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Hemimetabolous insects elucidate the origin of sexual development via alternative splicing

Insects are the only known animals in which sexual differentiation is controlled by sex-specific splicing. The doublesex transcription factor produces distinct male and female isoforms, which are both essential for sex-specific development. dsx splicing depends on transformer, which is also alternat...

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Autores principales: Wexler, Judith, Delaney, Emily Kay, Belles, Xavier, Schal, Coby, Wada-Katsumata, Ayako, Amicucci, Matthew J, Kopp, Artyom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721801/
https://www.ncbi.nlm.nih.gov/pubmed/31478483
http://dx.doi.org/10.7554/eLife.47490
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author Wexler, Judith
Delaney, Emily Kay
Belles, Xavier
Schal, Coby
Wada-Katsumata, Ayako
Amicucci, Matthew J
Kopp, Artyom
author_facet Wexler, Judith
Delaney, Emily Kay
Belles, Xavier
Schal, Coby
Wada-Katsumata, Ayako
Amicucci, Matthew J
Kopp, Artyom
author_sort Wexler, Judith
collection PubMed
description Insects are the only known animals in which sexual differentiation is controlled by sex-specific splicing. The doublesex transcription factor produces distinct male and female isoforms, which are both essential for sex-specific development. dsx splicing depends on transformer, which is also alternatively spliced such that functional Tra is only present in females. This pathway has evolved from an ancestral mechanism where dsx was independent of tra and expressed and required only in males. To reconstruct this transition, we examined three basal, hemimetabolous insect orders: Hemiptera, Phthiraptera, and Blattodea. We show that tra and dsx have distinct functions in these insects, reflecting different stages in the changeover from a transcription-based to a splicing-based mode of sexual differentiation. We propose that the canonical insect tra-dsx pathway evolved via merger between expanding dsx function (from males to both sexes) and narrowing tra function (from a general splicing factor to dedicated regulator of dsx).
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spelling pubmed-67218012019-09-05 Hemimetabolous insects elucidate the origin of sexual development via alternative splicing Wexler, Judith Delaney, Emily Kay Belles, Xavier Schal, Coby Wada-Katsumata, Ayako Amicucci, Matthew J Kopp, Artyom eLife Developmental Biology Insects are the only known animals in which sexual differentiation is controlled by sex-specific splicing. The doublesex transcription factor produces distinct male and female isoforms, which are both essential for sex-specific development. dsx splicing depends on transformer, which is also alternatively spliced such that functional Tra is only present in females. This pathway has evolved from an ancestral mechanism where dsx was independent of tra and expressed and required only in males. To reconstruct this transition, we examined three basal, hemimetabolous insect orders: Hemiptera, Phthiraptera, and Blattodea. We show that tra and dsx have distinct functions in these insects, reflecting different stages in the changeover from a transcription-based to a splicing-based mode of sexual differentiation. We propose that the canonical insect tra-dsx pathway evolved via merger between expanding dsx function (from males to both sexes) and narrowing tra function (from a general splicing factor to dedicated regulator of dsx). eLife Sciences Publications, Ltd 2019-09-03 /pmc/articles/PMC6721801/ /pubmed/31478483 http://dx.doi.org/10.7554/eLife.47490 Text en © 2019, Wexler et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Wexler, Judith
Delaney, Emily Kay
Belles, Xavier
Schal, Coby
Wada-Katsumata, Ayako
Amicucci, Matthew J
Kopp, Artyom
Hemimetabolous insects elucidate the origin of sexual development via alternative splicing
title Hemimetabolous insects elucidate the origin of sexual development via alternative splicing
title_full Hemimetabolous insects elucidate the origin of sexual development via alternative splicing
title_fullStr Hemimetabolous insects elucidate the origin of sexual development via alternative splicing
title_full_unstemmed Hemimetabolous insects elucidate the origin of sexual development via alternative splicing
title_short Hemimetabolous insects elucidate the origin of sexual development via alternative splicing
title_sort hemimetabolous insects elucidate the origin of sexual development via alternative splicing
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721801/
https://www.ncbi.nlm.nih.gov/pubmed/31478483
http://dx.doi.org/10.7554/eLife.47490
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