Towards a kingdom of reproductive life - the core sperm proteome

• Published in: Reproduction (Cambridge, England) Vol. 169; no. 6
• Main Authors: Pini, Taylor, Nixon, Brett, Karr, Timothy L, Teperino, Raffaele, Sanz-Moreno, Adrián, da Silva-Buttkus, Patricia, Tüttelmann, Frank, Kliesch, Sabine, Gailus-Durner, Valérie, Fuchs, Helmut, Marschall, Susan, Hrabě de Angelis, Martin, Skerrett-Byrne, David A
• Format: Journal Article
• Language: English
• Published: England Bioscientifica Ltd 01.06.2025
• Subjects: Animals; Female; Fertilization - physiology; Humans; Male; Mice; Proteome - metabolism; Proteomics - methods; Reproduction - physiology; Sperm Motility - physiology; Spermatozoa - metabolism; Echs1; Ndufa10; proteomics; Pebp4; bioinformatics; fertility; Aldh7a1; Etfb; sperm; data reanalysis; sperm proteome
• ISSN: 1470-1626; 1741-7899; 1741-7899
• DOI: 10.1530/REP-25-0105

Sperm function is essential for fertility across humans, agriculture and wildlife, yet comparative studies remain limited. This study integrates multi-species proteomic data to identify a core sperm proteome, uncovering conserved molecular pathways and validating novel sperm proteins critical for motility and fertilization. Reproductive biology is often considered in three siloed research areas; humans, agriculture and wildlife. Yet, each demand solutions for treatment of subfertility, fertility biomarkers, development of assisted reproductive technologies and effective contraception. To efficiently develop solutions applicable to all species, we must improve our understanding of the common biology underpinning reproductive processes. Accordingly, we integrate proteomic data from 29 publicly available datasets (>2 TB of data) to characterize mature sperm proteomes spanning 12 vertebrate species, identifying 13,853 proteins. Although human and mouse have relatively well-annotated sperm proteomes, many non-model species rely heavily on predicted or homology-inferred identifications. Despite variation in proteome size, composition and reproductive strategies, comparative analyses revealed that vertebrates share a fundamental molecular framework essential for sperm function. A core set of 45 species-level and 135 order-level conserved proteins mapped to critical processes, including energy generation, acrosome function and novel signalling pathways (BAG2 and FAT10). Knockout mouse models further validate the significance of these conserved proteins, demonstrating that their disruption impairs sperm motility and fertilization capacity. Moreover, we discovered loss-of-function variants of two additional core sperm proteins in clinical samples, linking them to severe sperm defects. Intriguingly, in-silico analysis reveals function-driven, context-dependent diversity surpassing evolutionary patterns. Collectively, these results highlight the value of integrating publicly available datasets and underscore the need for improved genome/proteome annotation in non-model species in mammals. This work provides a foundation for developing cross-species strategies to enhance fertility treatments, assisted reproductive technologies and conservation efforts. All data are available via ShinySpermKingdom (https://reproproteomics.shinyapps.io/ShinySpermKingdom/).