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Somatic CG6015 mediates cyst stem cell maintenance and germline stem cell differentiation via EGFR signaling in Drosophila testes

Stem cell niche is regulated by intrinsic and extrinsic factors. In the Drosophila testis, cyst stem cells (CySCs) support the differentiation of germline stem cells (GSCs). However, the underlying mechanisms remain unclear. In this study, we found that somatic CG6015 is required for CySC maintenanc...

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Autores principales: Zheng, Qianwen, Chen, Xia, Qiao, Chen, Wang, Min, Chen, Wanyin, Luan, Xiaojin, Yan, Yidan, Shen, Cong, Fang, Jie, Hu, Xing, Zheng, Bo, Wu, Yibo, Yu, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024382/
https://www.ncbi.nlm.nih.gov/pubmed/33824283
http://dx.doi.org/10.1038/s41420-021-00452-w
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author Zheng, Qianwen
Chen, Xia
Qiao, Chen
Wang, Min
Chen, Wanyin
Luan, Xiaojin
Yan, Yidan
Shen, Cong
Fang, Jie
Hu, Xing
Zheng, Bo
Wu, Yibo
Yu, Jun
author_facet Zheng, Qianwen
Chen, Xia
Qiao, Chen
Wang, Min
Chen, Wanyin
Luan, Xiaojin
Yan, Yidan
Shen, Cong
Fang, Jie
Hu, Xing
Zheng, Bo
Wu, Yibo
Yu, Jun
author_sort Zheng, Qianwen
collection PubMed
description Stem cell niche is regulated by intrinsic and extrinsic factors. In the Drosophila testis, cyst stem cells (CySCs) support the differentiation of germline stem cells (GSCs). However, the underlying mechanisms remain unclear. In this study, we found that somatic CG6015 is required for CySC maintenance and GSC differentiation in a Drosophila model. Knockdown of CG6015 in CySCs caused aberrant activation of dpERK in undifferentiated germ cells in the Drosophila testis, and disruption of key downstream targets of EGFR signaling (Dsor1 and rl) in CySCs results in a phenotype resembling that of CG6015 knockdown. CG6015, Dsor1, and rl are essential for the survival of Drosophila cell line Schneider 2 (S2) cells. Our data showed that somatic CG6015 regulates CySC maintenance and GSC differentiation via EGFR signaling, and inhibits aberrant activation of germline dpERK signals. These findings indicate regulatory mechanisms of stem cell niche homeostasis in the Drosophila testis.
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spelling pubmed-80243822021-04-21 Somatic CG6015 mediates cyst stem cell maintenance and germline stem cell differentiation via EGFR signaling in Drosophila testes Zheng, Qianwen Chen, Xia Qiao, Chen Wang, Min Chen, Wanyin Luan, Xiaojin Yan, Yidan Shen, Cong Fang, Jie Hu, Xing Zheng, Bo Wu, Yibo Yu, Jun Cell Death Discov Article Stem cell niche is regulated by intrinsic and extrinsic factors. In the Drosophila testis, cyst stem cells (CySCs) support the differentiation of germline stem cells (GSCs). However, the underlying mechanisms remain unclear. In this study, we found that somatic CG6015 is required for CySC maintenance and GSC differentiation in a Drosophila model. Knockdown of CG6015 in CySCs caused aberrant activation of dpERK in undifferentiated germ cells in the Drosophila testis, and disruption of key downstream targets of EGFR signaling (Dsor1 and rl) in CySCs results in a phenotype resembling that of CG6015 knockdown. CG6015, Dsor1, and rl are essential for the survival of Drosophila cell line Schneider 2 (S2) cells. Our data showed that somatic CG6015 regulates CySC maintenance and GSC differentiation via EGFR signaling, and inhibits aberrant activation of germline dpERK signals. These findings indicate regulatory mechanisms of stem cell niche homeostasis in the Drosophila testis. Nature Publishing Group UK 2021-04-06 /pmc/articles/PMC8024382/ /pubmed/33824283 http://dx.doi.org/10.1038/s41420-021-00452-w Text en © The Author(s) 2021 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
Zheng, Qianwen
Chen, Xia
Qiao, Chen
Wang, Min
Chen, Wanyin
Luan, Xiaojin
Yan, Yidan
Shen, Cong
Fang, Jie
Hu, Xing
Zheng, Bo
Wu, Yibo
Yu, Jun
Somatic CG6015 mediates cyst stem cell maintenance and germline stem cell differentiation via EGFR signaling in Drosophila testes
title Somatic CG6015 mediates cyst stem cell maintenance and germline stem cell differentiation via EGFR signaling in Drosophila testes
title_full Somatic CG6015 mediates cyst stem cell maintenance and germline stem cell differentiation via EGFR signaling in Drosophila testes
title_fullStr Somatic CG6015 mediates cyst stem cell maintenance and germline stem cell differentiation via EGFR signaling in Drosophila testes
title_full_unstemmed Somatic CG6015 mediates cyst stem cell maintenance and germline stem cell differentiation via EGFR signaling in Drosophila testes
title_short Somatic CG6015 mediates cyst stem cell maintenance and germline stem cell differentiation via EGFR signaling in Drosophila testes
title_sort somatic cg6015 mediates cyst stem cell maintenance and germline stem cell differentiation via egfr signaling in drosophila testes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024382/
https://www.ncbi.nlm.nih.gov/pubmed/33824283
http://dx.doi.org/10.1038/s41420-021-00452-w
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