TY - JOUR
T1 - The sensitivity of Turing self-organization to biological feedback delays: 2D models of fish pigmentation
AU - Gaffney, E. A.
AU - Lee, S. S.
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledged KAUST grant number(s): KUK-C1-013-04
Acknowledgements: This publication is based on work supported in part by Award No. KUK-C1-013-04, made by King Abdullah University of Science and Technology (KAUST) and Grant-in-Aid for JSPS Young Research Fellow from The Japan Society for The Promotion of Science (JSPS).
This publication acknowledges KAUST support, but has no KAUST affiliated authors.
PY - 2013/10/1
Y1 - 2013/10/1
N2 - © The authors 2013. Turing morphogen models have been extensively explored in the context of large-scale self-organization in multicellular biological systems. However, reconciling the detailed biology of morphogen dynamics, while accounting for time delays associated with gene expression, reveals aberrant behaviours that are not consistent with early developmental self-organization, especially the requirement for exquisite temporal control. Attempts to reconcile the interpretation of Turing's ideas with an increasing understanding of the mechanisms driving zebrafish pigmentation suggests that one should reconsider Turing's model in terms of pigment cells rather than morphogens (Nakamasu et al., 2009, PNAS, 106, 8429-8434; Yamaguchi et al., 2007, PNAS, 104, 4790-4793). Here the dynamics of pigment cells is subject to response delays implicit in the cell cycle and apoptosis. Hence we explore simulations of fish skin patterning, focussing on the dynamical influence of gene expression delays in morphogen-based Turing models and response delays for cell-based Turing models. We find that reconciling the mechanisms driving the behaviour of Turing systems with observations of fish skin patterning remains a fundamental challenge.
AB - © The authors 2013. Turing morphogen models have been extensively explored in the context of large-scale self-organization in multicellular biological systems. However, reconciling the detailed biology of morphogen dynamics, while accounting for time delays associated with gene expression, reveals aberrant behaviours that are not consistent with early developmental self-organization, especially the requirement for exquisite temporal control. Attempts to reconcile the interpretation of Turing's ideas with an increasing understanding of the mechanisms driving zebrafish pigmentation suggests that one should reconsider Turing's model in terms of pigment cells rather than morphogens (Nakamasu et al., 2009, PNAS, 106, 8429-8434; Yamaguchi et al., 2007, PNAS, 104, 4790-4793). Here the dynamics of pigment cells is subject to response delays implicit in the cell cycle and apoptosis. Hence we explore simulations of fish skin patterning, focussing on the dynamical influence of gene expression delays in morphogen-based Turing models and response delays for cell-based Turing models. We find that reconciling the mechanisms driving the behaviour of Turing systems with observations of fish skin patterning remains a fundamental challenge.
UR - http://hdl.handle.net/10754/599961
UR - https://academic.oup.com/imammb/article-lookup/doi/10.1093/imammb/dqt017
UR - http://www.scopus.com/inward/record.url?scp=84925431437&partnerID=8YFLogxK
U2 - 10.1093/imammb/dqt017
DO - 10.1093/imammb/dqt017
M3 - Article
C2 - 24087834
SN - 1477-8599
VL - 32
SP - 57
EP - 79
JO - Mathematical Medicine and Biology
JF - Mathematical Medicine and Biology
IS - 1
ER -