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G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice

BACKGROUND: Spermatogenesis is a complex process that includes mitosis, meiosis, and spermiogenesis. During spermatogenesis, genetic factors play a vital role inthe formation of properly functioning sperm. GTPase-activating protein (SH3 domain)-binding protein 2 (G3BP2) is known to take part in immu...

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Autores principales: Yun, Damin, Zhou, Liwei, Shi, Jie, Li, Xinyao, Wu, Xiaolong, Sun, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248785/
https://www.ncbi.nlm.nih.gov/pubmed/35782098
http://dx.doi.org/10.7717/peerj.13532
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author Yun, Damin
Zhou, Liwei
Shi, Jie
Li, Xinyao
Wu, Xiaolong
Sun, Fei
author_facet Yun, Damin
Zhou, Liwei
Shi, Jie
Li, Xinyao
Wu, Xiaolong
Sun, Fei
author_sort Yun, Damin
collection PubMed
description BACKGROUND: Spermatogenesis is a complex process that includes mitosis, meiosis, and spermiogenesis. During spermatogenesis, genetic factors play a vital role inthe formation of properly functioning sperm. GTPase-activating protein (SH3 domain)-binding protein 2 (G3BP2) is known to take part in immune responses, mRNA transport, and stress-granule assembly. However, its role in male fertility is unclear. Here, we generated a G3bp2 conditional knockout (cKO) mouse model to explore the function of G3BP2 in male fertility. METHODS: Polymerase chain reaction (PCR) and western blotting (WB) were used to confirm testis-specific G3bp2 knockout. Hematoxylin-eosin (HE) staining to observe testicular morphology and epididymal structure. Computer-aided sperm analysis (CASA) to detect sperm concentration and motility. Terminal deoxynucleotidyl transferase-dUTP nick-end labeling (TUNEL) assay was used to detect apoptotic cells. RESULTS: We found that cKO male mice are fertile with the normal morphology of the testis and sperm. Additionally, CASA of the semen from cKO mice showed that they all had a similar sperm concentration and motility. In addition, sperm from these mice exhibited a similar morphology. But the tunnel assay revealed increased apoptosis in their testes relative to the level in the wild type (WT). CONCLUSION: Together, our data demonstrate that G3BP2 is dispensable for spermatogenesis and male fertility in mice albeit with the increased germ-cell apoptosis.
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spelling pubmed-92487852022-07-02 G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice Yun, Damin Zhou, Liwei Shi, Jie Li, Xinyao Wu, Xiaolong Sun, Fei PeerJ Cell Biology BACKGROUND: Spermatogenesis is a complex process that includes mitosis, meiosis, and spermiogenesis. During spermatogenesis, genetic factors play a vital role inthe formation of properly functioning sperm. GTPase-activating protein (SH3 domain)-binding protein 2 (G3BP2) is known to take part in immune responses, mRNA transport, and stress-granule assembly. However, its role in male fertility is unclear. Here, we generated a G3bp2 conditional knockout (cKO) mouse model to explore the function of G3BP2 in male fertility. METHODS: Polymerase chain reaction (PCR) and western blotting (WB) were used to confirm testis-specific G3bp2 knockout. Hematoxylin-eosin (HE) staining to observe testicular morphology and epididymal structure. Computer-aided sperm analysis (CASA) to detect sperm concentration and motility. Terminal deoxynucleotidyl transferase-dUTP nick-end labeling (TUNEL) assay was used to detect apoptotic cells. RESULTS: We found that cKO male mice are fertile with the normal morphology of the testis and sperm. Additionally, CASA of the semen from cKO mice showed that they all had a similar sperm concentration and motility. In addition, sperm from these mice exhibited a similar morphology. But the tunnel assay revealed increased apoptosis in their testes relative to the level in the wild type (WT). CONCLUSION: Together, our data demonstrate that G3BP2 is dispensable for spermatogenesis and male fertility in mice albeit with the increased germ-cell apoptosis. PeerJ Inc. 2022-06-28 /pmc/articles/PMC9248785/ /pubmed/35782098 http://dx.doi.org/10.7717/peerj.13532 Text en © 2022 Yun et al. 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, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Cell Biology
Yun, Damin
Zhou, Liwei
Shi, Jie
Li, Xinyao
Wu, Xiaolong
Sun, Fei
G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice
title G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice
title_full G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice
title_fullStr G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice
title_full_unstemmed G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice
title_short G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice
title_sort g3bp2, a stress granule assembly factor, is dispensable for spermatogenesis in mice
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248785/
https://www.ncbi.nlm.nih.gov/pubmed/35782098
http://dx.doi.org/10.7717/peerj.13532
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