A nonsense mutation in Ccdc62 gene is responsible for spermiogenesis defects and male infertility in repro29/repro29 mice

Biol Reprod. 2017 Mar 1;96(3):587-597. doi: 10.1095/biolreprod.116.141408.

Abstract

Phenotype-driven mutagenesis is an unbiased method to identify novel genes involved in spermatogenesis and other reproductive processes. Male repro29/repro29 mice generated by the Reproductive Genomics Program at the Jackson Laboratory were infertile with deformed sperm and poor motility. Using selected exonic capture and massively parallel sequencing technologies, we identified a nonsense mutation in the exon 6 of coiled-coil domain-containing 62 gene (Ccdc62), which results in a formation of a premature stop codon and a truncated protein. Among the tissues examined, CCDC62 was found to be expressed at the highest level in mouse testis by reverse transcriptase-PCR (RT-PCR) and Western blot analysis. With immunofluorescent staining, we demonstrated that CCDC62 was expressed in the cytoplasm and the developing acrosome in the spematids of mouse testis, and was specifically localized at the acrosome in mature sperm. The complementation analysis by mating repro29/+ mice with Ccdc62 -/- mice (generated by CRISPR-Cas9 strategy) further provided genetic proof that the infertility of repro29/repro29 mice was caused by Ccdc62 mutation. Finally, it was found that intracellular colocalization and interaction of CCDC62 and Golgi-associated PDZ and coiled-coil motif-containing protein may be important for acrosome formation. Taken together, this study identified a nonsense mutation in Ccdc62, which directly results in male infertility in repro29/repro29 mice.

Keywords: CCDC62; acrosome; male infertility; repro29; spermiogenesis.

MeSH terms

  • Acrosome / physiology
  • Adaptor Proteins, Signal Transducing
  • Animals
  • Base Sequence
  • Carrier Proteins / metabolism
  • Codon, Nonsense
  • Ethylnitrosourea
  • Female
  • Golgi Matrix Proteins
  • Infertility, Male / genetics*
  • Intracellular Signaling Peptides and Proteins
  • Male
  • Mice
  • Mice, Knockout
  • Sequence Analysis, DNA
  • Spermatogenesis / genetics*
  • Testis / growth & development
  • Testis / metabolism
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • CCDC62 protein, mouse
  • Carrier Proteins
  • Codon, Nonsense
  • Golgi Matrix Proteins
  • Gopc protein, mouse
  • Intracellular Signaling Peptides and Proteins
  • Transcription Factors
  • Ethylnitrosourea