Mitochondrial metabolism and DNA methylation: a review of the interaction between two genomes

A FC Lopes - Clinical Epigenetics, 2020 - Springer
Mitochondria are controlled by the coordination of two genomes: the mitochondrial and the
nuclear DNA. As such, variations in nuclear gene expression as a consequence of …

The role of mitochondria in rheumatic diseases

YLC Becker, B Duvvuri, PR Fortin, C Lood… - Nature Reviews …, 2022 - nature.com
The mitochondrion is an intracellular organelle thought to originate from endosymbiosis
between an ancestral eukaryotic cell and an α-proteobacterium. Mitochondria are the …

An atlas of mitochondrial DNA genotype–phenotype associations in the UK Biobank

E Yonova-Doing, C Calabrese, A Gomez-Duran… - Nature …, 2021 - nature.com
Mitochondrial DNA (mtDNA) variation in common diseases has been underexplored, partly
due to a lack of genotype calling and quality-control procedures. Developing an at-scale …

Mitochondrial neurodegeneration

M Zeviani, C Viscomi - Cells, 2022 - mdpi.com
Mitochondria are cytoplasmic organelles, which generate energy as heat and ATP, the
universal energy currency of the cell. This process is carried out by coupling electron …

The role of mitochondria in human fertility and early embryo development: what can we learn for clinical application of assessing and improving mitochondrial DNA?

A Podolak, I Woclawek-Potocka, K Lukaszuk - Cells, 2022 - mdpi.com
Mitochondria are well known as 'the powerhouses of the cell'. Indeed, their major role is
cellular energy production driven by both mitochondrial and nuclear DNA. Such a feature …

Inheritance of mitochondrial DNA in humans: implications for rare and common diseases

W Wei, PF Chinnery - Journal of internal medicine, 2020 - Wiley Online Library
The first draft human mitochondrial DNA (mtDNA) sequence was published in 1981, paving
the way for two decades of discovery linking mtDNA variation with human disease. Severe …

Deciphering the genetic and epidemiological landscape of mitochondrial DNA abundance

S Hägg, J Jylhävä, Y Wang, K Czene, F Grassmann - Human Genetics, 2021 - Springer
Mitochondrial (MT) dysfunction is a hallmark of aging and has been associated with most
aging-related diseases as well as immunological processes. However, little is known about …

Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases

N Cai, A Gomez-Duran, E Yonova-Doing, K Kundu… - Nature medicine, 2021 - nature.com
Mitochondrial DNA (mtDNA) variants influence the risk of late-onset human diseases, but the
reasons for this are poorly understood. Undertaking a hypothesis-free analysis of 5,689 …

Mitoepigenetics and its emerging roles in cancer

Z Dong, L Pu, H Cui - Frontiers in cell and developmental biology, 2020 - frontiersin.org
In human beings, there is a∼ 16,569 bp circular mitochondrial DNA (mtDNA) encoding 22
tRNAs, 12S and 16S rRNAs, 13 polypeptides that constitute the central core of ETC/OxPhos …

[HTML][HTML] Current and new next-generation sequencing approaches to study mitochondrial DNA

A Legati, N Zanetti, A Nasca, C Peron… - The Journal of Molecular …, 2021 - Elsevier
Mitochondria harbor multiple copies of a maternally inherited nonnuclear genome. Point
mutations, deletions, or depletion of the mitochondrial DNA (mtDNA) are associated with …