Increased Paternal Age at Conception Is Associated with Transcriptomic Changes Involved in Mitochondrial Function in Elderly Individuals

• Published in: PloS one Vol. 11; no. 11; p. e0167028
• Main Authors: Nevalainen, Tapio, Kananen, Laura, Marttila, Saara, Jylhävä, Juulia, Jylhä, Marja, Hervonen, Antti, Hurme, Mikko
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 23.11.2016; Public Library of Science (PLoS)
• Subjects: Age; Aged, 80 and over; Aging - physiology; Autism; Biology and Life Sciences; Chemical energy; Conception (Human reproduction); Deoxyribonucleic acid; DNA; DNA biosynthesis; DNA methylation; DNA repair; Electron transport; Electron Transport - physiology; Female; Gene expression; Gene Expression Profiling; Gene Expression Regulation - physiology; Genetic aspects; Geriatrics; Germ cells; Health aspects; Health risk assessment; Humans; Leukocytes (mononuclear); Male; Male menopause; Medicine and Health Sciences; Mental disorders; Mitochondria; Mitochondria - metabolism; Mitochondrial diseases; Mitochondrial Proteins - biosynthesis; Mutation; Neurodevelopmental disorders; Nonagenarian; Offspring; Older people; Oogonia; Oxidative Phosphorylation; Oxidative stress; Peripheral blood mononuclear cells; Phosphorylation; Population studies; Replication; Research and analysis methods; Schizophrenia; Spermatogonia; Systematic review; Transcriptome - physiology; Translation termination; Finland
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0167028

The increased paternal age at conception (PAC) has been associated with autism spectrum disorder (ASD), schizophrenia and other neurodevelopmental disorders, thus raising questions that imply, potential health concerns in the offspring. As opposed to female oogonia, the male germ cells undergo hundreds of cell divisions during the fertile years. Thus, the advanced paternal age is associated with increase of point mutations in the male spermatogonia DNA, implying that this could be the major driving mechanism behind the paternal age effect observed in the offspring. In addition to replication errors, DNA replication fidelity and inefficient DNA repair machinery in the spermatogonia also contribute to the mutagenic load. Our study population consisted of 38 nonagenarians, participants in the Vitality 90+ Study, born in the year 1920 (women n = 25, men n = 13), for whom the parental birth dates were available. The gene expression profile of the study subjects was determined with HumanHT-12 v4 Expression BeadChip from peripheral blood mononuclear cells. We used Spearman's rank correlation to look for the associations of gene expression with paternal age at conception. Associated transcripts were further analyzed with GOrilla and IPA to determine enriched cellular processes and pathways. PAC was associated with the expression levels of 648 transcripts in nonagenarian subjects. These transcripts belonged to the process of mitochondrial translational termination and the canonical pathway of Mitochondrial dysfunction, more specifically of Oxidative phosphorylation. The observed systematic down-regulation of several mitochondrial respiratory chain components implies compromised function in oxidative phosphorylation and thus in the production of chemical energy.