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A male-specific doublesex isoform reveals an evolutionary pathway of sexual development via distinct alternative splicing mechanisms
The doublesex/mab-3 related transcription factor (Dmrt) genes regulate sexual development in metazoans. Studies of the doublesex (dsx) gene in insects, in particular Drosophila melanogaster, reveal that alternative splicing of dsx generates sex-specific Dsx isoforms underlying sexual differentiation...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307624/ https://www.ncbi.nlm.nih.gov/pubmed/35869175 http://dx.doi.org/10.1038/s42003-022-03664-7 |
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author | Han, Caihong Peng, Qionglin Su, Xiangbin Xing, Limin Ji, Xiaoxiao Pan, Yufeng |
author_facet | Han, Caihong Peng, Qionglin Su, Xiangbin Xing, Limin Ji, Xiaoxiao Pan, Yufeng |
author_sort | Han, Caihong |
collection | PubMed |
description | The doublesex/mab-3 related transcription factor (Dmrt) genes regulate sexual development in metazoans. Studies of the doublesex (dsx) gene in insects, in particular Drosophila melanogaster, reveal that alternative splicing of dsx generates sex-specific Dsx isoforms underlying sexual differentiation. Such a splicing-based mechanism underlying sex-specific Dmrt function is thought to be evolved from a transcription-based mechanism used in non-insect species, but how such transition occurs during evolution is not known. Here we identified a male-specific dsx transcript (dsx(M2)) through intron retention (IR), in addition to previously identified dsx(M) and dsx(F) transcripts through alternative polyadenylation (APA) with mutually exclusive exons. We found that Dsx(M2) had similarly masculinizing function as Dsx(M). We also found that the IR-based mechanism generating sex-specific dsx transcripts was conserved from flies to cockroaches. Further analysis of these dsx transcripts suggested an evolutionary pathway from sexually monomorphic to sex-specific dsx via the sequential use of IR-based and APA-based alternative splicing. |
format | Online Article Text |
id | pubmed-9307624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93076242022-07-24 A male-specific doublesex isoform reveals an evolutionary pathway of sexual development via distinct alternative splicing mechanisms Han, Caihong Peng, Qionglin Su, Xiangbin Xing, Limin Ji, Xiaoxiao Pan, Yufeng Commun Biol Article The doublesex/mab-3 related transcription factor (Dmrt) genes regulate sexual development in metazoans. Studies of the doublesex (dsx) gene in insects, in particular Drosophila melanogaster, reveal that alternative splicing of dsx generates sex-specific Dsx isoforms underlying sexual differentiation. Such a splicing-based mechanism underlying sex-specific Dmrt function is thought to be evolved from a transcription-based mechanism used in non-insect species, but how such transition occurs during evolution is not known. Here we identified a male-specific dsx transcript (dsx(M2)) through intron retention (IR), in addition to previously identified dsx(M) and dsx(F) transcripts through alternative polyadenylation (APA) with mutually exclusive exons. We found that Dsx(M2) had similarly masculinizing function as Dsx(M). We also found that the IR-based mechanism generating sex-specific dsx transcripts was conserved from flies to cockroaches. Further analysis of these dsx transcripts suggested an evolutionary pathway from sexually monomorphic to sex-specific dsx via the sequential use of IR-based and APA-based alternative splicing. Nature Publishing Group UK 2022-07-22 /pmc/articles/PMC9307624/ /pubmed/35869175 http://dx.doi.org/10.1038/s42003-022-03664-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Han, Caihong Peng, Qionglin Su, Xiangbin Xing, Limin Ji, Xiaoxiao Pan, Yufeng A male-specific doublesex isoform reveals an evolutionary pathway of sexual development via distinct alternative splicing mechanisms |
title | A male-specific doublesex isoform reveals an evolutionary pathway of sexual development via distinct alternative splicing mechanisms |
title_full | A male-specific doublesex isoform reveals an evolutionary pathway of sexual development via distinct alternative splicing mechanisms |
title_fullStr | A male-specific doublesex isoform reveals an evolutionary pathway of sexual development via distinct alternative splicing mechanisms |
title_full_unstemmed | A male-specific doublesex isoform reveals an evolutionary pathway of sexual development via distinct alternative splicing mechanisms |
title_short | A male-specific doublesex isoform reveals an evolutionary pathway of sexual development via distinct alternative splicing mechanisms |
title_sort | male-specific doublesex isoform reveals an evolutionary pathway of sexual development via distinct alternative splicing mechanisms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307624/ https://www.ncbi.nlm.nih.gov/pubmed/35869175 http://dx.doi.org/10.1038/s42003-022-03664-7 |
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