Sperm sncRNA networks are synchronized by a coordination between adverse childhood experiences (ACE) and current stress

While stress in the environment alters sperm function and fertility, the underlying biology is not understood. Our prior studies showed that current stress could significantly change the composition and levels of sperm small noncoding (sncRNA) and impact sperm motility in men. However, the additional influence of adversity experienced earlier in life, designated as adverse childhood experiences (ACE), on sperm sncRNA dynamics remains unclear. To expand our understanding of the important relationship between ACE and stress, we recruited a longitudinal human cohort and modeled differential sncRNA and co-expression networks associated with perceived stress and ACE. Utilizing a repeated measures design, we were able to identify significant time-dependent interactions between ACE and perceived stress that resulted in differential sncRNA expression. Furthermore, network analyses revealed ACE and perceived stress coordinated sncRNA across subtypes, including miRNA that target genes important for offspring development. As these changes were identified widely across sncRNA subtypes, our findings reflect a novel and exciting synchronization strategy by which current and past experiences can impact the next generation. Evolutionarily, this coordination would preserve sncRNA modules essential for species survival while allowing refinement around developmental pathways important for intergenerational fitness.

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Publication Details

Journal
Scientific Reports
Published
2026-04-17
DOI
https://doi.org/10.1038/s41598-026-47542-2
Primary Topic
Sperm and Testicular Function
Type
article
Field-Weighted Citation Impact
0.00

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article

Sperm sncRNA networks are synchronized by a coordination between adverse childhood experiences (ACE) and current stress

Mary D. Sammel, Tracy L. Bale, Sergio N. Simões, C. Neill Epperson et al.
Scientific Reports
Sperm and Testicular Function
article

Sperm sncRNA networks are synchronized by a coordination between adverse childhood experiences (ACE) and current stress

Mary D. Sammel, Tracy L. Bale, Sergio N. Simões, C. Neill Epperson, Helena Brentani, Nickole Moon, Rachel L. Johnson, Arthur S. Feltrin, David C. Martins-Jr, Caio Braga, Alyssa Jeng
article en

Abstract

While stress in the environment alters sperm function and fertility, the underlying biology is not understood. Our prior studies showed that current stress could significantly change the composition and levels of sperm small noncoding (sncRNA) and impact sperm motility in men. However, the additional influence of adversity experienced earlier in life, designated as adverse childhood experiences (ACE), on sperm sncRNA dynamics remains unclear. To expand our understanding of the important relationship between ACE and stress, we recruited a longitudinal human cohort and modeled differential sncRNA and co-expression networks associated with perceived stress and ACE. Utilizing a repeated measures design, we were able to identify significant time-dependent interactions between ACE and perceived stress that resulted in differential sncRNA expression. Furthermore, network analyses revealed ACE and perceived stress coordinated sncRNA across subtypes, including miRNA that target genes important for offspring development. As these changes were identified widely across sncRNA subtypes, our findings reflect a novel and exciting synchronization strategy by which current and past experiences can impact the next generation. Evolutionarily, this coordination would preserve sncRNA modules essential for species survival while allowing refinement around developmental pathways important for intergenerational fitness.

Scientific Reports
Colorado School of Public Health (US), Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (BR), Instituto Federal do Espírito Santo (BR), University of Colorado Anschutz Medical Campus (US), Universidade Federal do ABC (BR)
Fundação de Amparo à Pesquisa do Estado de São Paulo, National Institutes of Health, National Institute of Mental Health, National Institute of Child Health and Human Development
Life in Land
Openalex Percentile: Top 15%
Sperm and Testicular Function
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