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A speciation gene for left–right reversal in snails results in anti-predator adaptation
How speciation genes can spread in a population is poorly understood. In land snails, a single gene for left–right reversal could be responsible for instant speciation, because dextral and sinistral snails have difficulty in mating. However, the traditional two-locus speciation model predicts that a...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105295/ https://www.ncbi.nlm.nih.gov/pubmed/21139578 http://dx.doi.org/10.1038/ncomms1133 |
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author | Hoso, Masaki Kameda, Yuichi Wu, Shu-Ping Asami, Takahiro Kato, Makoto Hori, Michio |
author_facet | Hoso, Masaki Kameda, Yuichi Wu, Shu-Ping Asami, Takahiro Kato, Makoto Hori, Michio |
author_sort | Hoso, Masaki |
collection | PubMed |
description | How speciation genes can spread in a population is poorly understood. In land snails, a single gene for left–right reversal could be responsible for instant speciation, because dextral and sinistral snails have difficulty in mating. However, the traditional two-locus speciation model predicts that a mating disadvantage for the reversal should counteract this speciation. In this study, we show that specialized snake predation of the dextral majority drives prey speciation by reversal. Our experiments demonstrate that sinistral Satsuma snails (Stylommatophora: Camaenidae) survive predation by Pareas iwasakii (Colubroidea: Pareatidae). Worldwide biogeography reveals that stylommatophoran snail speciation by reversal has been accelerated in the range of pareatid snakes, especially in snails that gain stronger anti-snake defense and reproductive isolation from dextrals by sinistrality. Molecular phylogeny of Satsuma snails further provides intriguing evidence of repetitive speciation under snake predation. Our study demonstrates that a speciation gene can be fixed in populations by positive pleiotropic effects on survival. |
format | Text |
id | pubmed-3105295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-31052952011-06-01 A speciation gene for left–right reversal in snails results in anti-predator adaptation Hoso, Masaki Kameda, Yuichi Wu, Shu-Ping Asami, Takahiro Kato, Makoto Hori, Michio Nat Commun Article How speciation genes can spread in a population is poorly understood. In land snails, a single gene for left–right reversal could be responsible for instant speciation, because dextral and sinistral snails have difficulty in mating. However, the traditional two-locus speciation model predicts that a mating disadvantage for the reversal should counteract this speciation. In this study, we show that specialized snake predation of the dextral majority drives prey speciation by reversal. Our experiments demonstrate that sinistral Satsuma snails (Stylommatophora: Camaenidae) survive predation by Pareas iwasakii (Colubroidea: Pareatidae). Worldwide biogeography reveals that stylommatophoran snail speciation by reversal has been accelerated in the range of pareatid snakes, especially in snails that gain stronger anti-snake defense and reproductive isolation from dextrals by sinistrality. Molecular phylogeny of Satsuma snails further provides intriguing evidence of repetitive speciation under snake predation. Our study demonstrates that a speciation gene can be fixed in populations by positive pleiotropic effects on survival. Nature Publishing Group 2010-12-07 /pmc/articles/PMC3105295/ /pubmed/21139578 http://dx.doi.org/10.1038/ncomms1133 Text en Copyright © 2010, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Article Hoso, Masaki Kameda, Yuichi Wu, Shu-Ping Asami, Takahiro Kato, Makoto Hori, Michio A speciation gene for left–right reversal in snails results in anti-predator adaptation |
title | A speciation gene for left–right reversal in snails results in anti-predator adaptation |
title_full | A speciation gene for left–right reversal in snails results in anti-predator adaptation |
title_fullStr | A speciation gene for left–right reversal in snails results in anti-predator adaptation |
title_full_unstemmed | A speciation gene for left–right reversal in snails results in anti-predator adaptation |
title_short | A speciation gene for left–right reversal in snails results in anti-predator adaptation |
title_sort | speciation gene for left–right reversal in snails results in anti-predator adaptation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105295/ https://www.ncbi.nlm.nih.gov/pubmed/21139578 http://dx.doi.org/10.1038/ncomms1133 |
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