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The genetic basis of natural variation in a phoretic behavior

Phoresy is a widespread form of commensalism that facilitates dispersal of one species through an association with a more mobile second species. Dauer larvae of the nematode Caenorhabditis elegans exhibit a phoretic behavior called nictation, which could enable interactions with animals such as isop...

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Autores principales: Lee, Daehan, Yang, Heeseung, Kim, Jun, Brady, Shannon, Zdraljevic, Stefan, Zamanian, Mostafa, Kim, Heekyeong, Paik, Young-ki, Kruglyak, Leonid, Andersen, Erik C., Lee, Junho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561207/
https://www.ncbi.nlm.nih.gov/pubmed/28819099
http://dx.doi.org/10.1038/s41467-017-00386-x
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author Lee, Daehan
Yang, Heeseung
Kim, Jun
Brady, Shannon
Zdraljevic, Stefan
Zamanian, Mostafa
Kim, Heekyeong
Paik, Young-ki
Kruglyak, Leonid
Andersen, Erik C.
Lee, Junho
author_facet Lee, Daehan
Yang, Heeseung
Kim, Jun
Brady, Shannon
Zdraljevic, Stefan
Zamanian, Mostafa
Kim, Heekyeong
Paik, Young-ki
Kruglyak, Leonid
Andersen, Erik C.
Lee, Junho
author_sort Lee, Daehan
collection PubMed
description Phoresy is a widespread form of commensalism that facilitates dispersal of one species through an association with a more mobile second species. Dauer larvae of the nematode Caenorhabditis elegans exhibit a phoretic behavior called nictation, which could enable interactions with animals such as isopods or snails. Here, we show that natural C. elegans isolates differ in nictation. We use quantitative behavioral assays and linkage mapping to identify a genetic locus (nict-1) that mediates the phoretic interaction with terrestrial isopods. The nict-1 locus contains a Piwi-interacting small RNA (piRNA) cluster; we observe that the Piwi Argonaute PRG-1 is involved in the regulation of nictation. Additionally, this locus underlies a trade-off between offspring production and dispersal. Variation in the nict-1 locus contributes directly to differences in association between nematodes and terrestrial isopods in a laboratory assay. In summary, the piRNA-rich nict-1 locus could define a novel mechanism underlying phoretic interactions.
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spelling pubmed-55612072017-08-28 The genetic basis of natural variation in a phoretic behavior Lee, Daehan Yang, Heeseung Kim, Jun Brady, Shannon Zdraljevic, Stefan Zamanian, Mostafa Kim, Heekyeong Paik, Young-ki Kruglyak, Leonid Andersen, Erik C. Lee, Junho Nat Commun Article Phoresy is a widespread form of commensalism that facilitates dispersal of one species through an association with a more mobile second species. Dauer larvae of the nematode Caenorhabditis elegans exhibit a phoretic behavior called nictation, which could enable interactions with animals such as isopods or snails. Here, we show that natural C. elegans isolates differ in nictation. We use quantitative behavioral assays and linkage mapping to identify a genetic locus (nict-1) that mediates the phoretic interaction with terrestrial isopods. The nict-1 locus contains a Piwi-interacting small RNA (piRNA) cluster; we observe that the Piwi Argonaute PRG-1 is involved in the regulation of nictation. Additionally, this locus underlies a trade-off between offspring production and dispersal. Variation in the nict-1 locus contributes directly to differences in association between nematodes and terrestrial isopods in a laboratory assay. In summary, the piRNA-rich nict-1 locus could define a novel mechanism underlying phoretic interactions. Nature Publishing Group UK 2017-08-17 /pmc/articles/PMC5561207/ /pubmed/28819099 http://dx.doi.org/10.1038/s41467-017-00386-x Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lee, Daehan
Yang, Heeseung
Kim, Jun
Brady, Shannon
Zdraljevic, Stefan
Zamanian, Mostafa
Kim, Heekyeong
Paik, Young-ki
Kruglyak, Leonid
Andersen, Erik C.
Lee, Junho
The genetic basis of natural variation in a phoretic behavior
title The genetic basis of natural variation in a phoretic behavior
title_full The genetic basis of natural variation in a phoretic behavior
title_fullStr The genetic basis of natural variation in a phoretic behavior
title_full_unstemmed The genetic basis of natural variation in a phoretic behavior
title_short The genetic basis of natural variation in a phoretic behavior
title_sort genetic basis of natural variation in a phoretic behavior
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561207/
https://www.ncbi.nlm.nih.gov/pubmed/28819099
http://dx.doi.org/10.1038/s41467-017-00386-x
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