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Neuropeptide signalling shapes feeding and reproductive behaviours in male Caenorhabditis elegans
Sexual dimorphism occurs where different sexes of the same species display differences in characteristics not limited to reproduction. For the nematode Caenorhabditis elegans, in which the complete neuroanatomy has been solved for both hermaphrodites and males, sexually dimorphic features have been...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233197/ https://www.ncbi.nlm.nih.gov/pubmed/35738805 http://dx.doi.org/10.26508/lsa.202201420 |
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author | Gadenne, Matthew J Hardege, Iris Yemini, Eviatar Suleski, Djordji Jaggers, Paris Beets, Isabel Schafer, William R Chew, Yee Lian |
author_facet | Gadenne, Matthew J Hardege, Iris Yemini, Eviatar Suleski, Djordji Jaggers, Paris Beets, Isabel Schafer, William R Chew, Yee Lian |
author_sort | Gadenne, Matthew J |
collection | PubMed |
description | Sexual dimorphism occurs where different sexes of the same species display differences in characteristics not limited to reproduction. For the nematode Caenorhabditis elegans, in which the complete neuroanatomy has been solved for both hermaphrodites and males, sexually dimorphic features have been observed both in terms of the number of neurons and in synaptic connectivity. In addition, male behaviours, such as food-leaving to prioritise searching for mates, have been attributed to neuropeptides released from sex-shared or sex-specific neurons. In this study, we show that the lury-1 neuropeptide gene shows a sexually dimorphic expression pattern; being expressed in pharyngeal neurons in both sexes but displaying additional expression in tail neurons only in the male. We also show that lury-1 mutant animals show sex differences in feeding behaviours, with pharyngeal pumping elevated in hermaphrodites but reduced in males. LURY-1 also modulates male mating efficiency, influencing motor events during contact with a hermaphrodite. Our findings indicate sex-specific roles of this peptide in feeding and reproduction in C. elegans, providing further insight into neuromodulatory control of sexually dimorphic behaviours. |
format | Online Article Text |
id | pubmed-9233197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-92331972022-07-13 Neuropeptide signalling shapes feeding and reproductive behaviours in male Caenorhabditis elegans Gadenne, Matthew J Hardege, Iris Yemini, Eviatar Suleski, Djordji Jaggers, Paris Beets, Isabel Schafer, William R Chew, Yee Lian Life Sci Alliance Research Articles Sexual dimorphism occurs where different sexes of the same species display differences in characteristics not limited to reproduction. For the nematode Caenorhabditis elegans, in which the complete neuroanatomy has been solved for both hermaphrodites and males, sexually dimorphic features have been observed both in terms of the number of neurons and in synaptic connectivity. In addition, male behaviours, such as food-leaving to prioritise searching for mates, have been attributed to neuropeptides released from sex-shared or sex-specific neurons. In this study, we show that the lury-1 neuropeptide gene shows a sexually dimorphic expression pattern; being expressed in pharyngeal neurons in both sexes but displaying additional expression in tail neurons only in the male. We also show that lury-1 mutant animals show sex differences in feeding behaviours, with pharyngeal pumping elevated in hermaphrodites but reduced in males. LURY-1 also modulates male mating efficiency, influencing motor events during contact with a hermaphrodite. Our findings indicate sex-specific roles of this peptide in feeding and reproduction in C. elegans, providing further insight into neuromodulatory control of sexually dimorphic behaviours. Life Science Alliance LLC 2022-06-23 /pmc/articles/PMC9233197/ /pubmed/35738805 http://dx.doi.org/10.26508/lsa.202201420 Text en © 2022 Gadenne et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Articles Gadenne, Matthew J Hardege, Iris Yemini, Eviatar Suleski, Djordji Jaggers, Paris Beets, Isabel Schafer, William R Chew, Yee Lian Neuropeptide signalling shapes feeding and reproductive behaviours in male Caenorhabditis elegans |
title | Neuropeptide signalling shapes feeding and reproductive behaviours in male Caenorhabditis elegans |
title_full | Neuropeptide signalling shapes feeding and reproductive behaviours in male Caenorhabditis elegans |
title_fullStr | Neuropeptide signalling shapes feeding and reproductive behaviours in male Caenorhabditis elegans |
title_full_unstemmed | Neuropeptide signalling shapes feeding and reproductive behaviours in male Caenorhabditis elegans |
title_short | Neuropeptide signalling shapes feeding and reproductive behaviours in male Caenorhabditis elegans |
title_sort | neuropeptide signalling shapes feeding and reproductive behaviours in male caenorhabditis elegans |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233197/ https://www.ncbi.nlm.nih.gov/pubmed/35738805 http://dx.doi.org/10.26508/lsa.202201420 |
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