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Male-biased protein expression in primordial germ cells, identified through a comparative study of UAS vectors in Drosophila
In Drosophila, three types of UAS vectors (UASt, UASp, and UASz) are currently available for use with the Gal4-UAS system. They have been used successfully in somatic cells and germline cells from ovaries. However, it remains unclear whether they are functional in the germline cells of embryos, larv...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8564522/ https://www.ncbi.nlm.nih.gov/pubmed/34728669 http://dx.doi.org/10.1038/s41598-021-00729-1 |
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author | Masukawa, Masaki Ishizaki, Yuki Miura, Hiroki Hayashi, Makoto Ota, Ryoma Kobayashi, Satoru |
author_facet | Masukawa, Masaki Ishizaki, Yuki Miura, Hiroki Hayashi, Makoto Ota, Ryoma Kobayashi, Satoru |
author_sort | Masukawa, Masaki |
collection | PubMed |
description | In Drosophila, three types of UAS vectors (UASt, UASp, and UASz) are currently available for use with the Gal4-UAS system. They have been used successfully in somatic cells and germline cells from ovaries. However, it remains unclear whether they are functional in the germline cells of embryos, larvae, and adult testes. In this study, we found that all three types of UAS vectors were functional in the germline cells of embryos and larvae and that the UASt and UASz vectors were active in the germline of the distal tip region in adult testes. Moreover, we observed that protein expression from the UAS vectors was male-biased in germline cells of late embryos, whereas their respective mRNA expression levels were not. Furthermore, O-propargyl-puromycin (OPP) staining revealed that protein synthesis was male-biased in these germline cells. In addition, GO terms related to translation and ribosomal maturation were significantly enriched in the male germline. These observations show that translational activity is higher in male than in female germline cells. Therefore, we propose that male-biased protein synthesis may be responsible for the sex differences observed in the early germline. |
format | Online Article Text |
id | pubmed-8564522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85645222021-11-04 Male-biased protein expression in primordial germ cells, identified through a comparative study of UAS vectors in Drosophila Masukawa, Masaki Ishizaki, Yuki Miura, Hiroki Hayashi, Makoto Ota, Ryoma Kobayashi, Satoru Sci Rep Article In Drosophila, three types of UAS vectors (UASt, UASp, and UASz) are currently available for use with the Gal4-UAS system. They have been used successfully in somatic cells and germline cells from ovaries. However, it remains unclear whether they are functional in the germline cells of embryos, larvae, and adult testes. In this study, we found that all three types of UAS vectors were functional in the germline cells of embryos and larvae and that the UASt and UASz vectors were active in the germline of the distal tip region in adult testes. Moreover, we observed that protein expression from the UAS vectors was male-biased in germline cells of late embryos, whereas their respective mRNA expression levels were not. Furthermore, O-propargyl-puromycin (OPP) staining revealed that protein synthesis was male-biased in these germline cells. In addition, GO terms related to translation and ribosomal maturation were significantly enriched in the male germline. These observations show that translational activity is higher in male than in female germline cells. Therefore, we propose that male-biased protein synthesis may be responsible for the sex differences observed in the early germline. Nature Publishing Group UK 2021-11-02 /pmc/articles/PMC8564522/ /pubmed/34728669 http://dx.doi.org/10.1038/s41598-021-00729-1 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 Masukawa, Masaki Ishizaki, Yuki Miura, Hiroki Hayashi, Makoto Ota, Ryoma Kobayashi, Satoru Male-biased protein expression in primordial germ cells, identified through a comparative study of UAS vectors in Drosophila |
title | Male-biased protein expression in primordial germ cells, identified through a comparative study of UAS vectors in Drosophila |
title_full | Male-biased protein expression in primordial germ cells, identified through a comparative study of UAS vectors in Drosophila |
title_fullStr | Male-biased protein expression in primordial germ cells, identified through a comparative study of UAS vectors in Drosophila |
title_full_unstemmed | Male-biased protein expression in primordial germ cells, identified through a comparative study of UAS vectors in Drosophila |
title_short | Male-biased protein expression in primordial germ cells, identified through a comparative study of UAS vectors in Drosophila |
title_sort | male-biased protein expression in primordial germ cells, identified through a comparative study of uas vectors in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8564522/ https://www.ncbi.nlm.nih.gov/pubmed/34728669 http://dx.doi.org/10.1038/s41598-021-00729-1 |
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