Ccdc117 deficiency triggers compensatory hyperandrogenism to sustain spermatogenesis and male fertility

Methods

We generated a Ccdc117 knockout mouse model using CRISPR/Cas9 and characterized the phenotypic consequences through histology, computer-assisted sperm analysis (CASA), and fertility assessments. The molecular underpinnings were investigated via testis-wide RNA sequencing, Western blotting, immunofluorescence, and hormonal measurements. Results Ccdc117ko males developed a paradoxical phenotype: significant testicular hypotrophy alongside completely preserved fertility.

Despite a ~25% reduction in testis size, sperm counts, motility, and spermatogenic progression were normal. Transcriptomic analysis uncovered a specific and coordinated upregulation of the steroidogenic pathway, which was validated by a concomitant increase in the protein levels of key enzymes (CYP17A1, StAR, HSD3B2) specifically within Leydig cells. Consequently, serum testosterone levels were significantly elevated by approximately two-fold without a concomitant rise in GnRH.