Aging Dads’ Impact: Age-Altered Sperm Genetics Increase Autism Risk – Neuroscience News

Summary: A study reveals that aging in male mice leads to changes in sperm microRNAs (miRNAs) that could influence offspring development. The research team conducted a detailed analysis of sperm from young and older mice, uncovering significant age-related alterations in miRNAs, some of which regulate the nervous system and genes linked to autism spectrum disorder. These findings highlight the growing understanding of paternal age’s impact on offspring, particularly in the context of neurodevelopmental disorders. This study emphasizes the importance of considering paternal factors in reproductive health and disease prevention for future generations. Key Facts: The study identified significant age-related changes in sperm microRNAs in mice, which could be transferred to fertilized eggs and impact offspring development. Altered microRNAs were found to regulate genes related to the nervous system and autism spectrum disorder. This research contributes to a broader understanding of how paternal aging can influence the health and development of offspring, especially regarding neurodevelopmental disorders. Source: Tohoku University A recent study has reported that changes in mice sperm microRNAs brought about by aging may affect the growth and development of offspring. The finding adds to the growing literature on the effects of paternal aging on offspring. Details of the study were published in the journal  Scientific Reports  on December 7, 2023. Marriages and childbearing later in life are increasingly becoming the norm. While the impacts of maternal age on offspring, such as a higher risk of miscarriage and Down syndrome, are widely understood, the impacts from the paternal side are less so. Yet this is changing. Recent epidemiological studies have demonstrated that paternal aging exerts a more substantial influence on the heightened risk of neurodevelopmental disorders such as autism spectrum disorder. A research team led by Professor Noriko Osumi from the Department of Developmental Neuroscience at the Tohoku University Graduate School of Medicine has previously revealed that epigenetic factors, including histone modifications in spermatogenesis and DNA methylation in mice sperm, undergo changes with age. These alterations might lead to transgenerational effects. However, the impact of paternal aging on microRNAs (miRNAs), small, non-coding RNA molecules that play a crucial role in regulating gene expression, remains under-explored. To rectify this, the same research team has conducted a comprehensive analysis of age-related variations in microRNAs in mice sperm. They compared microRNAs in sperm from mice aged 3, 12, and 20 months and identified the microRNAs that had changed in quantity. The researchers discovered significant age-associated differences in the microRNAs. Some changes were in microRNAs responsible for regulating the nervous system and genes related to autism spectrum disorder, and these altered microRNAs included those transferred to fertilized eggs. “Our study reveals the potential association between alteration in sperm microRNAs caused by paternal aging, underscoring the significance of investigating the impact of sperm microRNAs on offspring, an aspect that has been relatively overlooked in previous research,” states Osumi. The anticipation is that further exploration of epigenetic factors, specifically microRNAs, will not only contribute to unraveling the pathogenic mechanisms underlying neurodevelopmental disorders but will also offer insights into promoting the health and disease prevention of successive generations. Osumi points out that their study widens the net when it comes to exploring the link between paternal age and potential health complications in children. “While the age-related changes in oocytes are well-documented, the focus has predominantly centered on the fertility of sperm. Recognizing the myriad epigenetic transformations associated with sperm aging, as exemplified by the microRNAs examined in this study, becomes imperative.” The findings also gain relevance in the context of Japan’s rapidly declining birthrate, which necessitates incorporating the perspective on sperm-related factors in advancing reproductive medicine. About this aging, genetics, and neurodevelopment research news Author: Noriko Osumi Source: Tohoku University Contact: Noriko Osumi – Tohoku University Image: The image is credited to Neuroscience News Original Research: Open access. “Investigating the impact of paternal aging on murine sperm miRNA profiles and their potential link to autism spectrum disorder” by Noriko Osumi et al. Scientific Reports Abstract Investigating the impact of paternal aging on murine sperm miRNA profiles and their potential link to autism spectrum disorder Paternal aging has consistently been linked to an increased risk of neurodevelopmental disorders, including autism spectrum disorder (ASD), in offspring. Recent evidence has highlighted the involvement of epigenetic factors. In this study, we aimed to investigate age-related alterations in microRNA (miRNA) profiles of mouse sperm and analyze target genes regulated by differentially expressed miRNAs (DEmiRNAs). Microarray analyses were conducted on sperm samples from mice at different ages: 3 months (3 M), over 12 M, and beyond 20 M. We identified 26 miRNAs with differential expression between the 3 and 20 M mice, 34 miRNAs between the 12 and 20 M mice, and 2 miRNAs between the 3 and 12 M mice. The target genes regulated by these miRNAs were significantly associated with apoptosis/ferroptosis pathways and the nervous system. We revealed alterations in sperm miRNA profiles due to aging and suggest that the target genes regulated by these DEmiRNAs are associated with apoptosis and the nervous system, implying a potential link between paternal aging and an increased risk of neurodevelopmental disorders such as ASD. The observed age-related changes in sperm miRNA profiles have the potential to impact sperm quality and subsequently affect offspring development.

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