Cargando…

Evolution of selfish multicellularity: collective organisation of individual spatio-temporal regulatory strategies

BACKGROUND: The unicellular ancestors of modern-day multicellular organisms were remarkably complex. They had an extensive set of regulatory and signalling genes, an intricate life cycle and could change their behaviour in response to environmental changes. At the transition to multicellularity, som...

Descripción completa

Detalles Bibliográficos
Autores principales: Vroomans, Renske M. A., Colizzi, Enrico Sandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357660/
https://www.ncbi.nlm.nih.gov/pubmed/37468829
http://dx.doi.org/10.1186/s12862-023-02133-x
_version_ 1785075541706014720
author Vroomans, Renske M. A.
Colizzi, Enrico Sandro
author_facet Vroomans, Renske M. A.
Colizzi, Enrico Sandro
author_sort Vroomans, Renske M. A.
collection PubMed
description BACKGROUND: The unicellular ancestors of modern-day multicellular organisms were remarkably complex. They had an extensive set of regulatory and signalling genes, an intricate life cycle and could change their behaviour in response to environmental changes. At the transition to multicellularity, some of these behaviours were co-opted to organise the development of the nascent multicellular organism. Here, we focus on the transition to multicellularity before the evolution of stable cell differentiation, to reveal how the emergence of clusters affects the evolution of cell behaviour. RESULTS: We construct a computational model of a population of cells that can evolve the regulation of their behavioural state - either division or migration - and study both a unicellular and a multicellular context. Cells compete for reproduction and for resources to survive in a seasonally changing environment. We find that the evolution of multicellularity strongly determines the co-evolution of cell behaviour, by altering the competition dynamics between cells. When adhesion cannot evolve, cells compete for survival by rapidly migrating towards resources before dividing. When adhesion evolves, emergent collective migration alleviates the pressure on individual cells to reach resources. This allows individual cells to maximise their own replication. Migrating adhesive clusters display striking patterns of spatio-temporal cell state changes that visually resemble animal development. CONCLUSIONS: Our model demonstrates how emergent selection pressures at the onset of multicellularity can drive the evolution of cellular behaviour to give rise to developmental patterns. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12862-023-02133-x.
format Online
Article
Text
id pubmed-10357660
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-103576602023-07-21 Evolution of selfish multicellularity: collective organisation of individual spatio-temporal regulatory strategies Vroomans, Renske M. A. Colizzi, Enrico Sandro BMC Ecol Evol Research BACKGROUND: The unicellular ancestors of modern-day multicellular organisms were remarkably complex. They had an extensive set of regulatory and signalling genes, an intricate life cycle and could change their behaviour in response to environmental changes. At the transition to multicellularity, some of these behaviours were co-opted to organise the development of the nascent multicellular organism. Here, we focus on the transition to multicellularity before the evolution of stable cell differentiation, to reveal how the emergence of clusters affects the evolution of cell behaviour. RESULTS: We construct a computational model of a population of cells that can evolve the regulation of their behavioural state - either division or migration - and study both a unicellular and a multicellular context. Cells compete for reproduction and for resources to survive in a seasonally changing environment. We find that the evolution of multicellularity strongly determines the co-evolution of cell behaviour, by altering the competition dynamics between cells. When adhesion cannot evolve, cells compete for survival by rapidly migrating towards resources before dividing. When adhesion evolves, emergent collective migration alleviates the pressure on individual cells to reach resources. This allows individual cells to maximise their own replication. Migrating adhesive clusters display striking patterns of spatio-temporal cell state changes that visually resemble animal development. CONCLUSIONS: Our model demonstrates how emergent selection pressures at the onset of multicellularity can drive the evolution of cellular behaviour to give rise to developmental patterns. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12862-023-02133-x. BioMed Central 2023-07-19 /pmc/articles/PMC10357660/ /pubmed/37468829 http://dx.doi.org/10.1186/s12862-023-02133-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Vroomans, Renske M. A.
Colizzi, Enrico Sandro
Evolution of selfish multicellularity: collective organisation of individual spatio-temporal regulatory strategies
title Evolution of selfish multicellularity: collective organisation of individual spatio-temporal regulatory strategies
title_full Evolution of selfish multicellularity: collective organisation of individual spatio-temporal regulatory strategies
title_fullStr Evolution of selfish multicellularity: collective organisation of individual spatio-temporal regulatory strategies
title_full_unstemmed Evolution of selfish multicellularity: collective organisation of individual spatio-temporal regulatory strategies
title_short Evolution of selfish multicellularity: collective organisation of individual spatio-temporal regulatory strategies
title_sort evolution of selfish multicellularity: collective organisation of individual spatio-temporal regulatory strategies
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357660/
https://www.ncbi.nlm.nih.gov/pubmed/37468829
http://dx.doi.org/10.1186/s12862-023-02133-x
work_keys_str_mv AT vroomansrenskema evolutionofselfishmulticellularitycollectiveorganisationofindividualspatiotemporalregulatorystrategies
AT colizzienricosandro evolutionofselfishmulticellularitycollectiveorganisationofindividualspatiotemporalregulatorystrategies