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Infinitesimal homeostasis in three-node input–output networks

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Homeostasis occurs in a system where an output variable is approximately constant on an interval on variation of an input variable \({{\mathcal {I}}}\). Homeostasis plays an important role in the regulation of biological systems, cf.  Ferrell (Cell Syst 2:62–67, 2016), Tang and McMillen (J Theor Biol 408:274–289, 2016), Nijhout et al. (BMC Biol 13:79, 2015), and Nijhout et al. (Wiley Interdiscip Rev Syst Biol Med 11:e1440, 2018). A method for finding homeostasis in mathematical models is given in the control theory literature as points where the derivative of the output variable with respect to \({{\mathcal {I}}}\) is identically zero. Such points are called perfect homeostasis or perfect adaptation. Alternatively, Golubitsky and Stewart (J Math Biol 74:387–407, 2017) use an infinitesimal notion of homeostasis (namely, the derivative of the input–output function is zero at an isolated point) to introduce singularity theory into the study of homeostasis. Reed et al. (Bull Math Biol 79(9):1–24, 2017) give two examples of infinitesimal homeostasis in three-node chemical reaction systems: feedforward excitation and substrate inhibition. In this paper we show that there are 13 different three-node networks leading to 78 three-node input–output network configurations, under the assumption that there is one input node, one output node, and they are distinct. The different configurations are based on which node is the input node and which node is the output node. We show nonetheless that there are only three basic mechanisms for three-node input–output networks that lead to infinitesimal homeostasis and we call them structural homeostasis, Haldane homeostasis, and null-degradation homeostasis. Substantial parts of this classification are given in Ma et al. (Cell 138:760–773, 2009) and Ferrell (2016) among others. Our contributions include giving a complete classification using general admissible systems (Golubitsky and Stewart in Bull Am Math Soc 43:305–364, 2006) rather than specific biochemical models, relating the types of infinitesimal homeostasis to the graph theoretic existence of simple paths, and providing the basis to use singularity theory to study higher codimension homeostasis singularities such as the chair singularities introduced in Nijhout and Reed (Integr Comp Biol 54(2):264–275, 2014. https://doi.org/10.1093/icb/icu010) and Nijhout et al. (Math Biosci 257:104–110, 2014). See Golubitsky and Stewart (2017). The first two of these mechanisms are illustrated by feedforward excitation and substrate inhibition. Structural homeostasis occurs only when the network has a feedforward loop as a subnetwork; that is, when there are two distinct simple paths connecting the input node to the output node. Moreover, when the network is just the feedforward loop motif itself, one of the paths must be excitatory and one inhibitory to support infinitesimal homeostasis. Haldane homeostasis occurs when there is a single simple path from the input node to the output node and then only when one of the couplings along this path has strength 0. Null-degradation homeostasis is illustrated by a biochemical example from Ma et al. (2009); this kind of homeostasis can occur only when the degradation constant of the third node is 0. The paper ends with an analysis of Haldane homeostasis infinitesimal chair singularities.

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Notes

  1. See http://www.people.vcu.edu/~gasmerom/MAT131/graphs.html.

  2. We thank Mike Reed for suggesting the term structural homeostasis.

  3. See the Online Encyclopedia of Integer Sequences at http://oeis.org/A003085.

References

  • Ang J, McMillen DR (2013) Physical constraints on biological integral control design for homeostasis and sensory adaptation. Biophys J 104(2):505–515

    Article  Google Scholar 

  • Antoneli F, Golubitsky M, Stewart I (2018) Homeostasis in a feed forward loop gene regulatory network motif. J Theor Biol 445:103–109. https://doi.org/10.1016/j.jtbi.2018.02.026

    Article  MATH  Google Scholar 

  • Aoki SK, Lillacci G, Gupta A, Baumschlager A, Schweingruber D, Khammash M (2019) A universal biomolecular integral feedback controller for robust perfect adaptation. Nature 570:533–537

    Article  Google Scholar 

  • Del Vecchio D, Qian Y, Murray RM, Sontag ED (2018) Annual reviews in control future systems and control research in synthetic biology. Annu Rev Control 45:5–17

    Article  MathSciNet  Google Scholar 

  • Ferrell JE (2016) Perfect and near perfect adaptation in cell signaling. Cell Syst 2:62–67

    Article  Google Scholar 

  • Golubitsky M, Stewart I (2006) Nonlinear dynamics of networks: the groupoid formalism. Bull Am Math Soc 43:305–364

    Article  MathSciNet  Google Scholar 

  • Golubitsky M, Stewart I (2017) Homeostasis, singularities and networks. J Math Biol 74:387–407

    Article  MathSciNet  Google Scholar 

  • Golubitsky M, Stewart I (2018) Homeostasis with multiple inputs. SIAM J Appl Dyn Syst 17(2):1816–1832

    Article  MathSciNet  Google Scholar 

  • Haldane J (1930) Enzymes. Longmans, Green, and Co, New York

    Google Scholar 

  • Ma W, Trusina A, El-Samad H, Lim WA, Tang C (2009) Defining network topologies that can achieve biochemical adaptation. Cell 138:760–773

    Article  Google Scholar 

  • Nijhout HF, Reed MC (2014) Homeostasis and dynamic stability of the phenotype link robustness and plasticity. Integr Comp Biol 54(2):264–275. https://doi.org/10.1093/icb/icu010

    Article  Google Scholar 

  • Nijhout HF, Reed MC, Budu P, Ulrich CM (2004) A mathematical model of the folate cycle: new insights into folate homeostasis. J Biol Chem 279:55008–55016

    Article  Google Scholar 

  • Nijhout HF, Best J, Reed M (2014) Escape from homeostasis. Math Biosci 257:104–110

    Article  MathSciNet  Google Scholar 

  • Nijhout HF, Best JA, Reed MC (2015) Using mathematical models to understand metabolism, genes and disease. BMC Biol 13:79

    Article  Google Scholar 

  • Nijhout HF, Best J, Reed MC (2018) Systems biology of robustness and homeostatic mechanisms. Wiley Interdiscip Rev Syst Biol Med 11:e1440

    Article  Google Scholar 

  • Qian Y, Del Vecchio D (2018) Realizing ’integral control’ in living cells: how to overcome leaky integration due to dilution? J R Soc Interface 15(139):20170902

    Article  Google Scholar 

  • Reed MC, Lieb A, Nijhout HF (2010) The biological significance of substrate inhibition: a mechanism with diverse functions. BioEssays 32(5):422–429

    Article  Google Scholar 

  • Reed M, Best J, Golubitsky M, Stewart I, Nijhout HF (2017) Analysis of homeostatic mechanisms in biochemical networks. Bull Math Biol 79(9):1–24

    MathSciNet  MATH  Google Scholar 

  • Tang ZF, McMillen DR (2016) Design principles for the analysis and construction of robustly homeostatic biological networks. J Theor Biol 408:274–289

    Article  MathSciNet  Google Scholar 

  • Tyson JJ, Novak B (2010) Functional motifs in biochemical reaction networks. Annu Rev Phys Chem 61:219–240

    Article  Google Scholar 

Download references

Acknowledgements

We thank Janet Best, Tony Nance, Mike Reed, and Ian Stewart for helpful conversations. We also thank the reviewers for making a number of suggestions that greatly improved the paper. This research was supported by the National Science Foundation Grant DMS-1440386 to the Mathematical Biosciences Institute. In particular, YW was in residence at MBI when much of this research was completed.

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Correspondence to Martin Golubitsky.

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Golubitsky, M., Wang, Y. Infinitesimal homeostasis in three-node input–output networks. J. Math. Biol. 80, 1163–1185 (2020). https://doi.org/10.1007/s00285-019-01457-x

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