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Synthetic Lateral Inhibition in Periodic Pattern Forming Microbial Colonies
[Image: see text] Multicellular entities are characterized by intricate spatial patterns, intimately related to the functions they perform. These patterns are often created from isotropic embryonic structures, without external information cues guiding the symmetry breaking process. Mature biological...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486170/ https://www.ncbi.nlm.nih.gov/pubmed/33449631 http://dx.doi.org/10.1021/acssynbio.0c00318 |
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author | Duran-Nebreda, Salva Pla, Jordi Vidiella, Blai Piñero, Jordi Conde-Pueyo, Nuria Solé, Ricard |
author_facet | Duran-Nebreda, Salva Pla, Jordi Vidiella, Blai Piñero, Jordi Conde-Pueyo, Nuria Solé, Ricard |
author_sort | Duran-Nebreda, Salva |
collection | PubMed |
description | [Image: see text] Multicellular entities are characterized by intricate spatial patterns, intimately related to the functions they perform. These patterns are often created from isotropic embryonic structures, without external information cues guiding the symmetry breaking process. Mature biological structures also display characteristic scales with repeating distributions of signals or chemical species across space. Many candidate patterning modules have been used to explain processes during development and typically include a set of interacting and diffusing chemicals or agents known as morphogens. Great effort has been put forward to better understand the conditions in which pattern-forming processes can occur in the biological domain. However, evidence and practical knowledge allowing us to engineer symmetry-breaking is still lacking. Here we follow a different approach by designing a synthetic gene circuit in E. coli that implements a local activation long-range inhibition mechanism. The synthetic gene network implements an artificial differentiation process that changes the physicochemical properties of the agents. Using both experimental results and modeling, we show that the proposed system is capable of symmetry-breaking leading to regular spatial patterns during colony growth. Studying how these patterns emerge is fundamental to further our understanding of the evolution of biocomplexity and the role played by self-organization. The artificial system studied here and the engineering perspective on embryogenic processes can help validate developmental theories and identify universal properties underpinning biological pattern formation, with special interest for the area of synthetic developmental biology. |
format | Online Article Text |
id | pubmed-8486170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-84861702021-10-04 Synthetic Lateral Inhibition in Periodic Pattern Forming Microbial Colonies Duran-Nebreda, Salva Pla, Jordi Vidiella, Blai Piñero, Jordi Conde-Pueyo, Nuria Solé, Ricard ACS Synth Biol [Image: see text] Multicellular entities are characterized by intricate spatial patterns, intimately related to the functions they perform. These patterns are often created from isotropic embryonic structures, without external information cues guiding the symmetry breaking process. Mature biological structures also display characteristic scales with repeating distributions of signals or chemical species across space. Many candidate patterning modules have been used to explain processes during development and typically include a set of interacting and diffusing chemicals or agents known as morphogens. Great effort has been put forward to better understand the conditions in which pattern-forming processes can occur in the biological domain. However, evidence and practical knowledge allowing us to engineer symmetry-breaking is still lacking. Here we follow a different approach by designing a synthetic gene circuit in E. coli that implements a local activation long-range inhibition mechanism. The synthetic gene network implements an artificial differentiation process that changes the physicochemical properties of the agents. Using both experimental results and modeling, we show that the proposed system is capable of symmetry-breaking leading to regular spatial patterns during colony growth. Studying how these patterns emerge is fundamental to further our understanding of the evolution of biocomplexity and the role played by self-organization. The artificial system studied here and the engineering perspective on embryogenic processes can help validate developmental theories and identify universal properties underpinning biological pattern formation, with special interest for the area of synthetic developmental biology. American Chemical Society 2021-01-15 2021-02-19 /pmc/articles/PMC8486170/ /pubmed/33449631 http://dx.doi.org/10.1021/acssynbio.0c00318 Text en © 2021 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Duran-Nebreda, Salva Pla, Jordi Vidiella, Blai Piñero, Jordi Conde-Pueyo, Nuria Solé, Ricard Synthetic Lateral Inhibition in Periodic Pattern Forming Microbial Colonies |
title | Synthetic Lateral Inhibition in Periodic Pattern Forming
Microbial Colonies |
title_full | Synthetic Lateral Inhibition in Periodic Pattern Forming
Microbial Colonies |
title_fullStr | Synthetic Lateral Inhibition in Periodic Pattern Forming
Microbial Colonies |
title_full_unstemmed | Synthetic Lateral Inhibition in Periodic Pattern Forming
Microbial Colonies |
title_short | Synthetic Lateral Inhibition in Periodic Pattern Forming
Microbial Colonies |
title_sort | synthetic lateral inhibition in periodic pattern forming
microbial colonies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486170/ https://www.ncbi.nlm.nih.gov/pubmed/33449631 http://dx.doi.org/10.1021/acssynbio.0c00318 |
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