ZDHHC5 deficiency impairs spermatogenesis and causes male infertility in mice.
Wang. Zerui Z; Li. Yueming Y; Sun. Shuya S; Chen. Jinyi J; Zheng. Feixiang F; Hu. Zhengwei Z; Zhang. Jintao J; Liu. Bianjiang B; Liu. Mingxi M
Key Findings
- ZDHHC5 knockout mice are completely infertile due to defective spermatogenesis.
- Sperm from knockout mice show reduced count, motility, and structural abnormalities, especially in the tail.
- ZDHHC5 is needed for palmitoylation of IFT81, a protein important for sperm tail development; loss of this modification leads to malformed sperm.
Practical Outcomes
- For the biohacker community, this study offers no direct, actionable protocol or supplement recommendation. It simply highlights that interfering with ZDHHC5‑mediated palmitoylation can impair male fertility, suggesting caution if exploring ways to modulate protein palmitoylation without solid safety data.
Summary
Scientists removed a gene called ZDHHC5 in mice and found the males became completely infertile. The sperm were fewer, moved poorly, and had abnormal shapes. The problem was linked to a missing protein modification (palmitoylation) needed for proper sperm tail formation, and the infertility could be rescued only by directly injecting sperm into eggs (ICSI).
Abstract
S-palmitoylation is a key protein modification, but the role of ZDHHC5 in male fertility was unknown. This study shows ZDHHC5 loss impairs spermatogenesis, causing male infertility, and identifies ZDHHC5 as a key regulator, offering new insights into infertility mechanisms. S-palmitoylation is a reversible post-translational modification critical for protein localization and function. ZDHHC5, a member of the ZDHHC family of palmitoyltransferases, has well-established roles in cardiovascular, neural, and metabolic systems, but its function in male reproduction remains unclear. To investigate this, we generated Zdhhc5-knockout (KO) mice using CRISPR/Cas9 and found that male KO mice exhibited complete infertility. Phenotypic analysis revealed significantly reduced testis-to-body weight ratios, decreased sperm count and motility, and increased sperm malformations, including abnormal heads and folded tails. Histological and ultrastructural analyses demonstrated defective spermatogenesis, with aberrant retention of sperm during seminiferous tubule maturation and abnormal membranous structures in sperm. Immunofluorescence showed that ZDHHC5 predominantly localizes to the Golgi apparatus of round spermatids (steps 2-8) without affecting Golgi morphology or acrosome biogenesis. While in vitro fertilization with Zdhhc5 -/- sperm failed, intracytoplasmic sperm injection (ICSI) successfully rescued male infertility, suggesting functional disruption at the protein modification level rather than genetic material impairment. We also found that ZDHHC5 mediates IFT81 palmitoylation, regulates IFT81 in round spermatids, and links to sperm tail malformations. These findings establish ZDHHC5, a palmitoyltransferase, as a pivotal regulator of spermatogenesis, thereby yielding new insights into the molecular mechanisms underlying male infertility.
Study Information
pubmed
2025
2025-11-03T00:00:00.000Z
10.1530/rep-25-0310