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Direct glia-to-neuron transdifferentiation gives rise to a pair of male-specific neurons that ensure nimble male mating

Sexually dimorphic behaviours require underlying differences in the nervous system between males and females. The extent to which nervous systems are sexually dimorphic and the cellular and molecular mechanisms that regulate these differences are only beginning to be understood. We reveal here a nov...

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Autores principales: Molina-García, Laura, Lloret-Fernández, Carla, Cook, Steven J, Kim, Byunghyuk, Bonnington, Rachel C, Sammut, Michele, O'Shea, Jack M, Gilbert, Sophie PR, Elliott, David J, Hall, David H, Emmons, Scott W, Barrios, Arantza, Poole, Richard J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7609048/
https://www.ncbi.nlm.nih.gov/pubmed/33138916
http://dx.doi.org/10.7554/eLife.48361
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author Molina-García, Laura
Lloret-Fernández, Carla
Cook, Steven J
Kim, Byunghyuk
Bonnington, Rachel C
Sammut, Michele
O'Shea, Jack M
Gilbert, Sophie PR
Elliott, David J
Hall, David H
Emmons, Scott W
Barrios, Arantza
Poole, Richard J
author_facet Molina-García, Laura
Lloret-Fernández, Carla
Cook, Steven J
Kim, Byunghyuk
Bonnington, Rachel C
Sammut, Michele
O'Shea, Jack M
Gilbert, Sophie PR
Elliott, David J
Hall, David H
Emmons, Scott W
Barrios, Arantza
Poole, Richard J
author_sort Molina-García, Laura
collection PubMed
description Sexually dimorphic behaviours require underlying differences in the nervous system between males and females. The extent to which nervous systems are sexually dimorphic and the cellular and molecular mechanisms that regulate these differences are only beginning to be understood. We reveal here a novel mechanism by which male-specific neurons are generated in Caenorhabditis elegans through the direct transdifferentiation of sex-shared glial cells. This glia-to-neuron cell fate switch occurs during male sexual maturation under the cell-autonomous control of the sex-determination pathway. We show that the neurons generated are cholinergic, peptidergic, and ciliated putative proprioceptors which integrate into male-specific circuits for copulation. These neurons ensure coordinated backward movement along the mate’s body during mating. One step of the mating sequence regulated by these neurons is an alternative readjustment movement performed when intromission becomes difficult to achieve. Our findings reveal programmed transdifferentiation as a developmental mechanism underlying flexibility in innate behaviour.
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spelling pubmed-76090482020-11-04 Direct glia-to-neuron transdifferentiation gives rise to a pair of male-specific neurons that ensure nimble male mating Molina-García, Laura Lloret-Fernández, Carla Cook, Steven J Kim, Byunghyuk Bonnington, Rachel C Sammut, Michele O'Shea, Jack M Gilbert, Sophie PR Elliott, David J Hall, David H Emmons, Scott W Barrios, Arantza Poole, Richard J eLife Developmental Biology Sexually dimorphic behaviours require underlying differences in the nervous system between males and females. The extent to which nervous systems are sexually dimorphic and the cellular and molecular mechanisms that regulate these differences are only beginning to be understood. We reveal here a novel mechanism by which male-specific neurons are generated in Caenorhabditis elegans through the direct transdifferentiation of sex-shared glial cells. This glia-to-neuron cell fate switch occurs during male sexual maturation under the cell-autonomous control of the sex-determination pathway. We show that the neurons generated are cholinergic, peptidergic, and ciliated putative proprioceptors which integrate into male-specific circuits for copulation. These neurons ensure coordinated backward movement along the mate’s body during mating. One step of the mating sequence regulated by these neurons is an alternative readjustment movement performed when intromission becomes difficult to achieve. Our findings reveal programmed transdifferentiation as a developmental mechanism underlying flexibility in innate behaviour. eLife Sciences Publications, Ltd 2020-11-03 /pmc/articles/PMC7609048/ /pubmed/33138916 http://dx.doi.org/10.7554/eLife.48361 Text en © 2020, Molina-García et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Molina-García, Laura
Lloret-Fernández, Carla
Cook, Steven J
Kim, Byunghyuk
Bonnington, Rachel C
Sammut, Michele
O'Shea, Jack M
Gilbert, Sophie PR
Elliott, David J
Hall, David H
Emmons, Scott W
Barrios, Arantza
Poole, Richard J
Direct glia-to-neuron transdifferentiation gives rise to a pair of male-specific neurons that ensure nimble male mating
title Direct glia-to-neuron transdifferentiation gives rise to a pair of male-specific neurons that ensure nimble male mating
title_full Direct glia-to-neuron transdifferentiation gives rise to a pair of male-specific neurons that ensure nimble male mating
title_fullStr Direct glia-to-neuron transdifferentiation gives rise to a pair of male-specific neurons that ensure nimble male mating
title_full_unstemmed Direct glia-to-neuron transdifferentiation gives rise to a pair of male-specific neurons that ensure nimble male mating
title_short Direct glia-to-neuron transdifferentiation gives rise to a pair of male-specific neurons that ensure nimble male mating
title_sort direct glia-to-neuron transdifferentiation gives rise to a pair of male-specific neurons that ensure nimble male mating
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7609048/
https://www.ncbi.nlm.nih.gov/pubmed/33138916
http://dx.doi.org/10.7554/eLife.48361
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