Rnf138 deficiency promotes apoptosis of spermatogonia in juvenile male mice

Cell Death Dis. 2017 May 18;8(5):e2795. doi: 10.1038/cddis.2017.110.

Abstract

Spermatogenesis, the process by which haploid sperm cells are produced from a diploid precursor cell, is essential for sexual reproduction. Here, we report that RING-finger protein 138 (Rnf138) is highly expressed in testes, especially in spermatogonia and spermatocytes. The role of Rnf138 in spermatogenesis was examined using a Rnf138-knockout mouse model. Rnf138 deficiency resulted in increased apoptosis in spermatogenic cells, loss of proliferative spermatogonia, delayed development of spermatozoa and impaired fertility. The proportion of PLZF+Ki67+ cells within the PLZF+ population decreased in the knockout mice. The phenotype was further assessed by RNA-sequencing (RNA-seq), which determined that the expression levels of many genes involved in spermatogenesis were altered in the testis of Rnf138-knockout mice. Thus, Rnf138 deficiency promotes the apoptosis of spermatogenic cells, which may have been caused by the aberrant proliferation of spermatogonia in mouse testis development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis* / genetics
  • Cell Differentiation
  • Cell Proliferation
  • Gene Deletion
  • Gene Expression Regulation
  • Gene Ontology
  • Male
  • Meiosis
  • Mice, Knockout
  • Recombination, Genetic / genetics
  • Spermatogenesis
  • Spermatogonia / cytology*
  • Spermatogonia / metabolism
  • Testis / metabolism
  • Time Factors
  • Ubiquitin-Protein Ligases / deficiency*
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • RNF138 protein, mouse
  • Ubiquitin-Protein Ligases