Increasing methylation of sperm rDNA and other repetitive elements in the aging male mammalian germline. Issue 8 (1st July 2020)

• Record Type: Journal Article
• Authors: Potabattula, Ramya; Zacchini, Federica; Ptak, Grazyna Ewa; Dittrich, Marcus; Müller, Tobias; El Hajj, Nady; Hahn, Thomas; Drummer, Charis; Behr, Rüdiger; Lucas‐Hahn, Andrea; Niemann, Heiner; Schorsch, Martin; Haaf, Thomas
• Is Part Of: Aging cell. Volume 19:Issue 8(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-07-01
• Subjects: embryo developmental potential -- epigenetic clock -- germline aging -- repetitive DNA elements -- ribosomal DNA -- sperm DNA methylation; Cells -- Aging -- Periodicals; 571.8783605
• DOI: 10.1111/acel.13181
• Languages: English
• ISSNs: 1474-9718

Abstract

Abstract: In somatic cells/tissues, methylation of ribosomal DNA (rDNA) increases with age and age‐related pathologies, which has a direct impact on the regulation of nucleolar activity and cellular metabolism. Here, we used bisulfite pyrosequencing and show that methylation of the rDNA transcription unit including upstream control element (UCE), core promoter, 18S rDNA, and 28S rDNA in human sperm also significantly increases with donor's age. This positive correlation between sperm rDNA methylation and biological age is evolutionarily conserved among mammals with widely different life spans such as humans, marmoset, bovine, and mouse. Similar to the tandemly repeated rDNA, methylation of human α‐satellite and interspersed LINE1 repeats, marmoset α‐satellite, bovine alpha‐ and testis satellite I, mouse minor and major satellite, and LINE1‐T repeats increases in the aging male germline, probably related to their sperm histone packaging. Deep bisulfite sequencing of single rDNA molecules in human sperm revealed that methylation does not only depend on donor's age, but also depend on the region and sequence context (A vs. G alleles). Both average rDNA methylation of all analyzed DNA molecules and the number of fully (>50%) methylated alleles, which are thought to be epigenetically silenced, increase with donor's age. All analyzed CpGs in the sperm rDNA transcription unit show comparable age‐related methylation changes. Unlike other epigenetic aging markers, the rDNA clock appears to operate in similar ways in germline and soma in different mammalian species. We propose that sperm rDNA methylation, directly or indirectly, influences nucleolar formation and developmental potential in the early embryo. Abstract : Sperm methylation of the rDNA transcription unit increases with donor's age in mammals with widely different life spans. Scatter plots show positive correlations between donor's age ( x ‐axis in percentage of life span) and mean methylation ( y ‐axis in %) of 18S rDNA in 80 mouse (purple dots), 36 bull (yellow), 16 marmoset (red), and 295 human (green) sperm samples. An orthologous region covering 8 CpGs was analyzed by bisulfite pyrosequencing. The black regression line applies to all 427 analyzed samples.