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Cell–cell signalling in sexual chemotaxis: a basis for gametic differentiation, mating types and sexes

While sex requires two parents, there is no obvious need for them to be differentiated into distinct mating types or sexes. Yet this is the predominate state of nature. Here, we argue that mating types could play a decisive role because they prevent the apparent inevitability of self-stimulation dur...

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Detalles Bibliográficos
Autores principales: Hadjivasiliou, Zena, Iwasa, Yoh, Pomiankowski, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535405/
https://www.ncbi.nlm.nih.gov/pubmed/26156301
http://dx.doi.org/10.1098/rsif.2015.0342
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author Hadjivasiliou, Zena
Iwasa, Yoh
Pomiankowski, Andrew
author_facet Hadjivasiliou, Zena
Iwasa, Yoh
Pomiankowski, Andrew
author_sort Hadjivasiliou, Zena
collection PubMed
description While sex requires two parents, there is no obvious need for them to be differentiated into distinct mating types or sexes. Yet this is the predominate state of nature. Here, we argue that mating types could play a decisive role because they prevent the apparent inevitability of self-stimulation during sexual signalling. We rigorously assess this hypothesis by developing a model for signaller–detector dynamics based on chemical diffusion, chemotaxis and cell movement. Our model examines the conditions under which chemotaxis improves partner finding. Varying parameter values within ranges typical of protists and their environments, we show that simultaneous secretion and detection of a single chemoattractant can cause a multifold movement impediment and severely hinder mate finding. Mutually exclusive roles result in faster pair formation, even when cells conferring the same roles cannot pair up. This arrangement also allows the separate mating types to optimize their signalling or detecting roles, which is effectively impossible for cells that are both secretors and detectors. Our findings suggest that asymmetric roles in sexual chemotaxis (and possibly other forms of sexual signalling) are crucial, even without morphological differences, and may underlie the evolution of gametic differentiation among both mating types and sexes.
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spelling pubmed-45354052015-08-21 Cell–cell signalling in sexual chemotaxis: a basis for gametic differentiation, mating types and sexes Hadjivasiliou, Zena Iwasa, Yoh Pomiankowski, Andrew J R Soc Interface Research Articles While sex requires two parents, there is no obvious need for them to be differentiated into distinct mating types or sexes. Yet this is the predominate state of nature. Here, we argue that mating types could play a decisive role because they prevent the apparent inevitability of self-stimulation during sexual signalling. We rigorously assess this hypothesis by developing a model for signaller–detector dynamics based on chemical diffusion, chemotaxis and cell movement. Our model examines the conditions under which chemotaxis improves partner finding. Varying parameter values within ranges typical of protists and their environments, we show that simultaneous secretion and detection of a single chemoattractant can cause a multifold movement impediment and severely hinder mate finding. Mutually exclusive roles result in faster pair formation, even when cells conferring the same roles cannot pair up. This arrangement also allows the separate mating types to optimize their signalling or detecting roles, which is effectively impossible for cells that are both secretors and detectors. Our findings suggest that asymmetric roles in sexual chemotaxis (and possibly other forms of sexual signalling) are crucial, even without morphological differences, and may underlie the evolution of gametic differentiation among both mating types and sexes. The Royal Society 2015-08-06 /pmc/articles/PMC4535405/ /pubmed/26156301 http://dx.doi.org/10.1098/rsif.2015.0342 Text en © 2015 The Authors. http://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/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research Articles
Hadjivasiliou, Zena
Iwasa, Yoh
Pomiankowski, Andrew
Cell–cell signalling in sexual chemotaxis: a basis for gametic differentiation, mating types and sexes
title Cell–cell signalling in sexual chemotaxis: a basis for gametic differentiation, mating types and sexes
title_full Cell–cell signalling in sexual chemotaxis: a basis for gametic differentiation, mating types and sexes
title_fullStr Cell–cell signalling in sexual chemotaxis: a basis for gametic differentiation, mating types and sexes
title_full_unstemmed Cell–cell signalling in sexual chemotaxis: a basis for gametic differentiation, mating types and sexes
title_short Cell–cell signalling in sexual chemotaxis: a basis for gametic differentiation, mating types and sexes
title_sort cell–cell signalling in sexual chemotaxis: a basis for gametic differentiation, mating types and sexes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535405/
https://www.ncbi.nlm.nih.gov/pubmed/26156301
http://dx.doi.org/10.1098/rsif.2015.0342
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