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Mitochondrial DNA (mtDNA) mutagenesis remains poorly understood despite its crucial role in disease, aging, and evolutionary tracing. In this study, we reconstructed a comprehensive 192-component mtDNA mutational spectrum for chordates by analyzing 118,397 synonymous mutations in the CytB gene across 1,697 species and five classes. This analysis revealed three primary forces shaping mtDNA mutagenesis: (i) symmetrical, replication-driven errors by mitochondrial polymerase (POLG), resulting in C > T and A > G mutations that are highly conserved across classes; (ii) asymmetrical, damage-driven C > T mutations on the single-stranded heavy strand with clock-like dynamics; and (iii) asymmetrical A > G mutations on the heavy strand, with dynamics suggesting sensitivity to oxidative damage. The third component, sensitive to oxidative damage, positions mtDNA mutagenesis as a promising marker for metabolic and physiological processes across various classes, species, organisms, tissues, and cells. The deconvolution of the mutational spectra into mutational signatures uncovered deficiencies in both base excision repair (BER) and mismatch repair (MMR) pathways. Further analysis of mutation hotspots, abasic sites, and mutational asymmetries underscores the critical role of single-stranded DNA damage (components ii and iii), which, uncorrected due to BER and MMR deficiencies, contributes roughly as many mutations as POLG-induced errors (component i).
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http://dx.doi.org/10.1093/molbev/msae261 | DOI Listing |
Adv Exp Med Biol
August 2025
Department of Agricultural, Food, and Nutritional Science, University of Alberta, Edmonton, AB, Canada.
This chapter describes a molecular basis for age-induced muscle fiber loss involving the mammalian mitochondrial genome (mtDNA). Early studies of human mitochondrial myopathies, which display many phenotypes associated with muscle aging, led to the search for and subsequent discovery of similar genetic and histopathological changes in aging skeletal muscle. A diverse spectrum of mtDNA deletion mutations increase in abundance with age and clonally accumulate to high abundance within individual cells.
View Article and Find Full Text PDFInt J Mol Sci
July 2025
Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, CA 90027, USA.
Mitochondria are critical for cellular energy, and while large deletions in their genome (mtDNA) are linked to primary mitochondrial diseases, their significance in cancer is less understood. Given cancer's metabolic nature, investigating mtDNA deletions in tumors at various stages could provide insights into disease origins and treatment responses. In this study, we analyzed 148 bone marrow samples from 129 pediatric patients with B-cell (B-ALL) and T-cell (T-ALL) acute lymphoblastic leukemia at diagnosis, remission, and relapse using long-range PCR, next-generation sequencing, and the Splice-Break2 pipeline.
View Article and Find Full Text PDFInt J Mol Sci
July 2025
Department of Biology and Biotechnologies "C. Darwin", Sapienza University of Rome, 00185 Rome, Italy.
In this study, we investigated the mitochondrial defects resulting from the deletion of , a lysine-acetyltransferase, in the yeast . Gcn5 serves as the catalytic subunit of the SAGA acetylation complex and functions as an epigenetic regulator, primarily acetylating N-terminal lysine residues on histones H2B and H3 to modulate gene expression. The loss of leads to mitochondrial abnormalities, including defects in mitochondrial morphology, a reduced mitochondrial DNA copy number, and defective mitochondrial inheritance due to the depolarization of actin filaments.
View Article and Find Full Text PDFCureus
June 2025
Radiology, Bolan Medical Complex Hospital, Quetta, PAK.
Aging also contributes to cancer risk factor potentiation by disturbed iron metabolism and genomic instability, both of which contribute to enhanced risk of cancer, particularly in transfusion-dependent groups such as patients with β-thalassemia or myelodysplastic syndromes. Systemic iron overload results from chronic transfusions and progressively disturbed iron homeostasis and clonal hematopoiesis of indeterminate potential (CHIP) that contribute to oncogenic burden. All these create a permissive profile in which carcinogenesis is favored by oxidative stress, mitochondrial dysfunctions, immune suppression, and disrupted DNA repair.
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