation of sporulation and the development of genetic competence in Bacillus subtilis. , 1995, Annual review of genetics.

[35]  M. Sulis,et al.  PTEN: from pathology to biology. , 2003, Trends in cell biology.

[36]  F. Young Biochemistry , 1955, The Indian Medical Gazette.

[37]  J. Adler,et al.  The Range of Attractant Concentrations for Bacterial Chemotaxis and the Threshold and Size of Response over This Range , 1973, The Journal of general physiology.

[38]  Pablo A. Iglesias,et al.  An approximate internal model principle: Applications to nonlinear models of biological systems , 2008 .

[39]  Alex Groisman,et al.  Incoherent Feedforward Control Governs Adaptation of Activated Ras in a Eukaryotic Chemotaxis Pathway , 2012, Science Signaling.

[40]  Chi-Ying F. Huang,et al.  Ultrasensitivity in the mitogen-activated protein kinase cascade. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[41]  Michael P Vitek,et al.  Nitric oxide regulates matrix metalloproteinase-9 activity by guanylyl-cyclase-dependent and -independent pathways , 2007, Proceedings of the National Academy of Sciences.

[42]  A. Muscella,et al.  Increase of [Ca(2+)](i) via activation of ATP receptors in PC-Cl3 rat thyroid cell line. , 2002, Cellular signalling.

[43]  Pablo A. Iglesias,et al.  Feedback Control in Intracellular Signaling Pathways: Regulating Chemotaxis in Dictyostelium Discoideum , 2003, Eur. J. Control.

[44]  Takashi Nakakuki,et al.  Quantitative transcriptional control of ErbB receptor signaling undergoes graded to biphasic response for cell differentiation. , 2006, The Journal of Biological Chemistry.

[45]  Arthur L. Benton,et al.  Foundations of Physiological Psychology , 1968 .

[46]  H. Berg,et al.  A modular gradient-sensing network for chemotaxis in Escherichia coli revealed by responses to time-varying stimuli , 2010, Molecular systems biology.

[47]  Roman Stocker,et al.  Response rescaling in bacterial chemotaxis , 2011, Proceedings of the National Academy of Sciences.

[48]  A. van Oudenaarden,et al.  MicroRNA-mediated feedback and feedforward loops are recurrent network motifs in mammals. , 2007, Molecular cell.

[49]  J. Doyle,et al.  Robust perfect adaptation in bacterial chemotaxis through integral feedback control. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[50]  M. West,et al.  Origin of bistability underlying mammalian cell cycle entry , 2011, Molecular systems biology.