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.

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.