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Phenotypic effects of the Y chromosome are variable and structured in hybrids among house mouse recombinant lines
Hybrid zones between divergent populations sieve genomes into blocks that introgress across the zone, and blocks that do not, depending on selection between interacting genes. Consistent with Haldane's rule, the Y chromosome has been considered counterselected and hence not to introgress across...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540687/ https://www.ncbi.nlm.nih.gov/pubmed/31161024 http://dx.doi.org/10.1002/ece3.5196 |
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author | Martincová, Iva Ďureje, Ľudovít Kreisinger, Jakub Macholán, Miloš Piálek, Jaroslav |
author_facet | Martincová, Iva Ďureje, Ľudovít Kreisinger, Jakub Macholán, Miloš Piálek, Jaroslav |
author_sort | Martincová, Iva |
collection | PubMed |
description | Hybrid zones between divergent populations sieve genomes into blocks that introgress across the zone, and blocks that do not, depending on selection between interacting genes. Consistent with Haldane's rule, the Y chromosome has been considered counterselected and hence not to introgress across the European house mouse hybrid zone. However, recent studies detected massive invasion of M. m. musculus Y chromosomes into M. m. domesticus territory. To understand mechanisms facilitating Y spread, we created 31 recombinant lines from eight wild‐derived strains representing four localities within the two mouse subspecies. These lines were reciprocally crossed and resulting F1 hybrid males scored for five phenotypic traits associated with male fitness. Molecular analyses of 51 Y‐linked SNPs attributed ~50% of genetic variation to differences between the subspecies and 8% to differentiation within both taxa. A striking proportion, 21% (frequencies of sperm head abnormalities) and 42% (frequencies of sperm tail dissociations), of phenotypic variation was explained by geographic Y chromosome variants. Our crossing design allowed this explanatory power to be examined across a hierarchical scale from subspecific to local intrastrain effects. We found that divergence and variation were expressed diversely in different phenotypic traits and varied across the whole hierarchical scale. This finding adds another dimension of complexity to studies of Y introgression not only across the house mouse hybrid zone but potentially also in other contact zones. |
format | Online Article Text |
id | pubmed-6540687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65406872019-06-03 Phenotypic effects of the Y chromosome are variable and structured in hybrids among house mouse recombinant lines Martincová, Iva Ďureje, Ľudovít Kreisinger, Jakub Macholán, Miloš Piálek, Jaroslav Ecol Evol Original Research Hybrid zones between divergent populations sieve genomes into blocks that introgress across the zone, and blocks that do not, depending on selection between interacting genes. Consistent with Haldane's rule, the Y chromosome has been considered counterselected and hence not to introgress across the European house mouse hybrid zone. However, recent studies detected massive invasion of M. m. musculus Y chromosomes into M. m. domesticus territory. To understand mechanisms facilitating Y spread, we created 31 recombinant lines from eight wild‐derived strains representing four localities within the two mouse subspecies. These lines were reciprocally crossed and resulting F1 hybrid males scored for five phenotypic traits associated with male fitness. Molecular analyses of 51 Y‐linked SNPs attributed ~50% of genetic variation to differences between the subspecies and 8% to differentiation within both taxa. A striking proportion, 21% (frequencies of sperm head abnormalities) and 42% (frequencies of sperm tail dissociations), of phenotypic variation was explained by geographic Y chromosome variants. Our crossing design allowed this explanatory power to be examined across a hierarchical scale from subspecific to local intrastrain effects. We found that divergence and variation were expressed diversely in different phenotypic traits and varied across the whole hierarchical scale. This finding adds another dimension of complexity to studies of Y introgression not only across the house mouse hybrid zone but potentially also in other contact zones. John Wiley and Sons Inc. 2019-05-07 /pmc/articles/PMC6540687/ /pubmed/31161024 http://dx.doi.org/10.1002/ece3.5196 Text en © 2019 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Martincová, Iva Ďureje, Ľudovít Kreisinger, Jakub Macholán, Miloš Piálek, Jaroslav Phenotypic effects of the Y chromosome are variable and structured in hybrids among house mouse recombinant lines |
title | Phenotypic effects of the Y chromosome are variable and structured in hybrids among house mouse recombinant lines |
title_full | Phenotypic effects of the Y chromosome are variable and structured in hybrids among house mouse recombinant lines |
title_fullStr | Phenotypic effects of the Y chromosome are variable and structured in hybrids among house mouse recombinant lines |
title_full_unstemmed | Phenotypic effects of the Y chromosome are variable and structured in hybrids among house mouse recombinant lines |
title_short | Phenotypic effects of the Y chromosome are variable and structured in hybrids among house mouse recombinant lines |
title_sort | phenotypic effects of the y chromosome are variable and structured in hybrids among house mouse recombinant lines |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540687/ https://www.ncbi.nlm.nih.gov/pubmed/31161024 http://dx.doi.org/10.1002/ece3.5196 |
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