TY - JOUR
T1 - Identifying (un)controllable dynamical behavior in complex networks
AU - Rozum, Jordan C.
AU - Albert, Réka
N1 - Funding Information:
This work was funded by NSF grants PHY 1205840 and PHY 1545832 to RA. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We thank Jorge Zañudo for his helpful insights and conversations.
Publisher Copyright:
© 2018 Rozum, Albert. http://creativecommons.org/licenses/by/4.0/.
PY - 2018/12
Y1 - 2018/12
N2 - We present a technique applicable in any dynamical framework to identify control-robust subsets of an interacting system. These robust subsystems, which we call stable modules, are characterized by constraints on the variables that make up the subsystem. They are robust in the sense that if the defining constraints are satisfied at a given time, they remain satisfied for all later times, regardless of what happens in the rest of the system, and can only be broken if the constrained variables are externally manipulated. We identify stable modules as graph structures in an expanded network, which represents causal links between variable constraints. A stable module represents a system “decision point”, or trap subspace. Using the expanded network, small stable modules can be composed sequentially to form larger stable modules that describe dynamics on the system level. Collections of large, mutually exclusive stable modules describe the system’s repertoire of long-term behaviors. We implement this technique in a broad class of dynamical systems and illustrate its practical utility via examples and algorithmic analysis of two published biological network models. In the segment polarity gene network of Drosophila melanogaster, we obtain a state-space visualization that reproduces by novel means the four possible cell fates and predicts the outcome of cell transplant experiments. In the T-cell signaling network, we identify six signaling elements that determine the high-signal response and show that control of an element connected to them cannot disrupt this response.
AB - We present a technique applicable in any dynamical framework to identify control-robust subsets of an interacting system. These robust subsystems, which we call stable modules, are characterized by constraints on the variables that make up the subsystem. They are robust in the sense that if the defining constraints are satisfied at a given time, they remain satisfied for all later times, regardless of what happens in the rest of the system, and can only be broken if the constrained variables are externally manipulated. We identify stable modules as graph structures in an expanded network, which represents causal links between variable constraints. A stable module represents a system “decision point”, or trap subspace. Using the expanded network, small stable modules can be composed sequentially to form larger stable modules that describe dynamics on the system level. Collections of large, mutually exclusive stable modules describe the system’s repertoire of long-term behaviors. We implement this technique in a broad class of dynamical systems and illustrate its practical utility via examples and algorithmic analysis of two published biological network models. In the segment polarity gene network of Drosophila melanogaster, we obtain a state-space visualization that reproduces by novel means the four possible cell fates and predicts the outcome of cell transplant experiments. In the T-cell signaling network, we identify six signaling elements that determine the high-signal response and show that control of an element connected to them cannot disrupt this response.
UR - http://www.scopus.com/inward/record.url?scp=85058918600&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85058918600&partnerID=8YFLogxK
U2 - 10.1371/journal.pcbi.1006630
DO - 10.1371/journal.pcbi.1006630
M3 - Article
C2 - 30532150
AN - SCOPUS:85058918600
SN - 1553-734X
VL - 14
JO - PLoS Computational Biology
JF - PLoS Computational Biology
IS - 12
M1 - e1006630
ER -