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The pluripotency factor Tex10 finetunes Wnt signaling for PGC and male germline development
Testis-specific transcript 10 (Tex10) is a critical factor for pluripotent stem cell maintenance and preimplantation development. Here, we dissect its late developmental roles in primordial germ cell (PGC) specification and spermatogenesis using cellular and animal models. We discover that Tex10 bin...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980098/ https://www.ncbi.nlm.nih.gov/pubmed/36865339 http://dx.doi.org/10.1101/2023.02.23.529824 |
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author | Li, Dan Yang, Jihong Ma, Fanglin Malik, Vikas Zang, Ruge Shi, Xianle Huang, Xin Zhou, Hongwei Wang, Jianlong |
author_facet | Li, Dan Yang, Jihong Ma, Fanglin Malik, Vikas Zang, Ruge Shi, Xianle Huang, Xin Zhou, Hongwei Wang, Jianlong |
author_sort | Li, Dan |
collection | PubMed |
description | Testis-specific transcript 10 (Tex10) is a critical factor for pluripotent stem cell maintenance and preimplantation development. Here, we dissect its late developmental roles in primordial germ cell (PGC) specification and spermatogenesis using cellular and animal models. We discover that Tex10 binds the Wnt negative regulator genes, marked by H3K4me3, at the PGC-like cell (PGCLC) stage in restraining Wnt signaling. Depletion and overexpression of Tex10 hyperactivate and attenuate the Wnt signaling, resulting in compromised and enhanced PGCLC specification efficiency, respectively. Using the Tex10 conditional knockout mouse models combined with single-cell RNA sequencing, we further uncover critical roles of Tex10 in spermatogenesis with Tex10 loss causing reduced sperm number and motility associated with compromised round spermatid formation. Notably, defective spermatogenesis in Tex10 knockout mice correlates with aberrant Wnt signaling upregulation. Therefore, our study establishes Tex10 as a previously unappreciated player in PGC specification and male germline development by fine-tuning Wnt signaling. |
format | Online Article Text |
id | pubmed-9980098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-99800982023-03-03 The pluripotency factor Tex10 finetunes Wnt signaling for PGC and male germline development Li, Dan Yang, Jihong Ma, Fanglin Malik, Vikas Zang, Ruge Shi, Xianle Huang, Xin Zhou, Hongwei Wang, Jianlong bioRxiv Article Testis-specific transcript 10 (Tex10) is a critical factor for pluripotent stem cell maintenance and preimplantation development. Here, we dissect its late developmental roles in primordial germ cell (PGC) specification and spermatogenesis using cellular and animal models. We discover that Tex10 binds the Wnt negative regulator genes, marked by H3K4me3, at the PGC-like cell (PGCLC) stage in restraining Wnt signaling. Depletion and overexpression of Tex10 hyperactivate and attenuate the Wnt signaling, resulting in compromised and enhanced PGCLC specification efficiency, respectively. Using the Tex10 conditional knockout mouse models combined with single-cell RNA sequencing, we further uncover critical roles of Tex10 in spermatogenesis with Tex10 loss causing reduced sperm number and motility associated with compromised round spermatid formation. Notably, defective spermatogenesis in Tex10 knockout mice correlates with aberrant Wnt signaling upregulation. Therefore, our study establishes Tex10 as a previously unappreciated player in PGC specification and male germline development by fine-tuning Wnt signaling. Cold Spring Harbor Laboratory 2023-02-24 /pmc/articles/PMC9980098/ /pubmed/36865339 http://dx.doi.org/10.1101/2023.02.23.529824 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Li, Dan Yang, Jihong Ma, Fanglin Malik, Vikas Zang, Ruge Shi, Xianle Huang, Xin Zhou, Hongwei Wang, Jianlong The pluripotency factor Tex10 finetunes Wnt signaling for PGC and male germline development |
title | The pluripotency factor Tex10 finetunes Wnt signaling for PGC and male germline development |
title_full | The pluripotency factor Tex10 finetunes Wnt signaling for PGC and male germline development |
title_fullStr | The pluripotency factor Tex10 finetunes Wnt signaling for PGC and male germline development |
title_full_unstemmed | The pluripotency factor Tex10 finetunes Wnt signaling for PGC and male germline development |
title_short | The pluripotency factor Tex10 finetunes Wnt signaling for PGC and male germline development |
title_sort | pluripotency factor tex10 finetunes wnt signaling for pgc and male germline development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980098/ https://www.ncbi.nlm.nih.gov/pubmed/36865339 http://dx.doi.org/10.1101/2023.02.23.529824 |
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