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Asymmetric interactions between doublesex and tissue- and sex-specific target genes mediate sexual dimorphism in beetles
Sexual dimorphisms fuel significant intraspecific variation and evolutionary diversification. Yet the developmental-genetic mechanisms underlying sex-specific development remain poorly understood. Here, we focus on the conserved sex-determination gene doublesex (dsx) and the mechanisms by which it m...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333360/ https://www.ncbi.nlm.nih.gov/pubmed/28239147 http://dx.doi.org/10.1038/ncomms14593 |
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author | Ledón-Rettig, C. C. Zattara, E. E. Moczek, A. P. |
author_facet | Ledón-Rettig, C. C. Zattara, E. E. Moczek, A. P. |
author_sort | Ledón-Rettig, C. C. |
collection | PubMed |
description | Sexual dimorphisms fuel significant intraspecific variation and evolutionary diversification. Yet the developmental-genetic mechanisms underlying sex-specific development remain poorly understood. Here, we focus on the conserved sex-determination gene doublesex (dsx) and the mechanisms by which it mediates sex-specific development in a horned beetle species by combining systemic dsx knockdown, high-throughput sequencing of diverse tissues and a genome-wide analysis of Dsx-binding sites. We find that Dsx regulates sex-biased expression predominantly in males, that Dsx's target repertoires are highly sex- and tissue-specific and that Dsx can exercise its regulatory role via two distinct mechanisms: as a sex-specific modulator by regulating strictly sex-specific targets, or as a switch by regulating the same genes in males and females in opposite directions. More generally, our results suggest Dsx can rapidly acquire new target gene repertoires to accommodate evolutionarily novel traits, evidenced by the large and unique repertoire identified in head horns, a recent morphological innovation. |
format | Online Article Text |
id | pubmed-5333360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53333602017-03-06 Asymmetric interactions between doublesex and tissue- and sex-specific target genes mediate sexual dimorphism in beetles Ledón-Rettig, C. C. Zattara, E. E. Moczek, A. P. Nat Commun Article Sexual dimorphisms fuel significant intraspecific variation and evolutionary diversification. Yet the developmental-genetic mechanisms underlying sex-specific development remain poorly understood. Here, we focus on the conserved sex-determination gene doublesex (dsx) and the mechanisms by which it mediates sex-specific development in a horned beetle species by combining systemic dsx knockdown, high-throughput sequencing of diverse tissues and a genome-wide analysis of Dsx-binding sites. We find that Dsx regulates sex-biased expression predominantly in males, that Dsx's target repertoires are highly sex- and tissue-specific and that Dsx can exercise its regulatory role via two distinct mechanisms: as a sex-specific modulator by regulating strictly sex-specific targets, or as a switch by regulating the same genes in males and females in opposite directions. More generally, our results suggest Dsx can rapidly acquire new target gene repertoires to accommodate evolutionarily novel traits, evidenced by the large and unique repertoire identified in head horns, a recent morphological innovation. Nature Publishing Group 2017-02-27 /pmc/articles/PMC5333360/ /pubmed/28239147 http://dx.doi.org/10.1038/ncomms14593 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ledón-Rettig, C. C. Zattara, E. E. Moczek, A. P. Asymmetric interactions between doublesex and tissue- and sex-specific target genes mediate sexual dimorphism in beetles |
title | Asymmetric interactions between doublesex and tissue- and sex-specific target genes mediate sexual dimorphism in beetles |
title_full | Asymmetric interactions between doublesex and tissue- and sex-specific target genes mediate sexual dimorphism in beetles |
title_fullStr | Asymmetric interactions between doublesex and tissue- and sex-specific target genes mediate sexual dimorphism in beetles |
title_full_unstemmed | Asymmetric interactions between doublesex and tissue- and sex-specific target genes mediate sexual dimorphism in beetles |
title_short | Asymmetric interactions between doublesex and tissue- and sex-specific target genes mediate sexual dimorphism in beetles |
title_sort | asymmetric interactions between doublesex and tissue- and sex-specific target genes mediate sexual dimorphism in beetles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333360/ https://www.ncbi.nlm.nih.gov/pubmed/28239147 http://dx.doi.org/10.1038/ncomms14593 |
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