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Two transcriptionally distinct pathways drive female development in a reptile with both genetic and temperature dependent sex determination
How temperature determines sex remains unknown. A recent hypothesis proposes that conserved cellular mechanisms (calcium and redox; ‘CaRe’ status) sense temperature and identify genes and regulatory pathways likely to be involved in driving sexual development. We take advantage of the unique sex det...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049264/ https://www.ncbi.nlm.nih.gov/pubmed/33857129 http://dx.doi.org/10.1371/journal.pgen.1009465 |
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author | Whiteley, Sarah L. Holleley, Clare E. Wagner, Susan Blackburn, James Deveson, Ira W. Marshall Graves, Jennifer A. Georges, Arthur |
author_facet | Whiteley, Sarah L. Holleley, Clare E. Wagner, Susan Blackburn, James Deveson, Ira W. Marshall Graves, Jennifer A. Georges, Arthur |
author_sort | Whiteley, Sarah L. |
collection | PubMed |
description | How temperature determines sex remains unknown. A recent hypothesis proposes that conserved cellular mechanisms (calcium and redox; ‘CaRe’ status) sense temperature and identify genes and regulatory pathways likely to be involved in driving sexual development. We take advantage of the unique sex determining system of the model organism, Pogona vitticeps, to assess predictions of this hypothesis. P. vitticeps has ZZ male: ZW female sex chromosomes whose influence can be overridden in genetic males by high temperatures, causing male-to-female sex reversal. We compare a developmental transcriptome series of ZWf females and temperature sex reversed ZZf females. We demonstrate that early developmental cascades differ dramatically between genetically driven and thermally driven females, later converging to produce a common outcome (ovaries). We show that genes proposed as regulators of thermosensitive sex determination play a role in temperature sex reversal. Our study greatly advances the search for the mechanisms by which temperature determines sex. |
format | Online Article Text |
id | pubmed-8049264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-80492642021-04-21 Two transcriptionally distinct pathways drive female development in a reptile with both genetic and temperature dependent sex determination Whiteley, Sarah L. Holleley, Clare E. Wagner, Susan Blackburn, James Deveson, Ira W. Marshall Graves, Jennifer A. Georges, Arthur PLoS Genet Research Article How temperature determines sex remains unknown. A recent hypothesis proposes that conserved cellular mechanisms (calcium and redox; ‘CaRe’ status) sense temperature and identify genes and regulatory pathways likely to be involved in driving sexual development. We take advantage of the unique sex determining system of the model organism, Pogona vitticeps, to assess predictions of this hypothesis. P. vitticeps has ZZ male: ZW female sex chromosomes whose influence can be overridden in genetic males by high temperatures, causing male-to-female sex reversal. We compare a developmental transcriptome series of ZWf females and temperature sex reversed ZZf females. We demonstrate that early developmental cascades differ dramatically between genetically driven and thermally driven females, later converging to produce a common outcome (ovaries). We show that genes proposed as regulators of thermosensitive sex determination play a role in temperature sex reversal. Our study greatly advances the search for the mechanisms by which temperature determines sex. Public Library of Science 2021-04-15 /pmc/articles/PMC8049264/ /pubmed/33857129 http://dx.doi.org/10.1371/journal.pgen.1009465 Text en © 2021 Whiteley et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Whiteley, Sarah L. Holleley, Clare E. Wagner, Susan Blackburn, James Deveson, Ira W. Marshall Graves, Jennifer A. Georges, Arthur Two transcriptionally distinct pathways drive female development in a reptile with both genetic and temperature dependent sex determination |
title | Two transcriptionally distinct pathways drive female development in a reptile with both genetic and temperature dependent sex determination |
title_full | Two transcriptionally distinct pathways drive female development in a reptile with both genetic and temperature dependent sex determination |
title_fullStr | Two transcriptionally distinct pathways drive female development in a reptile with both genetic and temperature dependent sex determination |
title_full_unstemmed | Two transcriptionally distinct pathways drive female development in a reptile with both genetic and temperature dependent sex determination |
title_short | Two transcriptionally distinct pathways drive female development in a reptile with both genetic and temperature dependent sex determination |
title_sort | two transcriptionally distinct pathways drive female development in a reptile with both genetic and temperature dependent sex determination |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049264/ https://www.ncbi.nlm.nih.gov/pubmed/33857129 http://dx.doi.org/10.1371/journal.pgen.1009465 |
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