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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...

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Autores principales: Hill, Peta, While, Geoffrey M., Burridge, Christopher P., Ezaz, Tariq, Munch, Kirke L., McVarish, Mary, Wapstra, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
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.
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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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