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The neuroblast timer gene nubbin exhibits functional redundancy with gap genes to regulate segment identity in Tribolium
The neuroblast timer genes hunchback, Krüppel, nubbin and castor are expressed in temporal sequence in neural stem cells, and in corresponding spatial sequence along the Drosophila blastoderm. As canonical gap genes, hunchback and Krüppel play a crucial role in insect segmentation, but the roles of...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406537/ https://www.ncbi.nlm.nih.gov/pubmed/34351412 http://dx.doi.org/10.1242/dev.199719 |
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author | Tidswell, Olivia R. A. Benton, Matthew A. Akam, Michael |
author_facet | Tidswell, Olivia R. A. Benton, Matthew A. Akam, Michael |
author_sort | Tidswell, Olivia R. A. |
collection | PubMed |
description | The neuroblast timer genes hunchback, Krüppel, nubbin and castor are expressed in temporal sequence in neural stem cells, and in corresponding spatial sequence along the Drosophila blastoderm. As canonical gap genes, hunchback and Krüppel play a crucial role in insect segmentation, but the roles of nubbin and castor in this process remain ambiguous. We have investigated the expression and functions of nubbin and castor during segmentation in the beetle Tribolium. We show that Tc-hunchback, Tc-Krüppel, Tc-nubbin and Tc-castor are expressed sequentially in the segment addition zone, and that Tc-nubbin regulates segment identity redundantly with two previously described gap/gap-like genes, Tc-giant and Tc-knirps. Simultaneous knockdown of Tc-nubbin, Tc-giant and Tc-knirps results in the formation of ectopic legs on abdominal segments. This homeotic transformation is caused by loss of abdominal Hox gene expression, likely due to expanded Tc-Krüppel expression. Our findings support the theory that the neuroblast timer series was co-opted for use in insect segment patterning, and contribute to our growing understanding of the evolution and function of the gap gene network outside of Drosophila. |
format | Online Article Text |
id | pubmed-8406537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-84065372021-09-09 The neuroblast timer gene nubbin exhibits functional redundancy with gap genes to regulate segment identity in Tribolium Tidswell, Olivia R. A. Benton, Matthew A. Akam, Michael Development Research Article The neuroblast timer genes hunchback, Krüppel, nubbin and castor are expressed in temporal sequence in neural stem cells, and in corresponding spatial sequence along the Drosophila blastoderm. As canonical gap genes, hunchback and Krüppel play a crucial role in insect segmentation, but the roles of nubbin and castor in this process remain ambiguous. We have investigated the expression and functions of nubbin and castor during segmentation in the beetle Tribolium. We show that Tc-hunchback, Tc-Krüppel, Tc-nubbin and Tc-castor are expressed sequentially in the segment addition zone, and that Tc-nubbin regulates segment identity redundantly with two previously described gap/gap-like genes, Tc-giant and Tc-knirps. Simultaneous knockdown of Tc-nubbin, Tc-giant and Tc-knirps results in the formation of ectopic legs on abdominal segments. This homeotic transformation is caused by loss of abdominal Hox gene expression, likely due to expanded Tc-Krüppel expression. Our findings support the theory that the neuroblast timer series was co-opted for use in insect segment patterning, and contribute to our growing understanding of the evolution and function of the gap gene network outside of Drosophila. The Company of Biologists Ltd 2021-08-19 /pmc/articles/PMC8406537/ /pubmed/34351412 http://dx.doi.org/10.1242/dev.199719 Text en © 2021. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Tidswell, Olivia R. A. Benton, Matthew A. Akam, Michael The neuroblast timer gene nubbin exhibits functional redundancy with gap genes to regulate segment identity in Tribolium |
title | The neuroblast timer gene nubbin exhibits functional redundancy with gap genes to regulate segment identity in Tribolium |
title_full | The neuroblast timer gene nubbin exhibits functional redundancy with gap genes to regulate segment identity in Tribolium |
title_fullStr | The neuroblast timer gene nubbin exhibits functional redundancy with gap genes to regulate segment identity in Tribolium |
title_full_unstemmed | The neuroblast timer gene nubbin exhibits functional redundancy with gap genes to regulate segment identity in Tribolium |
title_short | The neuroblast timer gene nubbin exhibits functional redundancy with gap genes to regulate segment identity in Tribolium |
title_sort | neuroblast timer gene nubbin exhibits functional redundancy with gap genes to regulate segment identity in tribolium |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406537/ https://www.ncbi.nlm.nih.gov/pubmed/34351412 http://dx.doi.org/10.1242/dev.199719 |
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