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No evidence of extensive non-CpG methylation in mtDNA.
Guitton, Romain; Nido, Gonzalo S; Tzoulis, Charalampos.
Afiliação
  • Guitton R; Neuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
  • Nido GS; Department of Clinical Medicine, University of Bergen, Pb 7804, 5020 Bergen, Norway.
  • Tzoulis C; Neuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
Nucleic Acids Res ; 50(16): 9190-9194, 2022 09 09.
Article em En | MEDLINE | ID: mdl-35979955
While most research suggests mitochondrial DNA (mtDNA) harbors low or no methylation, a few studies claim to report evidence of high-level methylation in the mtDNA. The reasons behind these contradictory results are likely to be methodological but remain largely unexplored. Here, we critically reanalyzed a recent study by Patil et al. (2019) reporting extensive methylation in human mtDNA in a non-CpG context. Our analyses refute the original findings and show that these do not reflect the biology of the tested samples, but rather stem from a combination of methodological and technical pitfalls. The authors employ an oversimplified model that defines as methylated all reference positions with methylation proportions above an arbitrary cutoff of 9%. This substantially exacerbates the overestimation of methylated cytosines due to the selective degradation of unmethylated cytosine-rich regions. Additional limitations are the small sample sizes and lack of sample-specific controls for bisulfite conversion efficiency. In conclusion, using the same dataset employed in the original study by Patil et al., we find no evidence supporting the existence of extensive non-CpG methylation in the human mtDNA.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Metilação de DNA Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nucleic Acids Res Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Noruega País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Metilação de DNA Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nucleic Acids Res Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Noruega País de publicação: Reino Unido