Cargando…
Gene expression of male pathway genes sox9 and amh during early sex differentiation in a reptile departs from the classical amniote model
BACKGROUND: Sex determination is the process whereby the bipotential embryonic gonads become committed to differentiate into testes or ovaries. In genetic sex determination (GSD), the sex determining trigger is encoded by a gene on the sex chromosomes, which activates a network of downstream genes;...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163765/ https://www.ncbi.nlm.nih.gov/pubmed/37147622 http://dx.doi.org/10.1186/s12864-023-09334-0 |
_version_ | 1785037951783141376 |
---|---|
author | Wagner, Susan Whiteley, Sarah L. Castelli, Meghan Patel, Hardip R. Deveson, Ira W. Blackburn, James Holleley, Clare E. Marshall Graves, Jennifer A. Georges, Arthur |
author_facet | Wagner, Susan Whiteley, Sarah L. Castelli, Meghan Patel, Hardip R. Deveson, Ira W. Blackburn, James Holleley, Clare E. Marshall Graves, Jennifer A. Georges, Arthur |
author_sort | Wagner, Susan |
collection | PubMed |
description | BACKGROUND: Sex determination is the process whereby the bipotential embryonic gonads become committed to differentiate into testes or ovaries. In genetic sex determination (GSD), the sex determining trigger is encoded by a gene on the sex chromosomes, which activates a network of downstream genes; in mammals these include SOX9, AMH and DMRT1 in the male pathway, and FOXL2 in the female pathway. Although mammalian and avian GSD systems have been well studied, few data are available for reptilian GSD systems. RESULTS: We conducted an unbiased transcriptome-wide analysis of gonad development throughout differentiation in central bearded dragon (Pogona vitticeps) embryos with GSD. We found that sex differentiation of transcriptomic profiles occurs at a very early stage, before the gonad consolidates as a body distinct from the gonad-kidney complex. The male pathway genes dmrt1 and amh and the female pathway gene foxl2 play a key role in early sex differentiation in P. vitticeps, but the central player of the mammalian male trajectory, sox9, is not differentially expressed in P. vitticeps at the bipotential stage. The most striking difference from GSD systems of other amniotes is the high expression of the male pathway genes amh and sox9 in female gonads during development. We propose that a default male trajectory progresses if not repressed by a W-linked dominant gene that tips the balance of gene expression towards the female trajectory. Further, weighted gene expression correlation network analysis revealed novel candidates for male and female sex differentiation. CONCLUSION: Our data reveal that interpretation of putative mechanisms of GSD in reptiles cannot solely depend on lessons drawn from mammals. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09334-0. |
format | Online Article Text |
id | pubmed-10163765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101637652023-05-07 Gene expression of male pathway genes sox9 and amh during early sex differentiation in a reptile departs from the classical amniote model Wagner, Susan Whiteley, Sarah L. Castelli, Meghan Patel, Hardip R. Deveson, Ira W. Blackburn, James Holleley, Clare E. Marshall Graves, Jennifer A. Georges, Arthur BMC Genomics Research BACKGROUND: Sex determination is the process whereby the bipotential embryonic gonads become committed to differentiate into testes or ovaries. In genetic sex determination (GSD), the sex determining trigger is encoded by a gene on the sex chromosomes, which activates a network of downstream genes; in mammals these include SOX9, AMH and DMRT1 in the male pathway, and FOXL2 in the female pathway. Although mammalian and avian GSD systems have been well studied, few data are available for reptilian GSD systems. RESULTS: We conducted an unbiased transcriptome-wide analysis of gonad development throughout differentiation in central bearded dragon (Pogona vitticeps) embryos with GSD. We found that sex differentiation of transcriptomic profiles occurs at a very early stage, before the gonad consolidates as a body distinct from the gonad-kidney complex. The male pathway genes dmrt1 and amh and the female pathway gene foxl2 play a key role in early sex differentiation in P. vitticeps, but the central player of the mammalian male trajectory, sox9, is not differentially expressed in P. vitticeps at the bipotential stage. The most striking difference from GSD systems of other amniotes is the high expression of the male pathway genes amh and sox9 in female gonads during development. We propose that a default male trajectory progresses if not repressed by a W-linked dominant gene that tips the balance of gene expression towards the female trajectory. Further, weighted gene expression correlation network analysis revealed novel candidates for male and female sex differentiation. CONCLUSION: Our data reveal that interpretation of putative mechanisms of GSD in reptiles cannot solely depend on lessons drawn from mammals. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09334-0. BioMed Central 2023-05-05 /pmc/articles/PMC10163765/ /pubmed/37147622 http://dx.doi.org/10.1186/s12864-023-09334-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Wagner, Susan Whiteley, Sarah L. Castelli, Meghan Patel, Hardip R. Deveson, Ira W. Blackburn, James Holleley, Clare E. Marshall Graves, Jennifer A. Georges, Arthur Gene expression of male pathway genes sox9 and amh during early sex differentiation in a reptile departs from the classical amniote model |
title | Gene expression of male pathway genes sox9 and amh during early sex differentiation in a reptile departs from the classical amniote model |
title_full | Gene expression of male pathway genes sox9 and amh during early sex differentiation in a reptile departs from the classical amniote model |
title_fullStr | Gene expression of male pathway genes sox9 and amh during early sex differentiation in a reptile departs from the classical amniote model |
title_full_unstemmed | Gene expression of male pathway genes sox9 and amh during early sex differentiation in a reptile departs from the classical amniote model |
title_short | Gene expression of male pathway genes sox9 and amh during early sex differentiation in a reptile departs from the classical amniote model |
title_sort | gene expression of male pathway genes sox9 and amh during early sex differentiation in a reptile departs from the classical amniote model |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163765/ https://www.ncbi.nlm.nih.gov/pubmed/37147622 http://dx.doi.org/10.1186/s12864-023-09334-0 |
work_keys_str_mv | AT wagnersusan geneexpressionofmalepathwaygenessox9andamhduringearlysexdifferentiationinareptiledepartsfromtheclassicalamniotemodel AT whiteleysarahl geneexpressionofmalepathwaygenessox9andamhduringearlysexdifferentiationinareptiledepartsfromtheclassicalamniotemodel AT castellimeghan geneexpressionofmalepathwaygenessox9andamhduringearlysexdifferentiationinareptiledepartsfromtheclassicalamniotemodel AT patelhardipr geneexpressionofmalepathwaygenessox9andamhduringearlysexdifferentiationinareptiledepartsfromtheclassicalamniotemodel AT devesoniraw geneexpressionofmalepathwaygenessox9andamhduringearlysexdifferentiationinareptiledepartsfromtheclassicalamniotemodel AT blackburnjames geneexpressionofmalepathwaygenessox9andamhduringearlysexdifferentiationinareptiledepartsfromtheclassicalamniotemodel AT holleleyclaree geneexpressionofmalepathwaygenessox9andamhduringearlysexdifferentiationinareptiledepartsfromtheclassicalamniotemodel AT marshallgravesjennifera geneexpressionofmalepathwaygenessox9andamhduringearlysexdifferentiationinareptiledepartsfromtheclassicalamniotemodel AT georgesarthur geneexpressionofmalepathwaygenessox9andamhduringearlysexdifferentiationinareptiledepartsfromtheclassicalamniotemodel |