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Published on: January 14, 2021
Prmt7 Downregulation in Mouse Spermatogonia Functions through miR-877-3p/Col6a3
Hongmei Gao1, Mingrui Zhang1,2, Jiankang Guo1
1Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Abstract:
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.
Insights
Protein arginine methyltransferases 7 (Prmt7) plays a role in male germ cell proliferation. Prmt7 downregulation affects miRNA expression, potentially impacting spermatogonial development via the miR-877-3p/Col6a3 pathway.
Area of Science:
- Reproductive Biology
- Molecular Endocrinology
- Epigenetics
Background:
- Protein arginine methyltransferases 7 (Prmt7) is vital in male germ cells.
- Prmt7 downregulation impairs spermatogonial proliferation.
- The regulatory mechanism involving microRNAs (miRNAs) and target genes remains unclear.
Purpose of the Study:
- To investigate the role of Prmt7 in regulating spermatogonial proliferation through miRNA.
- To identify Prmt7-responsive miRNAs and their target genes in mouse spermatogonia.
Main Methods:
- Experimental Prmt7 knockdown in GC-1 cells.
- miRNA sequencing to identify differentially expressed miRNAs (DEmiRNAs).
- Quantitative reverse transcription PCR (qRT-PCR) for validation.
- Bioinformatic prediction of miRNA target genes.
Main Results:
- Identified 48 DEmiRNAs (36 upregulated, 12 downregulated) in response to Prmt7 reduction.
- Confirmed seven miRNA/target gene pairs potentially regulated by Prmt7.
- Identified Col6a3 as a target gene of mmu-miR-877-3p.
Conclusions:
- Prmt7 downregulation in mouse spermatogonia may operate via the miR-877-3p/Col6a3 axis.
- Provides novel insights into Prmt7's function in male germ cell development mediated by miRNAs.

