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Sex reversal explains some, but not all, climate-mediated sex ratio variation within a viviparous reptile
Evolutionary transitions in sex-determining systems have occurred frequently yet understanding how they occur remains a major challenge. In reptiles, transitions from genetic to temperature-dependent sex determination can occur if the gene products that determine sex evolve thermal sensitivity, resu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156933/ https://www.ncbi.nlm.nih.gov/pubmed/35642367 http://dx.doi.org/10.1098/rspb.2022.0689 |
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author | Hill, Peta While, Geoffrey M. Burridge, Christopher P. Ezaz, Tariq Munch, Kirke L. McVarish, Mary Wapstra, Erik |
author_facet | Hill, Peta While, Geoffrey M. Burridge, Christopher P. Ezaz, Tariq Munch, Kirke L. McVarish, Mary Wapstra, Erik |
author_sort | Hill, Peta |
collection | PubMed |
description | Evolutionary transitions in sex-determining systems have occurred frequently yet understanding how they occur remains a major challenge. In reptiles, transitions from genetic to temperature-dependent sex determination can occur if the gene products that determine sex evolve thermal sensitivity, resulting in sex-reversed individuals. However, evidence of sex reversal is limited to oviparous reptiles. Here we used thermal experiments to test whether sex reversal is responsible for differences in sex determination in a viviparous reptile, Carinascincus ocellatus, a species with XY sex chromosomes and population-specific sex ratio response to temperature. We show that sex reversal is occurring and that its frequency is related to temperature. Sex reversal was unidirectional (phenotypic males with XX genotype) and observed in both high- and low-elevation populations. We propose that XX-biased genotypic sex ratios could produce either male- or female-biased phenotypic sex ratios as observed in low-elevation C. ocellatus under variable rates of XX sex reversal. We discuss reasons why sex reversal may not influence sex ratios at high elevation. Our results suggest that the mechanism responsible for evolutionary transitions from genotypic to temperature-dependent sex determination is more complex than can be explained by a single process such as sex reversal. |
format | Online Article Text |
id | pubmed-9156933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-91569332022-06-13 Sex reversal explains some, but not all, climate-mediated sex ratio variation within a viviparous reptile Hill, Peta While, Geoffrey M. Burridge, Christopher P. Ezaz, Tariq Munch, Kirke L. McVarish, Mary Wapstra, Erik Proc Biol Sci Genetics and Genomics Evolutionary transitions in sex-determining systems have occurred frequently yet understanding how they occur remains a major challenge. In reptiles, transitions from genetic to temperature-dependent sex determination can occur if the gene products that determine sex evolve thermal sensitivity, resulting in sex-reversed individuals. However, evidence of sex reversal is limited to oviparous reptiles. Here we used thermal experiments to test whether sex reversal is responsible for differences in sex determination in a viviparous reptile, Carinascincus ocellatus, a species with XY sex chromosomes and population-specific sex ratio response to temperature. We show that sex reversal is occurring and that its frequency is related to temperature. Sex reversal was unidirectional (phenotypic males with XX genotype) and observed in both high- and low-elevation populations. We propose that XX-biased genotypic sex ratios could produce either male- or female-biased phenotypic sex ratios as observed in low-elevation C. ocellatus under variable rates of XX sex reversal. We discuss reasons why sex reversal may not influence sex ratios at high elevation. Our results suggest that the mechanism responsible for evolutionary transitions from genotypic to temperature-dependent sex determination is more complex than can be explained by a single process such as sex reversal. The Royal Society 2022-06-08 2022-06-01 /pmc/articles/PMC9156933/ /pubmed/35642367 http://dx.doi.org/10.1098/rspb.2022.0689 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Genetics and Genomics Hill, Peta While, Geoffrey M. Burridge, Christopher P. Ezaz, Tariq Munch, Kirke L. McVarish, Mary Wapstra, Erik Sex reversal explains some, but not all, climate-mediated sex ratio variation within a viviparous reptile |
title | Sex reversal explains some, but not all, climate-mediated sex ratio variation within a viviparous reptile |
title_full | Sex reversal explains some, but not all, climate-mediated sex ratio variation within a viviparous reptile |
title_fullStr | Sex reversal explains some, but not all, climate-mediated sex ratio variation within a viviparous reptile |
title_full_unstemmed | Sex reversal explains some, but not all, climate-mediated sex ratio variation within a viviparous reptile |
title_short | Sex reversal explains some, but not all, climate-mediated sex ratio variation within a viviparous reptile |
title_sort | sex reversal explains some, but not all, climate-mediated sex ratio variation within a viviparous reptile |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156933/ https://www.ncbi.nlm.nih.gov/pubmed/35642367 http://dx.doi.org/10.1098/rspb.2022.0689 |
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