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Prmt7 Downregulation in Mouse Spermatogonia Functions through miR-877-3p/Col6a3
Protein arginine methyltransferases 7 (Prmt7) is expressed in male germ cells, including primordial germ cells, gonocytes, and spermatogonia. Our previous study demonstrated that Prmt7 downregulation reduced the proliferation of GC-1 cells (a cell line of mouse immortalized spermatogonia). However,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410080/ https://www.ncbi.nlm.nih.gov/pubmed/36013373 http://dx.doi.org/10.3390/life12081194 |
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author | Gao, Hongmei Zhang, Mingrui Guo, Jiankang Liu, Zhiguo Guo, Fei Wang, Bingyuan Mu, Yulian |
author_facet | Gao, Hongmei Zhang, Mingrui Guo, Jiankang Liu, Zhiguo Guo, Fei Wang, Bingyuan Mu, Yulian |
author_sort | Gao, Hongmei |
collection | PubMed |
description | Protein arginine methyltransferases 7 (Prmt7) is expressed in male germ cells, including primordial germ cells, gonocytes, and spermatogonia. Our previous study demonstrated that Prmt7 downregulation reduced the proliferation of GC-1 cells (a cell line of mouse immortalized spermatogonia). However, how Prmt7 regulates spermatogonial proliferation through miRNA and the target gene remains elusive. Here, we experimentally reduced the Prmt7 expression in the GC-1 cells and subjected them to miRNA sequencing to explore the miRNA profile and its Prmt7-responsive members. In total, 48 differentially expressed miRNAs (DEmiRNAs), including 36 upregulated and 12 downregulated miRNAs, were identified. After verifying the validity of sequencing results through qRT-PCR assays in randomly selected DEmiRNAs, we predicted the target genes of these DEmiRNAs. Next, we combined DEmiRNA target genes and previously identified differentially expressed genes between Prmt7 knockdown and control groups of GC-1 cells, which resulted in seven miRNA/target gene pairs. Among these miRNA/target gene pairs, we further detected the expression of Col6a3 (collagen type VI alpha 3) as the target gene of mmu-miR-877-3p. The results suggested that Prmt7 downregulation in mouse spermatogonia might function through miR-877-3p/Col6a3. Overall, these findings provide new insights into the role of Prmt7 in male germ cell development through miRNA and target genes. |
format | Online Article Text |
id | pubmed-9410080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94100802022-08-26 Prmt7 Downregulation in Mouse Spermatogonia Functions through miR-877-3p/Col6a3 Gao, Hongmei Zhang, Mingrui Guo, Jiankang Liu, Zhiguo Guo, Fei Wang, Bingyuan Mu, Yulian Life (Basel) Article Protein arginine methyltransferases 7 (Prmt7) is expressed in male germ cells, including primordial germ cells, gonocytes, and spermatogonia. Our previous study demonstrated that Prmt7 downregulation reduced the proliferation of GC-1 cells (a cell line of mouse immortalized spermatogonia). However, how Prmt7 regulates spermatogonial proliferation through miRNA and the target gene remains elusive. Here, we experimentally reduced the Prmt7 expression in the GC-1 cells and subjected them to miRNA sequencing to explore the miRNA profile and its Prmt7-responsive members. In total, 48 differentially expressed miRNAs (DEmiRNAs), including 36 upregulated and 12 downregulated miRNAs, were identified. After verifying the validity of sequencing results through qRT-PCR assays in randomly selected DEmiRNAs, we predicted the target genes of these DEmiRNAs. Next, we combined DEmiRNA target genes and previously identified differentially expressed genes between Prmt7 knockdown and control groups of GC-1 cells, which resulted in seven miRNA/target gene pairs. Among these miRNA/target gene pairs, we further detected the expression of Col6a3 (collagen type VI alpha 3) as the target gene of mmu-miR-877-3p. The results suggested that Prmt7 downregulation in mouse spermatogonia might function through miR-877-3p/Col6a3. Overall, these findings provide new insights into the role of Prmt7 in male germ cell development through miRNA and target genes. MDPI 2022-08-05 /pmc/articles/PMC9410080/ /pubmed/36013373 http://dx.doi.org/10.3390/life12081194 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gao, Hongmei Zhang, Mingrui Guo, Jiankang Liu, Zhiguo Guo, Fei Wang, Bingyuan Mu, Yulian Prmt7 Downregulation in Mouse Spermatogonia Functions through miR-877-3p/Col6a3 |
title | Prmt7 Downregulation in Mouse Spermatogonia Functions through miR-877-3p/Col6a3 |
title_full | Prmt7 Downregulation in Mouse Spermatogonia Functions through miR-877-3p/Col6a3 |
title_fullStr | Prmt7 Downregulation in Mouse Spermatogonia Functions through miR-877-3p/Col6a3 |
title_full_unstemmed | Prmt7 Downregulation in Mouse Spermatogonia Functions through miR-877-3p/Col6a3 |
title_short | Prmt7 Downregulation in Mouse Spermatogonia Functions through miR-877-3p/Col6a3 |
title_sort | prmt7 downregulation in mouse spermatogonia functions through mir-877-3p/col6a3 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410080/ https://www.ncbi.nlm.nih.gov/pubmed/36013373 http://dx.doi.org/10.3390/life12081194 |
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