Bta-miR-6531 Regulates Calcium Influx in Bovine Leydig Cells and Is Associated with Sperm Motility

Genes (Basel). 2022 Oct 3;13(10):1788. doi: 10.3390/genes13101788.

Abstract

MicroRNAs (miRNAs) play key roles in sperm as the regulatory factors involved in fertility and subsequent early embryonic development. Bta-miR-6531 is specifically a highly enriched miRNA in low-motility sperms in previous study. To investigate the mechanism of bta-miR-6531, 508 shared target genes of bta-miR-6531 were predicted using two miRNA target databases (TargetScan7 and miRWalk). According to the Kyoto Encyclopedia of Genes and Genomes (KEGG), the calcium and cAMP signaling pathways were the most enriched of the target genes. A dual-luciferase assay indicated that bta-miR-6531 targeted ATP2A2 mRNA by binding to the coding sequence region. In bovine Leydig cells, bta-miR-6531 overexpression affected the intracellular calcium concentration by restraining ATP2A2 expression. Moreover, we observed high calcium concentrations and high ATP2A2 protein levels in high-motility sperm compared with those in low-motility sperms. Furthermore, high-linkage single-nucleotide polymorphisms (SNPs) of the pre-bta-miR-6531 sequence were identified that related to sperm traits. Genotype TCTC of bta-miR-6531 showed high sperm motility and density and low deformity rate in Holstein bulls. However, the mutation in pre-miR-6531 did not significantly affect mature bta-miR-6531 expression in the sperm or cell models. Our results demonstrate that bta-miR-6531 might involve in sperm motility regulation by targeting ATP2A2 of the calcium signaling pathway in bovine spermatozoa.

Keywords: ATP2A2; SNP; bta-miR-6531; calcium signaling pathway; sperm motility.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium*
  • Cattle
  • Leydig Cells / metabolism
  • Male
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • RNA, Messenger
  • Semen / metabolism
  • Sperm Motility / genetics

Substances

  • Calcium
  • MicroRNAs
  • RNA, Messenger

Grants and funding

This research was funded by the National Natural Science Foundation of China (31871248), Jiangsu Postdoctoral Science Foundation (2021K001A) and Jiangsu Provincial Key Research and Development Program (BE2021372).