Skip to main content

Stochastic Modular Analysis for Gene Circuits: Interplay Among Retroactivity, Nonlinearity, and Stochasticity

  • Protocol
  • First Online:

Part of the book series: Methods in Molecular Biology ((MIMB,volume 1244))

Abstract

This chapter introduces a computational analysis method for analyzing gene circuit dynamics in terms of modules while taking into account stochasticity, system nonlinearity, and retroactivity.

  1. (1)

    Analog electrical circuit representation for gene circuits: A connection between two gene circuit components is often mediated by a transcription factor (TF) and the connection signal is described by the TF concentration. The TF is sequestered to its specific binding site (promoter region) and regulates downstream transcription. This sequestration has been known to affect the dynamics of the TF by increasing its response time. The downstream effect—retroactivity—has been shown to be explicitly described in an electrical circuit representation, as an input capacitance increase. We provide a brief review on this topic.

  2. (2)

    Modular description of noise propagation: Gene circuit signals are noisy due to the random nature of biological reactions. The noisy fluctuations in TF concentrations affect downstream regulation. Thus, noise can propagate throughout the connected system components. This can cause different circuit components to behave in a statistically dependent manner, hampering a modular analysis. Here, we show that the modular analysis is still possible at the linear noise approximation level.

  3. (3)

    Noise effect on module input–output response: We investigate how to deal with a module input–output response and its noise dependency. Noise-induced phenotypes are described as an interplay between system nonlinearity and signal noise.

Lastly, we provide the comprehensive approach incorporating the above three analysis methods, which we call “stochastic modular analysis.” This method can provide an analysis framework for gene circuit dynamics when the nontrivial effects of retroactivity, stochasticity, and nonlinearity need to be taken into account.

This is a preview of subscription content, log in via an institution.

Buying options

eBook
USD   39.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD   54.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

Springer Nature is developing a new tool to find and evaluate Protocols. Learn more

References

  1. Baldwin CY, Clark KB (2000) Design rules: the power of modularity. MIT Press, Cambridge

    Google Scholar 

  2. Kim KH, Sauro HM (2010) Fan-out in gene regulatory networks. J Biol Eng 4:16

    Article  PubMed Central  PubMed  Google Scholar 

  3. Jiang P, Ventura AC, Sontag ED, Merajver SD, Ninfa AJ, Del Vecchio D (2011) Load-induced modulation of signal transduction networks. Sci Signal 4(194):ra67

    Google Scholar 

  4. Ventura AC, Jiang P, Van Wassenhove L, Del Vecchio D, Merajver SD, Ninfa AJ (2010) Signaling properties of a covalent modification cycle are altered by a downstream target. Proc Natl Acad Sci USA 107:10032–10037

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  5. Buchler NE, Cross FR (2009) Protein sequestration generates a flexible ultrasensitive response in a genetic network. Mol Syst Biol 5:272

    Article  PubMed Central  PubMed  Google Scholar 

  6. Jayanthi S, Nilgiriwala KS, Del Vecchio D (2013) Retroactivity controls the temporal dynamics of gene transcription. ACS Synth Biol

    Google Scholar 

  7. Daniel R, Rubens JR, Sarpeshkar R, Lu TK (2013) Synthetic analog computation in living cells. Nature 497(7451):619–623

    Article  CAS  PubMed  Google Scholar 

  8. Del Vecchio D, Ninfa AJ, Sontag ED (2008) Modular cell biology: retroactivity and insulation. Mol Syst Biol 4:161

    PubMed Central  PubMed  Google Scholar 

  9. Weinberger LS, Dar RD, Simpson ML (2008) Transient-mediated fate determination in a transcriptional circuit of HIV. Nat Genet 40(4):466–470

    Article  CAS  PubMed  Google Scholar 

  10. Kim KH, Sauro HM (2011) Measuring retroactivity from noise in gene regulatory networks. Biophys J 100(5):1167–1177

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  11. Kim KH, Sauro HM (2012) Measuring the degree of modularity in gene regulatory networks from the relaxation of finite perturbations. In: 2012 I.E. 51st IEEE conference on decision and control (CDC), pp 5330–5335

    Google Scholar 

  12. Elf J, Ehrenberg M (2003) Fast evaluation of fluctuations in biochemical networks with the linear noise approximation. Genome Res 13(11):2475–2484

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  13. Paulsson J (2004) Summing up the noise in gene networks. Nature 427(6973):415–418

    Article  CAS  PubMed  Google Scholar 

  14. Tănase-Nicola S, Warren PB, ten Wolde PR (2006) Signal detection, modularity, and the correlation between extrinsic and intrinsic noise in biochemical networks. Phys Rev Lett 97(6):68102

    Article  Google Scholar 

  15. Warren PB, Tanase-Nicola S, ten Wolde PR (2006) Exact results for noise power spectra in linear biochemical reaction networks. J Chem Phys 125(14):144904

    Article  PubMed  Google Scholar 

  16. Kwakernaak H, Sivan R (1972) Linear optimal control systems. Wiley-Interscience, New York

    Google Scholar 

  17. Simpson ML, Cox CD, Sayler GS (2003) Frequency domain analysis of noise in autoregulated gene circuits. Proc Natl Acad Sci USA 100(8):4551

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  18. Austin DW, Allen MS, McCollum JM, Dar RD, Wilgus JR, Sayler GS, Samatova NF, Cox CD, Simpson ML (2006) Gene network shaping of inherent noise spectra. Nature 439:608–611

    Article  CAS  PubMed  Google Scholar 

  19. Paulsson J, Berg OG, Ehrenberg M (2000) Stochastic focusing: fluctuation-enhanced sensitivity of intracellular regulation. Proc Natl Acad Sci USA 97(13):7148–7153

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  20. Kim KH, Qian H, Sauro HM (2013) Nonlinear biochemical signal processing via noise propagation. arXiv:1309.2588 [q-bio.QM]

    Google Scholar 

  21. Gómez-Uribe CA, Verghese GC (2007) Mass fluctuation kinetics: capturing stochastic effects in systems of chemical reactions through coupled mean-variance computations. J Chem Phys 126(2):24109

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Kyung Hyuk Kim .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2015 Springer Science+Business Media New York

About this protocol

Cite this protocol

Kim, K.H., Sauro, H.M. (2015). Stochastic Modular Analysis for Gene Circuits: Interplay Among Retroactivity, Nonlinearity, and Stochasticity. In: Marchisio, M. (eds) Computational Methods in Synthetic Biology. Methods in Molecular Biology, vol 1244. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-1878-2_14

Download citation

  • DOI: https://doi.org/10.1007/978-1-4939-1878-2_14

  • Published:

  • Publisher Name: Humana Press, New York, NY

  • Print ISBN: 978-1-4939-1877-5

  • Online ISBN: 978-1-4939-1878-2

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics