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Landscape reveals critical network structures for sharpening gene expression boundaries

BACKGROUND: Spatial pattern formation is a critical issue in developmental biology. Gene expression boundary sharpening has been observed from both experiments and modeling simulations. However, the mechanism to determine the sharpness of the boundary is not fully elucidated. RESULTS: We investigate...

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Autores principales: Li, Chunhe, Zhang, Lei, Nie, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001026/
https://www.ncbi.nlm.nih.gov/pubmed/29898720
http://dx.doi.org/10.1186/s12918-018-0595-5
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author Li, Chunhe
Zhang, Lei
Nie, Qing
author_facet Li, Chunhe
Zhang, Lei
Nie, Qing
author_sort Li, Chunhe
collection PubMed
description BACKGROUND: Spatial pattern formation is a critical issue in developmental biology. Gene expression boundary sharpening has been observed from both experiments and modeling simulations. However, the mechanism to determine the sharpness of the boundary is not fully elucidated. RESULTS: We investigated the boundary sharpening resulted by three biological motifs, interacting with morphogens, and uncovered their probabilistic landscapes. The landscape view, along with calculated average switching time between attractors, provides a natural explanation for the boundary sharpening behavior relying on the noise induced gene state switchings. To possess boundary sharpening potential, a gene network needs to generate an asymmetric bistable state, i.e. one of the two stable states is less stable than the other. We found that the mutual repressed self-activation model displays more robust boundary sharpening ability against parameter perturbation, compared to the mutual repression or the self-activation model. This is supported by the results of switching time calculated from the landscape, which indicate that the mutual repressed self-activation model has shortest switching time, among three models. Additionally, introducing cross gradients of morphogens provides a more stable mechanism for the boundary sharpening of gene expression, due to a two-way switching mechanism. CONCLUSIONS: Our results reveal the underlying principle for the gene expression boundary sharpening, and pave the way for the mechanistic understanding of cell fate decisions in the pattern formation processes of development. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-018-0595-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-60010262018-06-26 Landscape reveals critical network structures for sharpening gene expression boundaries Li, Chunhe Zhang, Lei Nie, Qing BMC Syst Biol Research Article BACKGROUND: Spatial pattern formation is a critical issue in developmental biology. Gene expression boundary sharpening has been observed from both experiments and modeling simulations. However, the mechanism to determine the sharpness of the boundary is not fully elucidated. RESULTS: We investigated the boundary sharpening resulted by three biological motifs, interacting with morphogens, and uncovered their probabilistic landscapes. The landscape view, along with calculated average switching time between attractors, provides a natural explanation for the boundary sharpening behavior relying on the noise induced gene state switchings. To possess boundary sharpening potential, a gene network needs to generate an asymmetric bistable state, i.e. one of the two stable states is less stable than the other. We found that the mutual repressed self-activation model displays more robust boundary sharpening ability against parameter perturbation, compared to the mutual repression or the self-activation model. This is supported by the results of switching time calculated from the landscape, which indicate that the mutual repressed self-activation model has shortest switching time, among three models. Additionally, introducing cross gradients of morphogens provides a more stable mechanism for the boundary sharpening of gene expression, due to a two-way switching mechanism. CONCLUSIONS: Our results reveal the underlying principle for the gene expression boundary sharpening, and pave the way for the mechanistic understanding of cell fate decisions in the pattern formation processes of development. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-018-0595-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-13 /pmc/articles/PMC6001026/ /pubmed/29898720 http://dx.doi.org/10.1186/s12918-018-0595-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Li, Chunhe
Zhang, Lei
Nie, Qing
Landscape reveals critical network structures for sharpening gene expression boundaries
title Landscape reveals critical network structures for sharpening gene expression boundaries
title_full Landscape reveals critical network structures for sharpening gene expression boundaries
title_fullStr Landscape reveals critical network structures for sharpening gene expression boundaries
title_full_unstemmed Landscape reveals critical network structures for sharpening gene expression boundaries
title_short Landscape reveals critical network structures for sharpening gene expression boundaries
title_sort landscape reveals critical network structures for sharpening gene expression boundaries
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001026/
https://www.ncbi.nlm.nih.gov/pubmed/29898720
http://dx.doi.org/10.1186/s12918-018-0595-5
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