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The tumor suppressor archipelago E3 ligase is required for spermatid differentiation in Drosophila testis
The human orthologue of the tumor suppressor protein FBW7 is encoded by the Drosophila archipelago (ago) gene. Ago is an F-box protein that gives substrate specificity to its SCF ubiquitin ligase complex. It has a central role in multiple biological processes in a tissue-specific manner such as cell...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055871/ https://www.ncbi.nlm.nih.gov/pubmed/33875704 http://dx.doi.org/10.1038/s41598-021-87656-3 |
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author | Vedelek, Viktor Kovács, Attila L. Juhász, Gábor Alzyoud, Elham Sinka, Rita |
author_facet | Vedelek, Viktor Kovács, Attila L. Juhász, Gábor Alzyoud, Elham Sinka, Rita |
author_sort | Vedelek, Viktor |
collection | PubMed |
description | The human orthologue of the tumor suppressor protein FBW7 is encoded by the Drosophila archipelago (ago) gene. Ago is an F-box protein that gives substrate specificity to its SCF ubiquitin ligase complex. It has a central role in multiple biological processes in a tissue-specific manner such as cell proliferation, cellular differentiation, hypoxia-induced gene expression. Here we present a previously unknown tissue-specific role of Ago in spermatid differentiation. We identified a classical mutant of ago which is semi-lethal and male-sterile. During the characterization of ago function in testis, we found that ago plays role in spermatid development, following meiosis. We confirmed spermatogenesis defects by silencing ago by RNAi in testes. The ago mutants show multiple abnormalities in elongating and elongated spermatids, including aberration of the cyst morphology, malformed mitochondrial structures, and individualization defects. Additionally, we determined the subcellular localization of Ago protein with mCherry-Ago transgene in spermatids. Our findings highlight the potential roles of Ago in different cellular processes of spermatogenesis, like spermatid individualization, and regulation of mitochondrial morphology. |
format | Online Article Text |
id | pubmed-8055871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80558712021-04-22 The tumor suppressor archipelago E3 ligase is required for spermatid differentiation in Drosophila testis Vedelek, Viktor Kovács, Attila L. Juhász, Gábor Alzyoud, Elham Sinka, Rita Sci Rep Article The human orthologue of the tumor suppressor protein FBW7 is encoded by the Drosophila archipelago (ago) gene. Ago is an F-box protein that gives substrate specificity to its SCF ubiquitin ligase complex. It has a central role in multiple biological processes in a tissue-specific manner such as cell proliferation, cellular differentiation, hypoxia-induced gene expression. Here we present a previously unknown tissue-specific role of Ago in spermatid differentiation. We identified a classical mutant of ago which is semi-lethal and male-sterile. During the characterization of ago function in testis, we found that ago plays role in spermatid development, following meiosis. We confirmed spermatogenesis defects by silencing ago by RNAi in testes. The ago mutants show multiple abnormalities in elongating and elongated spermatids, including aberration of the cyst morphology, malformed mitochondrial structures, and individualization defects. Additionally, we determined the subcellular localization of Ago protein with mCherry-Ago transgene in spermatids. Our findings highlight the potential roles of Ago in different cellular processes of spermatogenesis, like spermatid individualization, and regulation of mitochondrial morphology. Nature Publishing Group UK 2021-04-19 /pmc/articles/PMC8055871/ /pubmed/33875704 http://dx.doi.org/10.1038/s41598-021-87656-3 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Vedelek, Viktor Kovács, Attila L. Juhász, Gábor Alzyoud, Elham Sinka, Rita The tumor suppressor archipelago E3 ligase is required for spermatid differentiation in Drosophila testis |
title | The tumor suppressor archipelago E3 ligase is required for spermatid differentiation in Drosophila testis |
title_full | The tumor suppressor archipelago E3 ligase is required for spermatid differentiation in Drosophila testis |
title_fullStr | The tumor suppressor archipelago E3 ligase is required for spermatid differentiation in Drosophila testis |
title_full_unstemmed | The tumor suppressor archipelago E3 ligase is required for spermatid differentiation in Drosophila testis |
title_short | The tumor suppressor archipelago E3 ligase is required for spermatid differentiation in Drosophila testis |
title_sort | tumor suppressor archipelago e3 ligase is required for spermatid differentiation in drosophila testis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055871/ https://www.ncbi.nlm.nih.gov/pubmed/33875704 http://dx.doi.org/10.1038/s41598-021-87656-3 |
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