System identification of signaling dependent gene expression with different time-scale data

PLoS Comput Biol. 2017 Dec 27;13(12):e1005913. doi: 10.1371/journal.pcbi.1005913. eCollection 2017 Dec.

Abstract

Cells decode information of signaling activation at a scale of tens of minutes by downstream gene expression with a scale of hours to days, leading to cell fate decisions such as cell differentiation. However, no system identification method with such different time scales exists. Here we used compressed sensing technology and developed a system identification method using data of different time scales by recovering signals of missing time points. We measured phosphorylation of ERK and CREB, immediate early gene expression products, and mRNAs of decoder genes for neurite elongation in PC12 cell differentiation and performed system identification, revealing the input-output relationships between signaling and gene expression with sensitivity such as graded or switch-like response and with time delay and gain, representing signal transfer efficiency. We predicted and validated the identified system using pharmacological perturbation. Thus, we provide a versatile method for system identification using data with different time scales.

Publication types

  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Computational Biology
  • Cyclic AMP Response Element-Binding Protein / metabolism
  • Gene Expression*
  • Kinetics
  • MAP Kinase Signaling System
  • Models, Biological
  • Neurites / metabolism
  • PC12 Cells
  • Rats
  • Signal Transduction*
  • Systems Biology

Substances

  • Cyclic AMP Response Element-Binding Protein

Grants and funding

This work was supported by the Creation of Fundamental Technologies for Understanding and Control of Biosystem Dynamics, CREST, of the Japan Science and Technology Agency (JST) (#JPMJCR12W3, http://www.jst.go.jp/kisoken/crest/en/index.html), and a Grant-in-Aid for Scientific Research on Innovative Areas (#17H06300, #17H06299, http://www.jsps.go.jp/english/e-grants/index.html). TT receives funding from a Grant-in-Aid for Japan Society for the Promotion of Science (JSPS) Research Fellow (#14J12344, http://www.jsps.go.jp/english/e-grants/index.html). MF receives funding from a Grant-in-Aid for Challenging Exploratory Research (#16K12508, http://www.jsps.go.jp/english/e-grants/index.html). KKu receives funding from a Grant-in-Aid for Young Scientists (B) (#16K19028, http://www.jsps.go.jp/english/e-grants/index.html). SU receives funding from a Grant-in-Aid for Scientific Research on Innovative Areas (#16H01551, http://www.jsps.go.jp/english/e-grants/index.html). HK receives funding from a Grant-in-Aid for Scientific Research on Innovative Areas (#16H06577, http://www.jsps.go.jp/english/e-grants/index.html). KKo receives funding from a Grant-in-Aid for Scientific Research (B) (#15KT0021, http://www.jsps.go.jp/english/e-grants/index.html), and (C) (#15K00246, http://www.jsps.go.jp/english/e-grants/index.html), and Grant-in-Aid for Scientific Research on Innovative Areas (#16H01554, http://www.jsps.go.jp/english/e-grants/index.html). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.