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Unexpected mutual regulation underlies paralogue functional diversification and promotes epithelial tissue maturation in Tribolium
Insect Hox3/zen genes represent an evolutionary hotspot for changes in function and copy number. Single orthologues are required either for early specification or late morphogenesis of the extraembryonic tissues, which protect the embryo. The tandemly duplicated zen paralogues of the beetle Triboliu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536231/ https://www.ncbi.nlm.nih.gov/pubmed/33020571 http://dx.doi.org/10.1038/s42003-020-01250-3 |
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author | Gurska, Daniela Vargas Jentzsch, Iris M. Panfilio, Kristen A. |
author_facet | Gurska, Daniela Vargas Jentzsch, Iris M. Panfilio, Kristen A. |
author_sort | Gurska, Daniela |
collection | PubMed |
description | Insect Hox3/zen genes represent an evolutionary hotspot for changes in function and copy number. Single orthologues are required either for early specification or late morphogenesis of the extraembryonic tissues, which protect the embryo. The tandemly duplicated zen paralogues of the beetle Tribolium castaneum present a unique opportunity to investigate both functions in a single species. We dissect the paralogues’ expression dynamics (transcript and protein) and transcriptional targets (RNA-seq after RNAi) throughout embryogenesis. We identify an unexpected role of Tc-Zen2 in repression of Tc-zen1, generating a negative feedback loop that promotes developmental progression. Tc-Zen2 regulation is dynamic, including within co-expressed multigene loci. We also show that extraembryonic development is the major event within the transcriptional landscape of late embryogenesis and provide a global molecular characterization of the extraembryonic serosal tissue. Altogether, we propose that paralogue mutual regulation arose through multiple instances of zen subfunctionalization, leading to their complementary extant roles. |
format | Online Article Text |
id | pubmed-7536231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75362312020-10-19 Unexpected mutual regulation underlies paralogue functional diversification and promotes epithelial tissue maturation in Tribolium Gurska, Daniela Vargas Jentzsch, Iris M. Panfilio, Kristen A. Commun Biol Article Insect Hox3/zen genes represent an evolutionary hotspot for changes in function and copy number. Single orthologues are required either for early specification or late morphogenesis of the extraembryonic tissues, which protect the embryo. The tandemly duplicated zen paralogues of the beetle Tribolium castaneum present a unique opportunity to investigate both functions in a single species. We dissect the paralogues’ expression dynamics (transcript and protein) and transcriptional targets (RNA-seq after RNAi) throughout embryogenesis. We identify an unexpected role of Tc-Zen2 in repression of Tc-zen1, generating a negative feedback loop that promotes developmental progression. Tc-Zen2 regulation is dynamic, including within co-expressed multigene loci. We also show that extraembryonic development is the major event within the transcriptional landscape of late embryogenesis and provide a global molecular characterization of the extraembryonic serosal tissue. Altogether, we propose that paralogue mutual regulation arose through multiple instances of zen subfunctionalization, leading to their complementary extant roles. Nature Publishing Group UK 2020-10-05 /pmc/articles/PMC7536231/ /pubmed/33020571 http://dx.doi.org/10.1038/s42003-020-01250-3 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Gurska, Daniela Vargas Jentzsch, Iris M. Panfilio, Kristen A. Unexpected mutual regulation underlies paralogue functional diversification and promotes epithelial tissue maturation in Tribolium |
title | Unexpected mutual regulation underlies paralogue functional diversification and promotes epithelial tissue maturation in Tribolium |
title_full | Unexpected mutual regulation underlies paralogue functional diversification and promotes epithelial tissue maturation in Tribolium |
title_fullStr | Unexpected mutual regulation underlies paralogue functional diversification and promotes epithelial tissue maturation in Tribolium |
title_full_unstemmed | Unexpected mutual regulation underlies paralogue functional diversification and promotes epithelial tissue maturation in Tribolium |
title_short | Unexpected mutual regulation underlies paralogue functional diversification and promotes epithelial tissue maturation in Tribolium |
title_sort | unexpected mutual regulation underlies paralogue functional diversification and promotes epithelial tissue maturation in tribolium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536231/ https://www.ncbi.nlm.nih.gov/pubmed/33020571 http://dx.doi.org/10.1038/s42003-020-01250-3 |
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