A>G substitutions on a heavy chain of mitochondrial genome marks an increased level of aerobic metabolism in warm versus cold vertebrates

The variation in the mutational spectrum of the mitochondrial genome (mtDNA) among species is not well understood. Recently, we demonstrated an increase in A>G substitutions on a heavy chain (hereafter AH>GH) of mtDNA in aged mammals, interpreting it as a hallmark of age-related oxidative damage. In this study, we hypothesized that the occurrence of AH>GH substitutions may depend on the level of aerobic metabolism, which can be inferred from an organism’s body temperature. To test this hypothesis, we used body temperature in endotherms and environmental temperature in ectotherms as proxies for metabolic rate and reconstructed mtDNA mutational spectra for 1350 vertebrate species. Our results showed that temperature was associated with increased rates of AH>GH and asymmetry of AH>GH in different species of ray-finned fishes and within geographically distinct clades of European anchovy. Analysis of nucleotide composition in the most neutral synonymous sites of fishes revealed that warm-water species were expectedly more A-poor and G-rich compared to cold-water species. Finally, we extended our analyses to all vertebrates and observed higher AH>GH and increased asymmetry of AH>GH in warm-blooded (mammals and birds) compared to cold-blooded (Actinopterygii, amphibia, reptilia) vertebrate classes. Overall, our findings suggest that temperature, through its influence on metabolism and oxidative damage, shapes the mutational properties and nucleotide content of the mtDNA in all vertebrates.

[1]  M. Pfenninger,et al.  Temperature-dependence of spontaneous mutation rates , 2020, bioRxiv.

[2]  Marzia A. Cremona,et al.  Age-related accumulation of de novo mitochondrial mutations in mammalian oocytes and somatic tissues , 2020, PLoS biology.

[3]  A. Reymond,et al.  Mammalian mitochondrial mutational spectrum as a hallmark of cellular and organismal aging , 2019, bioRxiv.

[4]  Martin J. Aryee,et al.  Lineage Tracing in Humans Enabled by Mitochondrial Mutations and Single-Cell Genomics , 2019, Cell.

[5]  Kui Lin,et al.  Temperature responses of mutation rate and mutational spectrum in an Escherichia coli strain and the correlation with metabolic rate , 2018, BMC Evolutionary Biology.

[6]  João Pedro de Magalhães,et al.  Human Ageing Genomic Resources: new and updated databases , 2017, Nucleic Acids Res..

[7]  Nuno A. Fonseca,et al.  Comprehensive molecular characterization of mitochondrial genomes in human cancers , 2017, bioRxiv.

[8]  P. Rainey,et al.  Anaerobically Grown Escherichia coli Has an Enhanced Mutation Rate and Distinct Mutational Spectra , 2017, PLoS genetics.

[9]  J. de Magalhães,et al.  Being cool: how body temperature influences ageing and longevity , 2015, Biogerontology.

[10]  P. Martel,et al.  Thermal adaptation and clinal mitochondrial DNA variation of European anchovy , 2014, Proceedings of the Royal Society B: Biological Sciences.

[11]  Bin Tean Teh,et al.  Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer , 2014, eLife.

[12]  C. Baer,et al.  Temperature, stress and spontaneous mutation in Caenorhabditis briggsae and Caenorhabditis elegans , 2013, Biology Letters.

[13]  N. Galtier,et al.  Strong variations of mitochondrial mutation rate across mammals--the longevity hypothesis. , 2007, Molecular biology and evolution.

[14]  Harold R Lee,et al.  Fidelity of the Human Mitochondrial DNA Polymerase* , 2006, Journal of Biological Chemistry.

[15]  A. Eyre-Walker,et al.  An investigation of the variation in the transition bias among various animal mitochondrial DNA. , 2005, Gene.

[16]  James H. Brown,et al.  The rate of DNA evolution: effects of body size and temperature on the molecular clock. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[17]  Jeremiah J Faith,et al.  Likelihood analysis of asymmetrical mutation bias gradients in vertebrate mitochondrial genomes. , 2003, Genetics.

[18]  M. Turker,et al.  A:T --> G:C base pair substitutions occur at a higher rate than other substitution events in Pms2 deficient mouse cells. , 2002, DNA repair.

[19]  James H. Brown,et al.  UNM Digital Repository UNM Digital Repository Effects of size and temperature on metabolic rate Effects of size and temperature on metabolic rate , 2022 .

[20]  Andrew P. Martin,et al.  Body size, metabolic rate, generation time, and the molecular clock. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[21]  N. Timoféeff-ressovsky Qualitativer Vergleich der Mutabilität vonDrosophila funebris undDrosophila melanogaster , 1936, Zeitschrift für Induktive Abstammungs- und Vererbungslehre.

[22]  H. Coller,et al.  Origins of human mitochondrial point mutations as DNA polymerase gamma-mediated errors. , 2006, Mutation research.

[23]  D. Lindgren The temperature influence on the spontaneous mutation rate. I. Literature review. , 1972, Hereditas.