TY - GEN
T1 - The Relationship between microscopic and collective properties in gene regulatory network-based morphogenetic systems
AU - Kim, Hyobin
AU - Sayama, Hiroki
N1 - Funding Information:
This material is based upon work supported by the US National Science Foundation under Grant No. 1319152.
Publisher Copyright:
© 2016 MIT Press. All rights reserved.
PY - 2016
Y1 - 2016
N2 - Gene regulatory network (GRN)-based morphogenetic systems have recently attracted an increasing attention in artificial life and morphogenetic engineering research. However, the relationship between microscopic properties of intracellular GRNs and collective properties of morphogenetic systems has not been fully explored yet. Thus, we propose a new GRN-based framework to elucidate how critical dynamics of GRNs in individual cells affect cell fates such as proliferation, apoptosis, and differentiation in resulting morphogenetic systems. Our model represents an aggregation of cells, where each cell has a GRN in it. We used Kauffman's NK Boolean networks for GRNs. Specifically, we randomly assigned three cell fates to the attractors. Varying the properties of GRNs from ordered, through critical, to chaotic regimes, we observed the process that cells are aggregated. We found that the criticality of a GRN made an optimal partition of basins of attraction, which led to a maximum balance between cell fates. Based on the result, we can conclude that the criticality of a GRN is an important controller to determine the frequencies of cell fates in morphogenetic systems.
AB - Gene regulatory network (GRN)-based morphogenetic systems have recently attracted an increasing attention in artificial life and morphogenetic engineering research. However, the relationship between microscopic properties of intracellular GRNs and collective properties of morphogenetic systems has not been fully explored yet. Thus, we propose a new GRN-based framework to elucidate how critical dynamics of GRNs in individual cells affect cell fates such as proliferation, apoptosis, and differentiation in resulting morphogenetic systems. Our model represents an aggregation of cells, where each cell has a GRN in it. We used Kauffman's NK Boolean networks for GRNs. Specifically, we randomly assigned three cell fates to the attractors. Varying the properties of GRNs from ordered, through critical, to chaotic regimes, we observed the process that cells are aggregated. We found that the criticality of a GRN made an optimal partition of basins of attraction, which led to a maximum balance between cell fates. Based on the result, we can conclude that the criticality of a GRN is an important controller to determine the frequencies of cell fates in morphogenetic systems.
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M3 - Conference contribution
AN - SCOPUS:85087105351
T3 - Proceedings of the Artificial Life Conference 2016, ALIFE 2016
BT - Proceedings of the Artificial Life Conference 2016, ALIFE 2016
A2 - Gershenson, Carlos
A2 - Froese, Tom
A2 - Siqueiros, Jesus M.
A2 - Aguilar, Wendy
A2 - Izquierdo, Eduardo J.
A2 - Hiroki, Sayama
PB - MIT Press Journals
T2 - 15th International Conference on the Synthesis and Simulation of Living Systems, ALIFE 2016
Y2 - 4 July 2016 through 8 July 2016
ER -