Almacenamiento post-descongelación de esperma como herramienta para revelar genes asociados a efectos paternos en la...

The influence of paternity on progeny quality, particularly during early developmental stages, has long been underappreciated. However, altered sperm phenotypes are increasingly recognized as effective tools for identifying paternal-effect-associated genes (PEAGs), whose expression in the progeny is influenced by genetic or non-genetic factors carried by the sperm. This study investigated the impact of post-thaw sperm storage (PTS) as a stressor to verify its effect on larval performance in common garden rearing trial and to reveal PEAGs in Eurasian perch (Perca fluviatilis) progeny. In vitro fertilizations were performed using cryopreserved sperm that was either used immediately after thawing (0 min; CON) or after 30 min of post-thaw storage at 4 °C.

Despite a marked decline in sperm motility during PTS, fertilization success remained unaffected, allowing the use of PTS to study its effect on progeny phenotype. Notably, larvae from the PTS group exhibited significantly higher mortality starting from 9 days post hatch, indicating strong paternal influences on early larval viability. Transcriptomic profiling of larvae at the mouth-opening stage, selected to minimize rearing-induced variation, identified 41 differentially expressed genes (DEGs), many linked to immune regulatory pathways. This suggests that paternal inputs may shape larval immune function, potentially contributing to observed mortality differences. Among the DEGs, several genes, mfap4, gimap, hlag, pigr, neo1, and pde6g, emerged as strong candidate PEAGs.

This study shows that even a brief, 30-minute PTS not only reduces sperm motility but also imprints lasting effects on progeny performance and survival. By selectively shaping the pool of functional sperm, PTS acts as an additional layer of selection, enriching for cells with specific traits and offering a powerful, controlled system for studying non-genetic inheritance factors and identifying PEAGs in fish. Transcriptomic analysis uncovered a deeper dimension to this process, revealing that maternal identity can amplify or buffer paternal contributions which serves as evidence of a complex parental interplay that influences early development. In effect, this study provides a robust experimental model based on controlled, paired fertilization design together with transcriptomic profiling of the offspring to identify novel PEAGs and reveal molecular consequences of paternal variation induced by post-thaw storage.