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Multispecies interactions shape the transition to multicellularity

The origin of multicellularity transformed the adaptive landscape on Earth, opening diverse avenues for further innovation. The transition to multicellular life is understood as the evolution of cooperative groups which form a new level of individuality. Despite the potential for community-level int...

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Autores principales: Kalambokidis, Maria, Travisano, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509594/
https://www.ncbi.nlm.nih.gov/pubmed/37727086
http://dx.doi.org/10.1098/rspb.2023.1055
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author Kalambokidis, Maria
Travisano, Michael
author_facet Kalambokidis, Maria
Travisano, Michael
author_sort Kalambokidis, Maria
collection PubMed
description The origin of multicellularity transformed the adaptive landscape on Earth, opening diverse avenues for further innovation. The transition to multicellular life is understood as the evolution of cooperative groups which form a new level of individuality. Despite the potential for community-level interactions, most studies have not addressed the competitive context of this transition, such as competition between species. Here, we explore how interspecific competition shapes the emergence of multicellularity in an experimental system with two yeast species, Saccharomyces cerevisiae and Kluyveromyces lactis, where multicellularity evolves in response to selection for faster settling ability. We find that the multispecies context slows the rate of the transition to multicellularity, and the transition to multicellularity significantly impacts community composition. Multicellular K. lactis emerges first and sweeps through populations in monocultures faster than in cocultures with S. cerevisiae. Following the transition, the between-species competitive dynamics shift, likely in part to intraspecific cooperation in K. lactis. Hence, we document an eco-evolutionary feedback across the transition to multicellularity, underscoring how ecological context is critical for understanding the causes and consequences of innovation. By including two species, we demonstrate that cooperation and competition across several biological scales shapes the origin and persistence of multicellularity.
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spelling pubmed-105095942023-09-21 Multispecies interactions shape the transition to multicellularity Kalambokidis, Maria Travisano, Michael Proc Biol Sci Evolution The origin of multicellularity transformed the adaptive landscape on Earth, opening diverse avenues for further innovation. The transition to multicellular life is understood as the evolution of cooperative groups which form a new level of individuality. Despite the potential for community-level interactions, most studies have not addressed the competitive context of this transition, such as competition between species. Here, we explore how interspecific competition shapes the emergence of multicellularity in an experimental system with two yeast species, Saccharomyces cerevisiae and Kluyveromyces lactis, where multicellularity evolves in response to selection for faster settling ability. We find that the multispecies context slows the rate of the transition to multicellularity, and the transition to multicellularity significantly impacts community composition. Multicellular K. lactis emerges first and sweeps through populations in monocultures faster than in cocultures with S. cerevisiae. Following the transition, the between-species competitive dynamics shift, likely in part to intraspecific cooperation in K. lactis. Hence, we document an eco-evolutionary feedback across the transition to multicellularity, underscoring how ecological context is critical for understanding the causes and consequences of innovation. By including two species, we demonstrate that cooperation and competition across several biological scales shapes the origin and persistence of multicellularity. The Royal Society 2023-09-20 /pmc/articles/PMC10509594/ /pubmed/37727086 http://dx.doi.org/10.1098/rspb.2023.1055 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Kalambokidis, Maria
Travisano, Michael
Multispecies interactions shape the transition to multicellularity
title Multispecies interactions shape the transition to multicellularity
title_full Multispecies interactions shape the transition to multicellularity
title_fullStr Multispecies interactions shape the transition to multicellularity
title_full_unstemmed Multispecies interactions shape the transition to multicellularity
title_short Multispecies interactions shape the transition to multicellularity
title_sort multispecies interactions shape the transition to multicellularity
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509594/
https://www.ncbi.nlm.nih.gov/pubmed/37727086
http://dx.doi.org/10.1098/rspb.2023.1055
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