miR-125a-5p increases cellular DNA damage of aging males and perturbs stage-specific embryo development via Rbm38-p53 signaling

Aging Cell. 2021 Dec;20(12):e13508. doi: 10.1111/acel.13508. Epub 2021 Nov 9.

Abstract

An increasing number of men are fathering children at an older age than in the past. While advanced maternal age has long been recognized as a risk factor for adverse reproductive outcomes, the influence of paternal age on reproduction is incompletely comprehended. Herein, we found that miR-125a-5p was upregulated in the sperm of aging males and was related to inferior sperm DNA integrity as an adverse predictor. Moreover, we demonstrated that miR-125a-5p suppressed mitochondrial function and increased cellular DNA damage in GC2 cells. We also found that miR-125a-5p perturbed embryo development at specific morula/blastocyst stages. Mechanistically, we confirmed that miR-125a-5p disturbed the mitochondrial function by targeting Rbm38 and activating the p53 damage response pathway, and induced a developmental delay in a p21-dependent manner. Our study revealed an important role of miR-125a-5p in sperm function and early embryo development of aging males, and provided a fresh view to comprehend the aging process in sperm.

Keywords: DNA damage; Rbm38; male aging; miRNA; sperm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging
  • DNA Damage / genetics*
  • Embryonic Development / genetics*
  • Humans
  • Male
  • MicroRNAs / metabolism*
  • RNA-Binding Proteins / genetics*
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • MIRN125 microRNA, human
  • MicroRNAs
  • RBM38 protein, human
  • RNA-Binding Proteins
  • Tumor Suppressor Protein p53