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Genetic Contributions to Ectopic Sperm Cell Migration in Caenorhabditis Nematodes
Reproductive barriers involving gametic incompatibilities can act to enhance population divergence and promote the persistence of species boundaries. Observing gametic interactions in internal fertilizing organisms, however, presents a considerable practical challenge to characterizing mechanisms of...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288822/ https://www.ncbi.nlm.nih.gov/pubmed/30327379 http://dx.doi.org/10.1534/g3.118.200785 |
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author | Ting, Janice J. Tsai, Caressa N. Schalkowski, Rebecca Cutter, Asher D. |
author_facet | Ting, Janice J. Tsai, Caressa N. Schalkowski, Rebecca Cutter, Asher D. |
author_sort | Ting, Janice J. |
collection | PubMed |
description | Reproductive barriers involving gametic incompatibilities can act to enhance population divergence and promote the persistence of species boundaries. Observing gametic interactions in internal fertilizing organisms, however, presents a considerable practical challenge to characterizing mechanisms of such gametic isolation. Here we exploit the transparency of Caenorhabditis nematodes to investigate gametic isolation mediated by sperm that can migrate to ectopic locations, with this sperm invasion capable of inducing female sterility and premature death. As a step toward identifying genetic factors and mechanisms associated with female susceptibility to sperm invasion, we characterized a panel of 25 C. elegans genetic mutants to test for effects on the incidence and severity of sperm invasion in both conspecific and inter-species matings. We found genetic perturbations to contribute to distinct patterns of susceptibility that identify ovulation dynamics and sperm guidance cues as modulators of ectopic sperm migration incidence and severity. Genotypes confer distinctive phenotypic sensitivities to the sperm from conspecific C. elegans males vs. heterospecific C. nigoni males, implicating evolution of functional divergence in the history of these species for components of sperm-reproductive tract interactions. Sexually-antagonistic co-evolution within species that drives divergent trait and molecular evolution between species provides a working model to explain mismatched species-specific gametic interactions that promote or mitigate ectopic sperm migration. |
format | Online Article Text |
id | pubmed-6288822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-62888222018-12-19 Genetic Contributions to Ectopic Sperm Cell Migration in Caenorhabditis Nematodes Ting, Janice J. Tsai, Caressa N. Schalkowski, Rebecca Cutter, Asher D. G3 (Bethesda) Investigations Reproductive barriers involving gametic incompatibilities can act to enhance population divergence and promote the persistence of species boundaries. Observing gametic interactions in internal fertilizing organisms, however, presents a considerable practical challenge to characterizing mechanisms of such gametic isolation. Here we exploit the transparency of Caenorhabditis nematodes to investigate gametic isolation mediated by sperm that can migrate to ectopic locations, with this sperm invasion capable of inducing female sterility and premature death. As a step toward identifying genetic factors and mechanisms associated with female susceptibility to sperm invasion, we characterized a panel of 25 C. elegans genetic mutants to test for effects on the incidence and severity of sperm invasion in both conspecific and inter-species matings. We found genetic perturbations to contribute to distinct patterns of susceptibility that identify ovulation dynamics and sperm guidance cues as modulators of ectopic sperm migration incidence and severity. Genotypes confer distinctive phenotypic sensitivities to the sperm from conspecific C. elegans males vs. heterospecific C. nigoni males, implicating evolution of functional divergence in the history of these species for components of sperm-reproductive tract interactions. Sexually-antagonistic co-evolution within species that drives divergent trait and molecular evolution between species provides a working model to explain mismatched species-specific gametic interactions that promote or mitigate ectopic sperm migration. Genetics Society of America 2018-10-16 /pmc/articles/PMC6288822/ /pubmed/30327379 http://dx.doi.org/10.1534/g3.118.200785 Text en Copyright © 2018 Ting et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigations Ting, Janice J. Tsai, Caressa N. Schalkowski, Rebecca Cutter, Asher D. Genetic Contributions to Ectopic Sperm Cell Migration in Caenorhabditis Nematodes |
title | Genetic Contributions to Ectopic Sperm Cell Migration in Caenorhabditis Nematodes |
title_full | Genetic Contributions to Ectopic Sperm Cell Migration in Caenorhabditis Nematodes |
title_fullStr | Genetic Contributions to Ectopic Sperm Cell Migration in Caenorhabditis Nematodes |
title_full_unstemmed | Genetic Contributions to Ectopic Sperm Cell Migration in Caenorhabditis Nematodes |
title_short | Genetic Contributions to Ectopic Sperm Cell Migration in Caenorhabditis Nematodes |
title_sort | genetic contributions to ectopic sperm cell migration in caenorhabditis nematodes |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288822/ https://www.ncbi.nlm.nih.gov/pubmed/30327379 http://dx.doi.org/10.1534/g3.118.200785 |
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