Genome-wide characterization of mitochondrial DNA methylation in human brain

• Published in: Frontiers in endocrinology (Lausanne) Vol. 13; p. 1059120
• Main Authors: Devall, Matthew, Soanes, Darren M, Smith, Adam R, Dempster, Emma L, Smith, Rebecca G, Burrage, Joe, Iatrou, Artemis, Hannon, Eilis, Troakes, Claire, Moore, Karen, O'Neill, Paul, Al-Sarraj, Safa, Schalkwyk, Leonard, Mill, Jonathan, Weedon, Michael, Lunnon, Katie
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 16.01.2023
• Subjects: 5-Methylcytosine (5mC); Brain; DNA Methylation; DNA, Mitochondrial - genetics; DNA, Mitochondrial - metabolism; Endocrinology; epigenetics; Genes, Mitochondrial; Humans; Mitochondria; Mitochondria - genetics; Mitochondria - metabolism; mtDNA; Brain; 5-Methylcytosine (5mC); DNA Methylation; Mitochondria; mtDNA; epigenetics
• ISSN: 1664-2392; 1664-2392
• DOI: 10.3389/fendo.2022.1059120

There is growing interest in the role of DNA methylation in regulating the transcription of mitochondrial genes, particularly in brain disorders characterized by mitochondrial dysfunction. Here, we present a novel approach to interrogate the mitochondrial DNA methylome at single base resolution using targeted bisulfite sequencing. We applied this method to investigate mitochondrial DNA methylation patterns in post-mortem superior temporal gyrus and cerebellum brain tissue from seven human donors. We show that mitochondrial DNA methylation patterns are relatively low but conserved, with peaks in DNA methylation at several sites, such as within the and the genes , , , and , predominantly in a non-CpG context. The elevated DNA methylation we observe in the we validate using pyrosequencing. We identify loci that show differential DNA methylation patterns associated with age, sex and brain region. Finally, we replicate previously reported differentially methylated regions between brain regions from a methylated DNA immunoprecipitation sequencing study. We have annotated patterns of DNA methylation at single base resolution across the mitochondrial genome in human brain samples. Looking to the future this approach could be utilized to investigate the role of mitochondrial epigenetic mechanisms in disorders that display mitochondrial dysfunction.