Spatiotemporal development of coexisting wave domains of Rho activity in the cell cortex
Abstract The Rho family GTPases are molecular switches that regulate cytoskeletal dynamics and cell movement through a complex spatiotemporal organization of their activity. In Patiria miniata (starfish) oocytes under in vitro experimental conditions (with overexpressed Ect2, induced expression of Δ...
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2021-09-01
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doaj-ac93049fb393468f99e8ce7da81df15b2021-10-03T11:30:07ZengNature Publishing GroupScientific Reports2045-23222021-09-0111111910.1038/s41598-021-99029-xSpatiotemporal development of coexisting wave domains of Rho activity in the cell cortexSiarhei Hladyshau0Mary Kho1Shuyi Nie2Denis Tsygankov3School of Biology, Georgia Institute of TechnologySchool of Biology, Georgia Institute of TechnologySchool of Biology, Georgia Institute of TechnologyWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory UniversityAbstract The Rho family GTPases are molecular switches that regulate cytoskeletal dynamics and cell movement through a complex spatiotemporal organization of their activity. In Patiria miniata (starfish) oocytes under in vitro experimental conditions (with overexpressed Ect2, induced expression of Δ90 cyclin B, and roscovitine treatment), such activity generates multiple co-existing regions of coherent propagation of actin waves. Here we use computational modeling to investigate the development and properties of such wave domains. The model reveals that the formation of wave domains requires a balance between the activation and inhibition in the Rho signaling motif. Intriguingly, the development of the wave domains is preceded by a stage of low-activity quasi-static patterns, which may not be readily observed in experiments. Spatiotemporal patterns of this stage and the different paths of their destabilization define the behavior of the system in the later high-activity (observable) stage. Accounting for a strong intrinsic noise allowed us to achieve good quantitative agreement between simulated dynamics in different parameter regimes of the model and different wave dynamics in Patiria miniata and wild type Xenopus laevis (frog) data. For quantitative comparison of simulated and experimental results, we developed an automated method of wave domain detection, which revealed a sharp reversal in the process of pattern formation in starfish oocytes. Overall, our findings provide an insight into spatiotemporal regulation of complex and diverse but still computationally reproducible cell-level actin dynamics.https://doi.org/10.1038/s41598-021-99029-x |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Siarhei Hladyshau Mary Kho Shuyi Nie Denis Tsygankov |
spellingShingle |
Siarhei Hladyshau Mary Kho Shuyi Nie Denis Tsygankov Spatiotemporal development of coexisting wave domains of Rho activity in the cell cortex Scientific Reports |
author_facet |
Siarhei Hladyshau Mary Kho Shuyi Nie Denis Tsygankov |
author_sort |
Siarhei Hladyshau |
title |
Spatiotemporal development of coexisting wave domains of Rho activity in the cell cortex |
title_short |
Spatiotemporal development of coexisting wave domains of Rho activity in the cell cortex |
title_full |
Spatiotemporal development of coexisting wave domains of Rho activity in the cell cortex |
title_fullStr |
Spatiotemporal development of coexisting wave domains of Rho activity in the cell cortex |
title_full_unstemmed |
Spatiotemporal development of coexisting wave domains of Rho activity in the cell cortex |
title_sort |
spatiotemporal development of coexisting wave domains of rho activity in the cell cortex |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-09-01 |
description |
Abstract The Rho family GTPases are molecular switches that regulate cytoskeletal dynamics and cell movement through a complex spatiotemporal organization of their activity. In Patiria miniata (starfish) oocytes under in vitro experimental conditions (with overexpressed Ect2, induced expression of Δ90 cyclin B, and roscovitine treatment), such activity generates multiple co-existing regions of coherent propagation of actin waves. Here we use computational modeling to investigate the development and properties of such wave domains. The model reveals that the formation of wave domains requires a balance between the activation and inhibition in the Rho signaling motif. Intriguingly, the development of the wave domains is preceded by a stage of low-activity quasi-static patterns, which may not be readily observed in experiments. Spatiotemporal patterns of this stage and the different paths of their destabilization define the behavior of the system in the later high-activity (observable) stage. Accounting for a strong intrinsic noise allowed us to achieve good quantitative agreement between simulated dynamics in different parameter regimes of the model and different wave dynamics in Patiria miniata and wild type Xenopus laevis (frog) data. For quantitative comparison of simulated and experimental results, we developed an automated method of wave domain detection, which revealed a sharp reversal in the process of pattern formation in starfish oocytes. Overall, our findings provide an insight into spatiotemporal regulation of complex and diverse but still computationally reproducible cell-level actin dynamics. |
url |
https://doi.org/10.1038/s41598-021-99029-x |
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