Biology:Mitochondrial DNA

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Short description: DNA located in mitochondria
Mitochondrial DNA is the small circular chromosome found inside mitochondria. These organelles, found in all eukaryotic cells, are the powerhouse of the cell.[1] The mitochondria, and thus mitochondrial DNA, are passed exclusively from mother to offspring through the egg cell.

File:Mitochondrial DNA 3D.webm

Electron microscopy reveals mitochondrial DNA in discrete foci. Bars: 200 nm. (A) Cytoplasmic section after immunogold labelling with anti-DNA; gold particles marking mtDNA are found near the mitochondrial membrane (black dots in upper right). (B) Whole mount view of cytoplasm after extraction with CSK buffer and immunogold labelling with anti-DNA; mtDNA (marked by gold particles) resists extraction. From Iborra et al., 2004.[jargon][2]

Mitochondrial DNA (mtDNA or mDNA)[3] is the DNA located in mitochondria, cellular organelles within eukaryotic cells that convert chemical energy from food into a form that cells can use, such as adenosine triphosphate (ATP). Mitochondrial DNA is only a small portion of the DNA in a eukaryotic cell; most of the DNA can be found in the cell nucleus and, in plants and algae, also in plastids such as chloroplasts.

Human mitochondrial DNA was the first significant part of the human genome to be sequenced.[4] This sequencing revealed that the human mtDNA includes 16,569 base pairs and encodes 13 proteins.

Since animal mtDNA evolves faster than nuclear genetic markers,[5][6][7] it represents a mainstay of phylogenetics and evolutionary biology. It also permits tracing the relationships of populations, and so has become important in anthropology and biogeography.

Origin

Nuclear and mitochondrial DNA are thought to have separate evolutionary origins, with the mtDNA derived from the circular genomes of bacteria engulfed by the ancestors of modern eukaryotic cells. This theory is called the endosymbiotic theory. In the cells of extant organisms, the vast majority of the proteins in the mitochondria (numbering approximately 1500 different types in mammals) are coded by nuclear DNA, but the genes for some, if not most, of them are thought to be of bacterial origin, having been transferred to the eukaryotic nucleus during evolution.[8]

The reasons mitochondria have retained some genes are debated. The existence in some species of mitochondrion-derived organelles lacking a genome[9] suggests that complete gene loss is possible, and transferring mitochondrial genes to the nucleus has several advantages.[10] The difficulty of targeting remotely-produced hydrophobic protein products to the mitochondrion is one hypothesis for why some genes are retained in mtDNA;[11] colocalisation for redox regulation is another, citing the desirability of localised control over mitochondrial machinery.[12] Recent analysis of a wide range of mtDNA genomes suggests that both these features may dictate mitochondrial gene retention.[8]

Genome structure and diversity

Across all organisms, there are six main mitochondrial genome types, classified by structure (i.e. circular versus linear), size, presence of introns or plasmid like structures, and whether the genetic material is a singular molecule or collection of homogeneous or heterogeneous molecules.[13]

In many unicellular organisms (e.g., the ciliate Tetrahymena and the green alga Chlamydomonas reinhardtii), and in rare cases also in multicellular organisms (e.g. in some species of Cnidaria), the mtDNA is linear DNA. Most of these linear mtDNAs possess telomerase-independent telomeres (i.e., the ends of the linear DNA) with different modes of replication, which have made them interesting objects of research because many of these unicellular organisms with linear mtDNA are known pathogens.[14]

Animals

Most (bilaterian) animals have a circular mitochondrial genome. Medusozoa and calcarea clades however include species with linear mitochondrial chromosomes.[15] With a few exceptions, animals have 37 genes in their mitochondrial DNA: 13 for proteins, 22 for tRNAs, and 2 for rRNAs.[16]

Mitochondrial genomes for animals average about 16,000 base pairs in length.[16] The anemone Isarachnanthus nocturnus has the largest mitochondrial genome of any animal at 80,923 bp.[17] The smallest known mitochondrial genome in animals belongs to the comb jelly Vallicula multiformis, which consist of 9,961 bp.[18]

In February 2020, a jellyfish-related parasite – Henneguya salminicola – was discovered that lacks a mitochondrial genome but retains structures deemed mitochondrion-related organelles. Moreover, nuclear DNA genes involved in aerobic respiration and in mitochondrial DNA replication and transcription were either absent or present only as pseudogenes. This is the first multicellular organism known to have this absence of aerobic respiration and lives completely free of oxygen dependency.[19][20]

Plants and fungi

There are three different mitochondrial genome types in plants and fungi. The first type is a circular genome that has introns (type 2) and may range from 19 to 1000 kbp in length. The second genome type is a circular genome (about 20–1000 kbp) that also has a plasmid-like structure (1 kb) (type 3). The final genome type found in plants and fungi is a linear genome made up of homogeneous DNA molecules (type 5).[21][22][23]

Great variation in mtDNA gene content and size exists among fungi and plants, although there appears to be a core subset of genes present in all eukaryotes (except for the few that have no mitochondria at all).[8] In Fungi, however, there is no single gene shared among all mitogenomes.[24] Some plant species have enormous mitochondrial genomes, with Silene conica mtDNA containing as many as 11,300,000 base pairs.[25] Surprisingly, even those huge mtDNAs contain the same number and kinds of genes as related plants with much smaller mtDNAs.[26] The genome of the mitochondrion of the cucumber (Cucumis sativus) consists of three circular chromosomes (lengths 1556, 84 and 45 kilobases), which are entirely or largely autonomous with regard to their replication.[27]

Protists

Protists contain the most diverse mitochondrial genomes, with five different types found in this kingdom. Type 2, type 3 and type 5 of the plant and fungal genomes also exist in some protists, as do two unique genome types. One of these unique types is a heterogeneous collection of circular DNA molecules (type 4) while the other is a heterogeneous collection of linear molecules (type 6). Genome types 4 and 6 each range from 1–200 kbp in size.[citation needed]

The smallest mitochondrial genome sequenced to date is the 5,967 bp mtDNA of the parasite Plasmodium falciparum.[28][29]

Endosymbiotic gene transfer, the process by which genes that were coded in the mitochondrial genome are transferred to the cell's main genome, likely explains why more complex organisms such as humans have smaller mitochondrial genomes than simpler organisms such as protists.

Genome Type[13] Kingdom Introns Size Shape Description
1 Animal No 11–28 kbp Circular Single molecule
2 Fungi, Plant, Protista Yes 19–1000 kbp Circular Single molecule
3 Fungi, Plant, Protista No 20–1000 kbp Circular Large molecule and small plasmid like structures
4 Protista No 1–200 kbp Circular Heterogeneous group of molecules
5 Fungi, Plant, Protista No 1–200 kbp Linear Homogeneous group of molecules
6 Protista No 1–200 kbp Linear Heterogeneous group of molecules

Replication

Mitochondrial DNA is replicated by the DNA polymerase gamma complex which is composed of a 140 kDa catalytic DNA polymerase encoded by the POLG gene and two 55 kDa accessory subunits encoded by the POLG2 gene.[30] The replisome machinery is formed by DNA polymerase, TWINKLE and mitochondrial SSB proteins. TWINKLE is a helicase, which unwinds short stretches of dsDNA in the 5' to 3' direction.[31] All these polypeptides are encoded in the nuclear genome.

During embryogenesis, replication of mtDNA is strictly down-regulated from the fertilized oocyte through the preimplantation embryo.[32] The resulting reduction in per-cell copy number of mtDNA plays a role in the mitochondrial bottleneck, exploiting cell-to-cell variability to ameliorate the inheritance of damaging mutations.[33] According to Justin St. John and colleagues, "At the blastocyst stage, the onset of mtDNA replication is specific to the cells of the trophectoderm.[32] In contrast, the cells of the inner cell mass restrict mtDNA replication until they receive the signals to differentiate to specific cell types."[32]

Human mitochondrial DNA with the 37 genes on their respective H- and L-strands

Genes on the human mtDNA and their transcription

Further information: Biology:Human mitochondrial genetics
Schematic karyogram showing the human genome, with 23 chromosome pairs as well as the mitochondrial genome (to scale at bottom left, annotated "MT"). Its genome is relatively tiny compared to the rest, and its copy number per human cell varies from 0 (erythrocytes)[34] up to 1,500,000 (oocytes).[35]
Further information: Karyotype

The two strands of the human mitochondrial DNA are distinguished as the heavy strand and the light strand. The heavy strand is rich in guanine and encodes 12 subunits of the oxidative phosphorylation system, two ribosomal RNAs (12S and 16S), and 14 transfer RNAs (tRNAs). The light strand encodes one subunit, and 8 tRNAs. So, altogether mtDNA encodes for two rRNAs, 22 tRNAs, and 13 protein subunits, all of which are involved in the oxidative phosphorylation process.[36][37]

The 37 genes of the Cambridge Reference Sequence for human mitochondrial DNA and their locations[38]
Gene Type Product Positions
in the mitogenome 		Strand
MT-ATP8 protein coding ATP synthase, Fo subunit 8 (complex V) 08,366–08,572 (overlap with MT-ATP6) H
MT-ATP6 protein coding ATP synthase, Fo subunit 6 (complex V) 08,527–09,207 (overlap with MT-ATP8) H
MT-CO1 protein coding Cytochrome c oxidase, subunit 1 (complex IV) 05,904–07,445 H
MT-CO2 protein coding Cytochrome c oxidase, subunit 2 (complex IV) 07,586–08,269 H
MT-CO3 protein coding Cytochrome c oxidase, subunit 3 (complex IV) 09,207–09,990 H
MT-CYB protein coding Cytochrome b (complex III) 14,747–15,887 H
MT-ND1 protein coding NADH dehydrogenase, subunit 1 (complex I) 03,307–04,262 H
MT-ND2 protein coding NADH dehydrogenase, subunit 2 (complex I) 04,470–05,511 H
MT-ND3 protein coding NADH dehydrogenase, subunit 3 (complex I) 10,059–10,404 H
MT-ND4L protein coding NADH dehydrogenase, subunit 4L (complex I) 10,470–10,766 (overlap with MT-ND4) H
MT-ND4 protein coding NADH dehydrogenase, subunit 4 (complex I) 10,760–12,137 (overlap with MT-ND4L) H
MT-ND5 protein coding NADH dehydrogenase, subunit 5 (complex I) 12,337–14,148 H
MT-ND6 protein coding NADH dehydrogenase, subunit 6 (complex I) 14,149–14,673 L
MT-RNR2 protein coding Humanin — —
MT-TA transfer RNA tRNA-Alanine (Ala or A) 05,587–05,655 L
MT-TR transfer RNA tRNA-Arginine (Arg or R) 10,405–10,469 H
MT-TN transfer RNA tRNA-Asparagine (Asn or N) 05,657–05,729 L
MT-TD transfer RNA tRNA-Aspartic acid (Asp or D) 07,518–07,585 H
MT-TC transfer RNA tRNA-Cysteine (Cys or C) 05,761–05,826 L
MT-TE transfer RNA tRNA-Glutamic acid (Glu or E) 14,674–14,742 L
MT-TQ transfer RNA tRNA-Glutamine (Gln or Q) 04,329–04,400 L
MT-TG transfer RNA tRNA-Glycine (Gly or G) 09,991–10,058 H
MT-TH transfer RNA tRNA-Histidine (His or H) 12,138–12,206 H
MT-TI transfer RNA tRNA-Isoleucine (Ile or I) 04,263–04,331 H
MT-TL1 transfer RNA tRNA-Leucine (Leu-UUR or L) 03,230–03,304 H
MT-TL2 transfer RNA tRNA-Leucine (Leu-CUN or L) 12,266–12,336 H
MT-TK transfer RNA tRNA-Lysine (Lys or K) 08,295–08,364 H
MT-TM transfer RNA tRNA-Methionine (Met or M) 04,402–04,469 H
MT-TF transfer RNA tRNA-Phenylalanine (Phe or F) 00,577–00,647 H
MT-TP transfer RNA tRNA-Proline (Pro or P) 15,956–16,023 L
MT-TS1 transfer RNA tRNA-Serine (Ser-UCN or S) 07,446–07,514 L
MT-TS2 transfer RNA tRNA-Serine (Ser-AGY or S) 12,207–12,265 H
MT-TT transfer RNA tRNA-Threonine (Thr or T) 15,888–15,953 H
MT-TW transfer RNA tRNA-Tryptophan (Trp or W) 05,512–05,579 H
MT-TY transfer RNA tRNA-Tyrosine (Tyr or Y) 05,826–05,891 L
MT-TV transfer RNA tRNA-Valine (Val or V) 01,602–01,670 H
MT-RNR1 ribosomal RNA Small subunit : SSU (12S) 00,648–01,601 H
MT-RNR2 ribosomal RNA Large subunit : LSU (16S) 01,671–03,229 H

Between most (but not all) protein-coding regions, tRNAs are present (see the human mitochondrial genome map). During transcription, the tRNAs acquire their characteristic L-shape that gets recognized and cleaved by specific enzymes. With the mitochondrial RNA processing, individual mRNA, rRNA, and tRNA sequences are released from the primary transcript.[39] Folded tRNAs therefore act as secondary structure punctuations.[40]

Regulation of transcription

The promoters for the initiation of the transcription of the heavy and light strands are located in the main non-coding region of the mtDNA called the displacement loop, the D-loop.[36] There is evidence that the transcription of the mitochondrial rRNAs is regulated by the heavy-strand promoter 1 (HSP1), and the transcription of the polycistronic transcripts coding for the protein subunits are regulated by HSP2.[36]

Measurement of the levels of the mtDNA-encoded RNAs in bovine tissues has shown that there are major differences in the expression of the mitochondrial RNAs relative to total tissue RNA.[41] Among the 12 tissues examined the highest level of expression was observed in heart, followed by brain and steroidogenic tissue samples.[41]

As demonstrated by the effect of the trophic hormone ACTH on adrenal cortex cells, the expression of the mitochondrial genes may be strongly regulated by external factors, apparently to enhance the synthesis of mitochondrial proteins necessary for energy production.[41] Interestingly, while the expression of protein-encoding genes was stimulated by ACTH, the levels of the mitochondrial 16S rRNA showed no significant change.[41]

Mitochondrial inheritance

In most multicellular organisms, mtDNA is inherited from the mother (maternally inherited). Mechanisms for this include simple dilution (an egg contains on average 200,000 mtDNA molecules, whereas a healthy human sperm has been reported to contain on average 5 molecules),[42][43] degradation of sperm mtDNA in the male genital tract and in the fertilized egg; and, at least in a few organisms, failure of sperm mtDNA to enter the egg. Whatever the mechanism, this single parent (uniparental inheritance) pattern of mtDNA inheritance is found in most animals, most plants and also in fungi.[44]

In a study published in 2018, human babies were reported to inherit mtDNA from both their fathers and their mothers resulting in mtDNA heteroplasmy,[45] a finding that has been rejected by other scientists.[46][47][48]

Female inheritance

In sexual reproduction, mitochondria are normally inherited exclusively from the mother; the mitochondria in mammalian sperm are usually destroyed by the egg cell after fertilization. Also, mitochondria are only in the sperm tail, which is used for propelling the sperm cells and sometimes the tail is lost during fertilization. In 1999 it was reported that paternal sperm mitochondria (containing mtDNA) are marked with ubiquitin to select them for later destruction inside the embryo.[49] Some in vitro fertilization techniques, particularly injecting a sperm into an oocyte, may interfere with this.

The fact that mitochondrial DNA is mostly maternally inherited enables genealogical researchers to trace maternal lineage far back in time. (Y-chromosomal DNA, paternally inherited, is used in an analogous way to determine the patrilineal history.) This is usually accomplished on human mitochondrial DNA by sequencing the hypervariable control regions (HVR1 or HVR2), and sometimes the complete molecule of the mitochondrial DNA, as a genealogical DNA test.[50] HVR1, for example, consists of about 440 base pairs. These 440 base pairs are compared to the same regions of other individuals (either specific people or subjects in a database) to determine maternal lineage. Most often, the comparison is made with the revised Cambridge Reference Sequence. Vilà et al. have published studies tracing the matrilineal descent of domestic dogs from wolves.[51] The concept of the Mitochondrial Eve is based on the same type of analysis, attempting to discover the origin of humanity by tracking the lineage back in time.

The mitochondrial bottleneck

Entities subject to uniparental inheritance and with little to no recombination may be expected to be subject to Muller's ratchet, the accumulation of deleterious mutations until functionality is lost. Animal populations of mitochondria avoid this through a developmental process known as the mtDNA bottleneck. The bottleneck exploits random processes in the cell to increase the cell-to-cell variability in mutant load as an organism develops: a single egg cell with some proportion of mutant mtDNA thus produces an embryo in which different cells have different mutant loads. Cell-level selection may then act to remove those cells with more mutant mtDNA, leading to a stabilisation or reduction in mutant load between generations. The mechanism underlying the bottleneck is debated,[52][53][54][55] with a recent mathematical and experimental metastudy providing evidence for a combination of the random partitioning of mtDNAs at cell divisions and the random turnover of mtDNA molecules within the cell.[33]

Male inheritance

Main page: Biology:Paternal mtDNA transmission

Male mitochondrial DNA inheritance has been discovered in Plymouth Rock chickens.[56] Evidence supports rare instances of male mitochondrial inheritance in some mammals as well. Specifically, documented occurrences exist for mice,[57][58] where the male-inherited mitochondria were subsequently rejected. It has also been found in sheep,[59] and in cloned cattle.[60] Rare cases of male mitochondrial inheritance have been documented in humans.[61][62][63][45] Although many of these cases involve cloned embryos or subsequent rejection of the paternal mitochondria, others document in vivo inheritance and persistence under lab conditions.

Doubly uniparental inheritance of mtDNA is observed in bivalve mollusks. In those species, females have only one type of mtDNA (F), whereas males have F type mtDNA in their somatic cells, but M type of mtDNA (which can be as much as 30% divergent) in germline cells.[64] Paternally inherited mitochondria have additionally been reported in some insects such as fruit flies,[65][66] honeybees,[67] and periodical cicadas.[68]

Mitochondrial donation

An IVF technique known as mitochondrial donation or mitochondrial replacement therapy (MRT) results in offspring containing mtDNA from a donor female, and nuclear DNA from the mother and father. In the spindle transfer procedure, the nucleus of an egg is inserted into the cytoplasm of an egg from a donor female which has had its nucleus removed, but still contains the donor female's mtDNA. The composite egg is then fertilized with the male's sperm. The procedure is used when a woman with genetically defective mitochondria wishes to procreate and produce offspring with healthy mitochondria.[69] The first known child to be born as a result of mitochondrial donation was a boy born to a Jordanian couple in Mexico on 6 April 2016.[70]

Mutations and disease

Human mitochondrial DNA with groups of protein-, rRNA- and tRNA-encoding genes
The involvement of mitochondrial DNA in several human diseases

Susceptibility

The concept that mtDNA is particularly susceptible to reactive oxygen species generated by the respiratory chain due to its proximity remains controversial.[71] mtDNA does not accumulate any more oxidative base damage than nuclear DNA.[72] It has been reported that at least some types of oxidative DNA damage are repaired more efficiently in mitochondria than they are in the nucleus.[73] mtDNA is packaged with proteins which appear to be as protective as proteins of the nuclear chromatin.[74] Moreover, mitochondria evolved a unique mechanism which maintains mtDNA integrity through degradation of excessively damaged genomes followed by replication of intact/repaired mtDNA. This mechanism is not present in the nucleus and is enabled by multiple copies of mtDNA present in mitochondria.[75] The outcome of mutation in mtDNA may be an alteration in the coding instructions for some proteins,[76] which may have an effect on organism metabolism and/or fitness.

Genetic illness

Further information: Medicine:Mitochondrial disease

Mutations of mitochondrial DNA can lead to a number of illnesses including exercise intolerance and Kearns–Sayre syndrome (KSS), which causes a person to lose full function of heart, eye, and muscle movements. Some evidence suggests that they might be major contributors to the aging process and age-associated pathologies.[77] Particularly in the context of disease, the proportion of mutant mtDNA molecules in a cell is termed heteroplasmy. The within-cell and between-cell distributions of heteroplasmy dictate the onset and severity of disease[78] and are influenced by complicated stochastic processes within the cell and during development.[33][79]

Mutations in mitochondrial tRNAs can be responsible for severe diseases like the MELAS and MERRF syndromes.[80]

Mutations in nuclear genes that encode proteins that mitochondria use can also contribute to mitochondrial diseases. These diseases do not follow mitochondrial inheritance patterns, but instead follow Mendelian inheritance patterns.[81]

Use in disease diagnosis

Recently a mutation in mtDNA has been used to help diagnose prostate cancer in patients with negative prostate biopsy.[82][83] mtDNA alterations can be detected in the bio-fluids of patients with cancer.[84] mtDNA is characterized by the high rate of polymorphisms and mutations. Some of which are increasingly recognized as an important cause of human pathology such as oxidative phosphorylation (OXPHOS) disorders, maternally inherited diabetes and deafness (MIDD), Type 2 diabetes mellitus, Neurodegenerative disease, heart failure and cancer.

Relationship with ageing

Though the idea is controversial, some evidence suggests a link between aging and mitochondrial genome dysfunction.[85] In essence, mutations in mtDNA upset a careful balance of reactive oxygen species (ROS) production and enzymatic ROS scavenging (by enzymes like superoxide dismutase, catalase, glutathione peroxidase and others). However, some mutations that increase ROS production (e.g., by reducing antioxidant defenses) in worms increase, rather than decrease, their longevity.[71] Also, naked mole rats, rodents about the size of mice, live about eight times longer than mice despite having reduced, compared to mice, antioxidant defenses and increased oxidative damage to biomolecules.[86] Once, there was thought to be a positive feedback loop at work (a 'Vicious Cycle'); as mitochondrial DNA accumulates genetic damage caused by free radicals, the mitochondria lose function and leak free radicals into the cytosol. A decrease in mitochondrial function reduces overall metabolic efficiency.[87] However, this concept was conclusively disproved when it was demonstrated that mice, which were genetically altered to accumulate mtDNA mutations at accelerated rate do age prematurely, but their tissues do not produce more ROS as predicted by the 'Vicious Cycle' hypothesis.[88] Supporting a link between longevity and mitochondrial DNA, some studies have found correlations between biochemical properties of the mitochondrial DNA and the longevity of species.[89] The application of a mitochondrial-specific ROS scavenger, which lead to a significant longevity of the mice studied,[90] suggests that mitochondria may still be well-implicated in ageing. Extensive research is being conducted to further investigate this link and methods to combat ageing. Presently, gene therapy and nutraceutical supplementation are popular areas of ongoing research.[91][92] Bjelakovic et al. analyzed the results of 78 studies between 1977 and 2012, involving a total of 296,707 participants, and concluded that antioxidant supplements do not reduce all-cause mortality nor extend lifespan, while some of them, such as beta carotene, vitamin E, and higher doses of vitamin A, may actually increase mortality.[93] In a recent study, it was showed that dietary restriction can reverse ageing alterations by affecting the accumulation of mtDNA damage in several organs of rats. For example, dietary restriction prevented age-related accumulation of mtDNA damage in the cortex and decreased it in the lung and testis.[94]

Neurodegenerative diseases

Increased mtDNA damage is a feature of several neurodegenerative diseases.

The brains of individuals with Alzheimer’s disease have elevated levels of oxidative DNA damage in both nuclear DNA and mtDNA, but the mtDNA has approximately 10-fold higher levels than nuclear DNA.[95] It has been proposed that aged mitochondria is the critical factor in the origin of neurodegeneration in Alzheimer’s disease.[96] Analysis of the brains of AD patients suggested an impaired function of the DNA repair pathway, which would cause reduce the overall quality of mtDNA.[97]

In Huntington’s disease, mutant huntingtin protein causes mitochondrial dysfunction involving inhibition of mitochondrial electron transport, higher levels of reactive oxygen species and increased oxidative stress.[98] Mutant huntingtin protein promotes oxidative damage to mtDNA, as well as nuclear DNA, that may contribute to Huntington’s disease pathology.[99]

The DNA oxidation product 8-oxoguanine (8-oxoG) is a well-established marker of oxidative DNA damage. In persons with amyotrophic lateral sclerosis (ALS), the enzymes that normally repair 8-oxoG DNA damages in the mtDNA of spinal motor neurons are impaired.[100] Thus oxidative damage to mtDNA of motor neurons may be a significant factor in the etiology of ALS.

Correlation of the mtDNA base composition with animal life spans

Animal species mtDNA base composition was retrieved from the MitoAge database and compared to their maximum life span from AnAge database.

Over the past decade, an Israeli research group led by Professor Vadim Fraifeld has shown that strong and significant correlations exist between the mtDNA base composition and animal species-specific maximum life spans.[101][102][103] As demonstrated in their work, higher mtDNA guanine + cytosine content (GC%) strongly associates with longer maximum life spans across animal species. An additional observation is that the mtDNA GC% correlation with the maximum life spans is independent of the well-known correlation between animal species metabolic rate and maximum life spans. The mtDNA GC% and resting metabolic rate explain the differences in animal species maximum life spans in a multiplicative manner (i.e., species maximum life span = their mtDNA GC% * metabolic rate).[102] To support the scientific community in carrying out comparative analyses between mtDNA features and longevity across animals, a dedicated database was built named MitoAge.[104]

mtDNA mutational spectrum is sensitive to species-specific life-history traits

De novo mutations arise either due to mistakes during DNA replication or due to unrepaired damage caused in turn by endogenous and exogenous mutagens. It has been long believed that mtDNA can be particularly sensitive to damage caused by reactive oxygen species (ROS), however G>T substitutions, the hallmark of the oxidative damage in the nuclear genome, are very rare in mtDNA and do not increase with age. Comparing the mtDNA mutational spectra of hundreds of mammalian species, it has been recently demonstrated that species with extended lifespans have an increased rate of A>G substitutions on single-stranded heavy chain.[105] This discovery led to the hypothesis that A>G is a mitochondria-specific marker of age-associated oxidative damage. This finding provides a mutational (contrary to the selective one) explanation for the observation that long-lived species have GC-rich mtDNA: long-lived species become GC-rich simply because of their biased process of mutagenesis. An association between mtDNA mutational spectrum and species-specific life-history traits in mammals opens a possibility to link these factors together discovering new life-history-specific mutagens in different groups of organisms.

Relationship with non-B (non-canonical) DNA structures

Deletion breakpoints frequently occur within or near regions showing non-canonical (non-B) conformations, namely hairpins, cruciforms and cloverleaf-like elements.[106] Moreover, there is data supporting the involvement of helix-distorting intrinsically curved regions and long G-tetrads in eliciting instability events. In addition, higher breakpoint densities were consistently observed within GC-skewed regions and in the close vicinity of the degenerate sequence motif YMMYMNNMMHM.[107]

Use in forensics

Unlike nuclear DNA, which is inherited from both parents and in which genes are rearranged in the process of recombination, there is usually no change in mtDNA from parent to offspring. Although mtDNA also recombines, it does so with copies of itself within the same mitochondrion. Because of this and because the mutation rate of animal mtDNA is higher than that of nuclear DNA,[108] mtDNA is a powerful tool for tracking ancestry through females (matrilineage) and has been used in this role to track the ancestry of many species back hundreds of generations.

mtDNA testing can be used by forensic scientists in cases where nuclear DNA is severely degraded. Autosomal cells only have two copies of nuclear DNA, but can have hundreds of copies of mtDNA due to the multiple mitochondria present in each cell. This means highly degraded evidence that would not be beneficial for STR analysis could be used in mtDNA analysis. mtDNA may be present in bones, teeth, or hair, which could be the only remains left in the case of severe degradation. In contrast to STR analysis, mtDNA sequencing uses Sanger sequencing. The known sequence and questioned sequence are both compared to the Revised Cambridge Reference Sequence to generate their respective haplotypes. If the known sample sequence and questioned sequence originated from the same matriline, one would expect to see identical sequences and identical differences from the rCRS.[109] Cases arise where there are no known samples to collect and the unknown sequence can be searched in a database such as EMPOP. The Scientific Working Group on DNA Analysis Methods recommends three conclusions for describing the differences between a known mtDNA sequence and a questioned mtDNA sequence: exclusion for two or more differences between the sequences, inconclusive if there is one nucleotide difference, or cannot exclude if there are no nucleotide differences between the two sequences.[110]

The rapid mutation rate (in animals) makes mtDNA useful for assessing genetic relationships of individuals or groups within a species and also for identifying and quantifying the phylogeny (evolutionary relationships; see phylogenetics) among different species. To do this, biologists determine and then compare the mtDNA sequences from different individuals or species. Data from the comparisons is used to construct a network of relationships among the sequences, which provides an estimate of the relationships among the individuals or species from which the mtDNAs were taken. mtDNA can be used to estimate the relationship between both closely related and distantly related species. Due to the high mutation rate of mtDNA in animals, the 3rd positions of the codons change relatively rapidly, and thus provide information about the genetic distances among closely related individuals or species. On the other hand, the substitution rate of mt-proteins is very low, thus amino acid changes accumulate slowly (with corresponding slow changes at 1st and 2nd codon positions) and thus they provide information about the genetic distances of distantly related species. Statistical models that treat substitution rates among codon positions separately, can thus be used to simultaneously estimate phylogenies that contain both closely and distantly related species[80]

Mitochondrial DNA was admitted into evidence for the first time ever in a United States courtroom in 1996 during State of Tennessee v. Paul Ware.[111]

In the 1998 United States court case of Commonwealth of Pennsylvania v. Patricia Lynne Rorrer,[112] mitochondrial DNA was admitted into evidence in the State of Pennsylvania for the first time.[113][114] The case was featured in episode 55 of season 5 of the true crime drama series Forensic Files (season 5).[115]

Mitochondrial DNA was first admitted into evidence in California , United States, in the successful prosecution of David Westerfield for the 2002 kidnapping and murder of 7-year-old Danielle van Dam in San Diego: it was used for both human and dog identification.[116] This was the first trial in the U.S. to admit canine DNA.[117]

The remains of King Richard III, who died in 1485, were identified by comparing his mtDNA with that of two matrilineal descendants of his sister who were alive in 2013, 527 years after he died.[118]

Use in evolutionary biology and systematic biology

mtDNA is conserved across eukaryotic organism given the critical role of mitochondria in cellular respiration. However, due to less efficient DNA repair (compared to nuclear DNA) it has a relatively high mutation rate (but slow compared to other DNA regions such as microsatellites) which makes it useful for studying the evolutionary relationships—phylogeny—of organisms. Biologists can determine and then compare mtDNA sequences among different species and use the comparisons to build an evolutionary tree for the species examined.

For instance, while most nuclear genes are nearly identical between humans and chimpanzees, their mitochondrial genomes are 9.8% different. Human and gorilla mitochondrial genomes are 11.8% different, suggesting that humans may be more closely related to chimpanzees than gorillas.[119]

mtDNA in nuclear DNA

Whole genome sequences of more than 66,000 people revealed that most of them had some mitochondrial DNA inserted into their nuclear genomes. More than 90% of these nuclear-mitochondrial segments (NUMTs) were inserted after humans diverged from apes. Results indicate such transfers currently occur as frequent as once in every ~4,000 human births.[120]

It appears that organellar DNA is much more often transferred to nuclear DNA than previously thought. This observation also supports the idea of the endosymbiont theory that eukaryotes have evolved from endosymbionts which turned into organelles while transferring most of their DNA to the nucleus so that the organellar genome shrunk in the process.[121]

History

Mitochondrial DNA was discovered in the 1960s by Margit M. K. Nass and Sylvan Nass by electron microscopy as DNase-sensitive threads inside mitochondria,[122] and by Ellen Haslbrunner, Hans Tuppy and Gottfried Schatz by biochemical assays on highly purified mitochondrial fractions.[123]

Mitochondrial sequence databases

Several specialized databases have been founded to collect mitochondrial genome sequences and other information. Although most of them focus on sequence data, some of them include phylogenetic or functional information.

  • AmtDB: a database of ancient human mitochondrial genomes.[124]
  • InterMitoBase: an annotated database and analysis platform of protein-protein interactions for human mitochondria.[125] (apparently last updated in 2010, but still available)
  • MitoBreak: the mitochondrial DNA breakpoints database.[126]
  • MitoFish and MitoAnnotator: a mitochondrial genome database of fish.[127] See also Cawthorn et al.[128]
  • Mitome: a database for comparative mitochondrial genomics in metazoan animals[129] (no longer available)
  • MitoRes: a resource of nuclear-encoded mitochondrial genes and their products in metazoa[130] (apparently no longer being updated)
  • MitoSatPlant: Mitochondrial microsatellites database of viridiplantae.[131]
  • MitoZoa 2.0: a database for comparative and evolutionary analyses of mitochondrial genomes in Metazoa.[132] (no longer available)

MtDNA-phenotype association databases

Genome-wide association studies can reveal associations of mtDNA genes and their mutations with phenotypes including lifespan and disease risks. In 2021, the largest, UK Biobank-based, genome-wide association study of mitochondrial DNA unveiled 260 new associations with phenotypes including lifespan and disease risks for e.g. type 2 diabetes.[133][134]

Mitochondrial mutation databases

Several specialized databases exist that report polymorphisms and mutations in the human mitochondrial DNA, together with the assessment of their pathogenicity.

See also

References

  1. ↑ "Powerhouse of the cell". Scientific American 197 (1): 131–40. 1957. doi:10.1038/scientificamerican0757-131. Bibcode: 1957SciAm.197a.131S. 
  2. ↑ "The functional organization of mitochondrial genomes in human cells". BMC Biology 2: 9. May 2004. doi:10.1186/1741-7007-2-9. PMID 15157274. 
  3. ↑ "Mitochondrial DNA and human history". The Human Genome. Wellcome Trust. 10 September 2003. http://genome.wellcome.ac.uk/doc_WTD020876.html. 
  4. ↑ "Sequence and organization of the human mitochondrial genome". Nature 290 (5806): 457–465. April 1981. doi:10.1038/290457a0. PMID 7219534. Bibcode: 1981Natur.290..457A. 
  5. ↑ "[Not Available"]. Génétique, Sélection, Évolution 18 (1): 73–98. 1986-01-01. doi:10.1186/1297-9686-18-1-73. PMID 22879234. 
  6. ↑ "Molecular systematics of armadillos (Xenarthra, Dasypodidae): contribution of maximum likelihood and Bayesian analyses of mitochondrial and nuclear genes". Molecular Phylogenetics and Evolution 28 (2): 261–275. August 2003. doi:10.1016/s1055-7903(03)00111-8. PMID 12878463. https://hal.archives-ouvertes.fr/halsde-00192983. Retrieved 4 November 2018. 
  7. ↑ "Combining multiple autosomal introns for studying shallow phylogeny and taxonomy of Laurasiatherian mammals: Application to the tribe Bovini (Cetartiodactyla, Bovidae)". Molecular Phylogenetics and Evolution 66 (3): 766–775. March 2013. doi:10.1016/j.ympev.2012.11.003. PMID 23159894. 
  8. ↑ 8.0 8.1 8.2 "Evolutionary Inference across Eukaryotes Identifies Specific Pressures Favoring Mitochondrial Gene Retention". Cell Systems 2 (2): 101–111. February 2016. doi:10.1016/j.cels.2016.01.013. PMID 27135164. 
  9. ↑ "Mitochondrion‐Derived Organelles in Protists and Fungi". A Survey of Cell Biology. International Review of Cytology. 244. 2005. pp. 175–225. doi:10.1016/S0074-7696(05)44005-X. ISBN 978-0-12-364648-4. 
  10. ↑ "Evolution of mitochondrial gene content: gene loss and transfer to the nucleus". Molecular Phylogenetics and Evolution 29 (3): 380–395. December 2003. doi:10.1016/S1055-7903(03)00194-5. PMID 14615181. 
  11. ↑ "Mitochondrial genomes are retained by selective constraints on protein targeting". Proceedings of the National Academy of Sciences of the United States of America 112 (33): 10154–10161. August 2015. doi:10.1073/pnas.1421372112. PMID 26195779. Bibcode: 2015PNAS..11210154B. 
  12. ↑ "Why chloroplasts and mitochondria retain their own genomes and genetic systems: Colocation for redox regulation of gene expression". Proceedings of the National Academy of Sciences of the United States of America 112 (33): 10231–10238. August 2015. doi:10.1073/pnas.1500012112. PMID 26286985. Bibcode: 2015PNAS..11210231A. 
  13. ↑ 13.0 13.1 "Diversity of mitochondrial genome organization". Biochemistry. Biokhimiia 77 (13): 1424–1435. December 2012. doi:10.1134/S0006297912130020. PMID 23379519. 
  14. ↑ "Linear mitochondrial genomes: 30 years down the line". Trends in Genetics 14 (5): 184–188. May 1998. doi:10.1016/S0168-9525(98)01443-7. PMID 9613202. 
  15. ↑ "Animal Mitochondrial DNA as We Do Not Know It: mt-Genome Organization and Evolution in Nonbilaterian Lineages". Genome Biology and Evolution 8 (9): 2896–2913. September 2016. doi:10.1093/gbe/evw195. PMID 27557826. 
  16. ↑ 16.0 16.1 Boore, J. L. (1 April 1999). "Animal mitochondrial genomes". Nucleic Acids Research 27 (8): 1767–1780. doi:10.1093/nar/27.8.1767. PMID 10101183. 
  17. ↑ "Linear Mitochondrial Genome in Anthozoa (Cnidaria): A Case Study in Ceriantharia". Scientific Reports 9 (1): 6094. April 2019. doi:10.1038/s41598-019-42621-z. PMID 30988357. Bibcode: 2019NatSR...9.6094S. 
  18. ↑ Polymorphism within the mitochondrial genome of the ctenophore, Pleurobrachia bachei and its ongoing rapid evolution - bioRxiv
  19. ↑ "A cnidarian parasite of salmon (Myxozoa: Henneguya) lacks a mitochondrial genome". Proceedings of the National Academy of Sciences of the United States of America 117 (10): 5358–5363. March 2020. doi:10.1073/pnas.1909907117. PMID 32094163. Bibcode: 2020PNAS..117.5358Y. 
  20. ↑ "Scientists Find The First-Ever Animal That Doesn't Need Oxygen to Survive" (in en-gb). 25 February 2020. https://www.sciencealert.com/this-is-the-first-known-animal-that-doesn-t-need-oxygen-to-survive. 
  21. ↑ de Queiroz, Casley Borges; Santana, Mateus Ferreira; Pereira Vidigal, Pedro M.; de Queiroz, Marisa Vieira (2018-03-15). "Comparative analysis of the mitochondrial genome of the fungus Colletotrichum lindemuthianum, the causal agent of anthracnose in common beans". Applied Microbiology & Biotechnology 102 (6): 2763–2778. doi:10.1007/s00253-018-8812-0. PMID 29453633. https://dx.doi.org/10.1007/s00253-018-8812-0. 
  22. ↑ Masutani, Bansho; Arimura, Shin-ichi; Morishita, Shinichi (2021-01-12). "Investigating the mitochondrial genomic landscape of Arabidopsis thaliana by long-read sequencing". PLOS Computational Biology 17 (1): e1008597. doi:10.1371/journal.pcbi.1008597. PMID 33434206. Bibcode: 2021PLSCB..17E8597M. 
  23. ↑ Kozik, Alexander; Rowan, Beth A.; Lavelle, Dean; Berke, Lidija; Schranz, M. Eric; Michelmore, Richard W.; Christensen, Alan C. (2019-08-30). "The alternative reality of plant mitochondrial DNA: One ring does not rule them all". PLOS Genetics 15 (8): e1008373. doi:10.1371/journal.pgen.1008373. PMID 31469821. 
  24. ↑ "Global Characterization of Fungal Mitogenomes: New Insights on Genomic Diversity and Dynamism of Coding Genes and Accessory Elements". Frontiers in Microbiology 12: 787283. 2021. doi:10.3389/fmicb.2021.787283. PMID 34925295. 
  25. ↑ "Rapid evolution of enormous, multichromosomal genomes in flowering plant mitochondria with exceptionally high mutation rates". PLOS Biology 10 (1): e1001241. January 2012. doi:10.1371/journal.pbio.1001241. PMID 22272183. 
  26. ↑ "The mitochondrial genome is large and variable in a family of plants (cucurbitaceae)". Cell 25 (3): 793–803. September 1981. doi:10.1016/0092-8674(81)90187-2. PMID 6269758. 
  27. ↑ "Origins and recombination of the bacterial-sized multichromosomal mitochondrial genome of cucumber". The Plant Cell 23 (7): 2499–2513. July 2011. doi:10.1105/tpc.111.087189. PMID 21742987. 
  28. ↑ "Mitochondrial DNA (mtDNA)". Integrated DNA Technologies. https://www.idtdna.com/pages/docs/educational-resources/mitochondrial-dna.pdf?sfvrsn=4. 
  29. ↑ "Whole mitochondrial genome sequence of an Indian Plasmodium falciparum field isolate". The Korean Journal of Parasitology 52 (1): 99–103. February 2014. doi:10.3347/kjp.2014.52.1.99. PMID 24623891. 
  30. ↑ "Functional human mitochondrial DNA polymerase gamma forms a heterotrimer". The Journal of Biological Chemistry 281 (1): 374–382. January 2006. doi:10.1074/jbc.M509730200. PMID 16263719. 
  31. ↑ "The mitochondrial DNA helicase TWINKLE can assemble on a closed circular template and support initiation of DNA synthesis". Nucleic Acids Research 39 (21): 9238–9249. November 2011. doi:10.1093/nar/gkr653. PMID 21840902. 
  32. ↑ 32.0 32.1 32.2 "Mitochondrial DNA transmission, replication and inheritance: a journey from the gamete through the embryo and into offspring and embryonic stem cells". Human Reproduction Update 16 (5): 488–509. 2010. doi:10.1093/humupd/dmq002. PMID 20231166. 
  33. ↑ 33.0 33.1 33.2 "Stochastic modelling, Bayesian inference, and new in vivo measurements elucidate the debated mtDNA bottleneck mechanism". eLife 4: e07464. June 2015. doi:10.7554/eLife.07464. PMID 26035426. 
  34. ↑ "Mitochondrial DNA in anucleate human blood cells". Biochemical and Biophysical Research Communications 155 (3): 1360–1365. September 1988. doi:10.1016/s0006-291x(88)81291-9. PMID 3178814. 
  35. ↑ "Mitochondria in oocyte aging: current understanding". Facts, Views & Vision in ObGyn 9 (1): 29–38. March 2017. PMID 28721182. 
  36. ↑ 36.0 36.1 36.2 "Mitochondrial DNA Transcription and Its Regulation: An Evolutionary Perspective". Trends in Genetics 34 (9): 682–692. September 2018. doi:10.1016/j.tig.2018.05.009. PMID 29945721. 
  37. ↑ "Transcription, Processing, and Decay of Mitochondrial RNA in Health and Disease". International Journal of Molecular Sciences 20 (9): 2221. May 2019. doi:10.3390/ijms20092221. PMID 31064115. 
  38. ↑ Homo sapiens mitochondrion, complete genome. "Revised Cambridge Reference Sequence (rCRS): accession NC_012920" , National Center for Biotechnology Information. Retrieved on 20 February 2017.
  39. ↑ "DNA replication and transcription in mammalian mitochondria". Annual Review of Biochemistry 76 (1): 679–699. 2007-06-19. doi:10.1146/annurev.biochem.76.060305.152028. PMID 17408359. 
  40. ↑ "tRNA punctuation model of RNA processing in human mitochondria". Nature 290 (5806): 470–474. April 1981. doi:10.1038/290470a0. PMID 7219536. Bibcode: 1981Natur.290..470O. 
  41. ↑ 41.0 41.1 41.2 41.3 "Mitochondrial-genome-encoded RNAs: differential regulation by corticotropin in bovine adrenocortical cells". Proceedings of the National Academy of Sciences of the United States of America 90 (22): 10509–10513. November 1993. doi:10.1073/pnas.90.22.10509. PMID 7504267. Bibcode: 1993PNAS...9010509R. 
  42. ↑ "Lost in the zygote: the dilution of paternal mtDNA upon fertilization". Heredity 101 (5): 429–434. November 2008. doi:10.1038/hdy.2008.74. PMID 18685570. 
  43. ↑ "Influence of microsurgical varicocelectomy on human sperm mitochondrial DNA copy number: a pilot study". Journal of Assisted Reproduction and Genetics 29 (8): 759–764. August 2012. doi:10.1007/s10815-012-9785-z. PMID 22562241. 
  44. ↑ "Mitochondrial Inheritance in Phytopathogenic Fungi-Everything Is Known, or Is It?". Int J Mol Sci 21 (11): 3883. May 2020. doi:10.3390/ijms21113883. PMID 32485941. 
  45. ↑ 45.0 45.1 "Biparental Inheritance of Mitochondrial DNA in Humans". Proceedings of the National Academy of Sciences of the United States of America 115 (51): 13039–13044. December 2018. doi:10.1073/pnas.1810946115. PMID 30478036. Bibcode: 2018PNAS..11513039L. 
  46. ↑ "Biparental inheritance of mitochondrial DNA revisited". Nature Reviews. Genetics 22 (8): 477–478. August 2021. doi:10.1038/s41576-021-00380-6. PMID 34031572. https://discovery.ucl.ac.uk/id/eprint/10128999/. 
  47. ↑ "Extraordinary claims require extraordinary evidence in asserted mtDNA biparental inheritance". Forensic Science International. Genetics 47: 102274. July 2020. doi:10.1016/j.fsigen.2020.102274. PMID 32330850. 
  48. ↑ "Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans". Nature Communications 11 (1): 1740. April 2020. doi:10.1038/s41467-020-15336-3. PMID 32269217. Bibcode: 2020NatCo..11.1740W. 
  49. ↑ "Ubiquitin tag for sperm mitochondria". Nature 402 (6760): 371–372. November 1999. doi:10.1038/46466. PMID 10586873. Bibcode: 1999Natur.402..371S.  Discussed in: "Mom's Eggs Execute Dad's Mitochondria". Science News 157 (1): 5. 2000. doi:10.2307/4012086. https://www.sciencenews.org/article/moms-eggs-execute-dads-mitochondria. 
  50. ↑ "Hiring a DNA Testing Company Genealogy". The Church of Jesus Christ of Latter-day Saints. 2016. https://familysearch.org/wiki/en/Hiring_a_DNA_Testing_Company. 
  51. ↑ "Multiple and ancient origins of the domestic dog". Science 276 (5319): 1687–1689. June 1997. doi:10.1126/science.276.5319.1687. PMID 9180076. https://www.consevol.org/pdf/Vila_1997_Science_1.pdf. 
  52. ↑ "The strength and timing of the mitochondrial bottleneck in salmon suggests a conserved mechanism in vertebrates". PLOS ONE 6 (5): e20522. 2011. doi:10.1371/journal.pone.0020522. PMID 21655224. Bibcode: 2011PLoSO...620522W. 
  53. ↑ "A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes". Nature Genetics 40 (2): 249–254. February 2008. doi:10.1038/ng.2007.63. PMID 18223651. 
  54. ↑ "The mitochondrial bottleneck occurs without reduction of mtDNA content in female mouse germ cells". Nature Genetics 39 (3): 386–390. March 2007. doi:10.1038/ng1970. PMID 17293866. 
  55. ↑ "The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes". Nature Genetics 40 (12): 1484–1488. December 2008. doi:10.1038/ng.258. PMID 19029901. 
  56. ↑ "Mitogenomic analysis of a 50-generation chicken pedigree reveals a rapid rate of mitochondrial evolution and evidence for paternal mtDNA inheritance". Biology Letters 11 (10): 20150561. October 2015. doi:10.1098/rsbl.2015.0561. PMID 26510672. 
  57. ↑ "Paternal inheritance of mitochondrial DNA in mice". Nature 352 (6332): 255–257. July 1991. doi:10.1038/352255a0. PMID 1857422. Bibcode: 1991Natur.352..255G. 
  58. ↑ "Maternal inheritance of mouse mtDNA in interspecific hybrids: segregation of the leaked paternal mtDNA followed by the prevention of subsequent paternal leakage". Genetics 148 (2): 851–857. February 1998. doi:10.1093/genetics/148.2.851. PMID 9504930. 
  59. ↑ "Further evidence for paternal inheritance of mitochondrial DNA in the sheep (Ovis aries)". Heredity 93 (4): 399–403. October 2004. doi:10.1038/sj.hdy.6800516. PMID 15266295. 
  60. ↑ "Composition of parental mitochondrial DNA in cloned bovine embryos". FEBS Letters 426 (3): 352–356. April 1998. doi:10.1016/S0014-5793(98)00350-0. PMID 9600265. 
  61. ↑ "A105 Family Decoded: Discovery of Genome-Wide Fingerprints for Personalized Genomic Medicine". ScienceMED 3 (2): 115–126. April 2012. 
  62. ↑ "Customized Biomedical Informatics". BMC Big Data Analytics 3. May 2018. doi:10.1186/s41044-018-0030-3. 
  63. ↑ "Paternal inheritance of mitochondrial DNA". The New England Journal of Medicine 347 (8): 576–580. August 2002. doi:10.1056/NEJMoa020350. PMID 12192017. 
  64. ↑ "Doubly uniparental inheritance: two mitochondrial genomes, one precious model for organelle DNA inheritance and evolution". DNA and Cell Biology 28 (2): 79–89. February 2009. doi:10.1089/dna.2008.0807. PMID 19196051. 
  65. ↑ "Further observation of paternal transmission of Drosophila mitochondrial DNA by PCR selective amplification method". Genetical Research 59 (2): 81–84. April 1992. doi:10.1017/S0016672300030287. PMID 1628820. 
  66. ↑ "Paternal transmission of mitochondrial DNA as an integral part of mitochondrial inheritance in metapopulations of Drosophila simulans". Heredity 110 (1): 57–62. January 2013. doi:10.1038/hdy.2012.60. PMID 23010820. 
  67. ↑ "Transfer of paternal mitochondrial DNA during fertilization of honeybee (Apis mellifera L.) eggs". Current Genetics 24 (6): 539–543. December 1993. doi:10.1007/BF00351719. PMID 8299176. 
  68. ↑ "Evidence for paternal leakage in hybrid periodical cicadas (Hemiptera: Magicicada spp.)". PLOS ONE 2 (9): e892. September 2007. doi:10.1371/journal.pone.0000892. PMID 17849021. Bibcode: 2007PLoSO...2..892F. 
  69. ↑ "Ban on scientists trying to create three-parent baby". The Independent. 14 October 2003. https://www.independent.co.uk/news/science/ban-on-scientists-trying-to-create-threeparent-baby-583284.html. [yes|permanent dead link|dead link}}]
  70. ↑ "First 'three person baby' born using new method" (in en-GB). BBC News. 2016-09-27. https://www.bbc.co.uk/news/health-37485263. 
  71. ↑ 71.0 71.1 "Is there more to aging than mitochondrial DNA and reactive oxygen species?". The FEBS Journal 276 (20): 5768–5787. October 2009. doi:10.1111/j.1742-4658.2009.07269.x. PMID 19796285. 
  72. ↑ "Mitochondrial endogenous oxidative damage has been overestimated". FASEB Journal 14 (2): 355–360. February 2000. doi:10.1096/fasebj.14.2.355. PMID 10657991. 
  73. ↑ "Repair of 8-oxoG is slower in endogenous nuclear genes than in mitochondrial DNA and is without strand bias". DNA Repair 1 (4): 261–273. April 2002. doi:10.1016/S1568-7864(02)00003-4. PMID 12509245. https://zenodo.org/record/1260266. Retrieved 30 June 2019. 
  74. ↑ "[Proteins associated with mitochondrial DNA protect it against the action of X-rays and hydrogen peroxide]" (in ru). Biofizika 51 (4): 692–697. 2006. PMID 16909848. 
  75. ↑ "The maintenance of mitochondrial DNA integrity--critical analysis and update". Cold Spring Harbor Perspectives in Biology 5 (5): a012641. May 2013. doi:10.1101/cshperspect.a012641. PMID 23637283. 
  76. ↑ "Mutation". Encyclopedia of Earth. Washington DC: National Council for Science and the Environment. 2010. http://www.eoearth.org/article/Mutation?topic=49496. Retrieved 18 April 2011. 
  77. ↑ "Mitochondrial DNA and aging". Clinical Science 107 (4): 355–364. October 2004. doi:10.1042/CS20040148. PMID 15279618. 
  78. ↑ "Mitochondrial DNA disease and developmental implications for reproductive strategies". Molecular Human Reproduction 21 (1): 11–22. January 2015. doi:10.1093/molehr/gau090. PMID 25425607. 
  79. ↑ "MtDNA segregation in heteroplasmic tissues is common in vivo and modulated by haplotype differences and developmental stage". Cell Reports 7 (6): 2031–2041. June 2014. doi:10.1016/j.celrep.2014.05.020. PMID 24910436. 
  80. ↑ 80.0 80.1 "Mitochondrial DNA mutations in human disease". Nature Reviews. Genetics 6 (5): 389–402. May 2005. doi:10.1038/nrg1606. PMID 15861210. 
  81. ↑ "Mitochondrial disorders of the nuclear genome". Acta Myologica 28 (1): 16–23. July 2009. PMID 19772191. 
  82. ↑ "3.4 kb mitochondrial genome deletion serves as a surrogate predictive biomarker for prostate cancer in histopathologically benign biopsy cores". Canadian Urological Association Journal 4 (5): E118–E122. October 2010. doi:10.5489/cuaj.932. PMID 20944788. 
  83. ↑ "Accurate prediction of repeat prostate biopsy outcomes by a mitochondrial DNA deletion assay". Prostate Cancer and Prostatic Diseases 13 (2): 126–131. June 2010. doi:10.1038/pcan.2009.64. PMID 20084081. 
  84. ↑ "Measurement of Plasma Cell-Free Mitochondrial Tumor DNA Improves Detection of Glioblastoma in Patient-Derived Orthotopic Xenograft Models". Cancer Research 79 (1): 220–230. January 2019. doi:10.1158/0008-5472.CAN-18-0074. PMID 30389699. PMC 6753020. https://www.repository.cam.ac.uk/handle/1810/286401. Retrieved 24 September 2019. 
  85. ↑ The Mitochondrial Free Radical Theory of Aging. Landes Bioscience. 1999. ISBN 978-1-57059-564-6. http://www.sens.org/files/pdf/MiFRA-06.pdf. Retrieved 1 May 2016. [page needed]
  86. ↑ "The naked mole-rat response to oxidative stress: just deal with it". Antioxidants & Redox Signaling 19 (12): 1388–1399. October 2013. doi:10.1089/ars.2012.4911. PMID 23025341. 
  87. ↑ "Oxidative damage and mitochondrial decay in aging". Proceedings of the National Academy of Sciences of the United States of America 91 (23): 10771–10778. November 1994. doi:10.1073/pnas.91.23.10771. PMID 7971961. Bibcode: 1994PNAS...9110771S. 
  88. ↑ "Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production". Proceedings of the National Academy of Sciences of the United States of America 102 (50): 17993–17998. December 2005. doi:10.1073/pnas.0508886102. PMID 16332961. Bibcode: 2005PNAS..10217993T. 
  89. ↑ "Mitochondrially encoded methionine is inversely related to longevity in mammals". Aging Cell 10 (2): 198–207. April 2011. doi:10.1111/j.1474-9726.2010.00657.x. PMID 21108730. 
  90. ↑ "Improved health-span and lifespan in mtDNA mutator mice treated with the mitochondrially targeted antioxidant SkQ1". Aging 9 (2): 315–339. February 2017. doi:10.18632/aging.101174. PMID 28209927. 
  91. ↑ "Functional foods, herbs and nutraceuticals: towards biochemical mechanisms of healthy aging". Biogerontology 5 (5): 275–289. 2004. doi:10.1007/s10522-004-2566-z. PMID 15547316. 
  92. ↑ "Gene therapy for the treatment of mitochondrial DNA disorders". Expert Opinion on Biological Therapy 5 (2): 183–194. February 2005. doi:10.1517/14712598.5.2.183. PMID 15757380. 
  93. ↑ "Antioxidant supplements to prevent mortality". JAMA 310 (11): 1178–1179. September 2013. doi:10.1001/jama.2013.277028. PMID 24045742. 
  94. ↑ "Dietary restriction modulates mitochondrial DNA damage and oxylipin profile in aged rats". The FEBS Journal 289 (18): 5697–5713. September 2022. doi:10.1111/febs.16451. PMID 35373508. https://febs.onlinelibrary.wiley.com/doi/10.1111/febs.16451. Retrieved 11 May 2022. 
  95. ↑ "Increased oxidative damage in nuclear and mitochondrial DNA in Alzheimer's disease". Journal of Neurochemistry 93 (4): 953–962. May 2005. doi:10.1111/j.1471-4159.2005.03053.x. PMID 15857398. 
  96. ↑ "Neuronal failure in Alzheimer's disease: a view through the oxidative stress looking-glass". Neuroscience Bulletin 30 (2): 243–252. April 2014. doi:10.1007/s12264-013-1424-x. PMID 24733654. 
  97. ↑ "Base excision DNA repair levels in mitochondrial lysates of Alzheimer's disease". Neurobiology of Aging 35 (6): 1293–1300. June 2014. doi:10.1016/j.neurobiolaging.2014.01.004. PMID 24485507. 
  98. ↑ "Oxidative Stress in Neurodegenerative Diseases: From Molecular Mechanisms to Clinical Applications". Oxidative Medicine and Cellular Longevity 2017: 2525967. 2017. doi:10.1155/2017/2525967. PMID 28785371. 
  99. ↑ "Role of oxidative DNA damage in mitochondrial dysfunction and Huntington's disease pathogenesis". Free Radical Biology & Medicine 62: 102–110. September 2013. doi:10.1016/j.freeradbiomed.2013.04.017. PMID 23602907. 
  100. ↑ "Impairment of mitochondrial DNA repair enzymes against accumulation of 8-oxo-guanine in the spinal motor neurons of amyotrophic lateral sclerosis". Acta Neuropathologica 103 (4): 408–414. April 2002. doi:10.1007/s00401-001-0480-x. PMID 11904761. 
  101. ↑ "Mitochondrial genome anatomy and species-specific lifespan". Rejuvenation Research 9 (2): 223–226. 2006. doi:10.1089/rej.2006.9.223. PMID 16706648. 
  102. ↑ 102.0 102.1 "Do mitochondrial DNA and metabolic rate complement each other in determination of the mammalian maximum longevity?". Rejuvenation Research 11 (2): 409–417. April 2008. doi:10.1089/rej.2008.0676. PMID 18442324. 
  103. ↑ "Telomere length and body temperature-independent determinants of mammalian longevity?". Frontiers in Genetics 4 (111): 111. 2013. doi:10.3389/fgene.2013.00111. PMID 23781235. 
  104. ↑ "MitoAge: a database for comparative analysis of mitochondrial DNA, with a special focus on animal longevity". Nucleic Acids Research 44 (D1): D1262–D1265. January 2016. doi:10.1093/nar/gkv1187. PMID 26590258. 
  105. ↑ "A mitochondria-specific mutational signature of aging: increased rate of A > G substitutions on the heavy strand". Nucleic Acids Research 50 (18): 10264–10277. October 2022. doi:10.1093/nar/gkac779. PMID 36130228. 
  106. ↑ "Mitochondrial DNA deletions are associated with non-B DNA conformations". Nucleic Acids Research 40 (16): 7606–7621. September 2012. doi:10.1093/nar/gks500. PMID 22661583. 
  107. ↑ "An appraisal of human mitochondrial DNA instability: new insights into the role of non-canonical DNA structures and sequence motifs". PLOS ONE 8 (3): e59907. 2013. doi:10.1371/journal.pone.0059907. PMID 23555828. Bibcode: 2013PLoSO...859907O. 
  108. ↑ "Rapid evolution of animal mitochondrial DNA". Proceedings of the National Academy of Sciences of the United States of America 76 (4): 1967–1971. April 1979. doi:10.1073/pnas.76.4.1967. PMID 109836. Bibcode: 1979PNAS...76.1967B. 
  109. ↑ Forensic DNA typing : biology, technology, and genetics of STR markers (2nd ed.). Amsterdam: Elsevier Academic Press. 2005. pp. 241–242, 246, 258–259. ISBN 0-12-147952-8. 
  110. ↑ "Mitochondrial DNA in forensic use". Emerging Topics in Life Sciences 5 (3): 415–426. September 2021. doi:10.1042/ETLS20210204. PMID 34374411. 
  111. ↑ "Mitochondrial DNA: State of Tennessee v. Paul Ware". Profiles in DNA 1 (3): 6–7. 1998. http://www.promega.ca/~/media/files/resources/profiles%20in%20dna/103/mitochondrial%20dna%20state%20of%20tennessee%20v%20paul%20ware.pdf. Retrieved 21 October 2013. 
  112. ↑ [1] Court case name listed in the appeal.[full citation needed] Retrieved 17 April 2015.
  113. ↑ [2] [self-published source?] Defense lawyer. Retrieved 17 April 2015.
  114. ↑ "DNA Tests Got Rorrer Life in Jail". The Morning Call. 11 March 1998. 
  115. ↑ "Forensic files. a woman scorned Episode 55 Episode 55" (in en), Courtroom Television Network (Medstar Television), 2000, OCLC 456260156 
  116. ↑ "Judge allows DNA in Samantha Runnion case". 18 February 2005. http://www.nctimes.com/articles/2005/02/18/news/californian/lake_elsinore/22_48_212_17_05.txt. 
  117. ↑ "Canine DNA Admitted In California Murder Case". Pit Bulletin Legal News. 5 December 2013. http://legal.pblnn.com/pit-bulletin-legal-news-radio/97-disclaimer. 
  118. ↑ "Richard III: DNA confirms twisted bones belong to king". The Guardian. 4 February 2013. https://www.theguardian.com/science/2013/feb/04/richard-iii-dna-bones-king. 
  119. ↑ "A complete sequence of the mitochondrial genome of the western lowland gorilla". Molecular Biology and Evolution 13 (5): 691–698. May 1996. doi:10.1093/oxfordjournals.molbev.a025630. PMID 8676744. https://academic.oup.com/mbe/article/13/5/691/1083040. Retrieved 3 February 2020. 
  120. ↑ "Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes". Nature 611 (7934): 105–114. November 2022. doi:10.1038/s41586-022-05288-7. PMID 36198798. Bibcode: 2022Natur.611..105W. 
  121. ↑ "Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes". Nature 611 (7934): 105–114. November 2022. doi:10.1038/s41586-022-05288-7. PMID 36198798. Bibcode: 2022Natur.611..105W. 
  122. ↑ "Intramitochondrial Fibers with DNA Characteristics". The Journal of Cell Biology 19 (3): 593–611. December 1963. doi:10.1083/jcb.19.3.593. PMID 14086138. 
  123. ↑ "Deoxyribonucleic acid associated with yeast mitochondria". Biochemical and Biophysical Research Communications 15 (2): 127–132. March 1964. doi:10.1016/0006-291X(64)90311-0. PMID 26410904. 
  124. ↑ "AmtDB: a database of ancient human mitochondrial genomes". Nucleic Acids Research 47 (D1): D29–D32. January 2019. doi:10.1093/nar/gky843. PMID 30247677. 
  125. ↑ "InterMitoBase: an annotated database and analysis platform of protein-protein interactions for human mitochondria". BMC Genomics 12: 335. June 2011. doi:10.1186/1471-2164-12-335. PMID 21718467. 
  126. ↑ "MitoBreak: the mitochondrial DNA breakpoints database". Nucleic Acids Research 42 (Database issue): D1261–D1268. January 2014. doi:10.1093/nar/gkt982. PMID 24170808. 
  127. ↑ "MitoFish and MitoAnnotator: a mitochondrial genome database of fish with an accurate and automatic annotation pipeline". Molecular Biology and Evolution 30 (11): 2531–2540. November 2013. doi:10.1093/molbev/mst141. PMID 23955518. 
  128. ↑ "Establishment of a mitochondrial DNA sequence database for the identification of fish species commercially available in South Africa". Molecular Ecology Resources 11 (6): 979–991. November 2011. doi:10.1111/j.1755-0998.2011.03039.x. PMID 21689383. 
  129. ↑ "Mitome: dynamic and interactive database for comparative mitochondrial genomics in metazoan animals". Nucleic Acids Research 36 (Database issue): D938–D942. January 2008. doi:10.1093/nar/gkm763. PMID 17940090. 
  130. ↑ "MitoRes: a resource of nuclear-encoded mitochondrial genes and their products in Metazoa". BMC Bioinformatics 7: 36. January 2006. doi:10.1186/1471-2105-7-36. PMID 16433928. 
  131. ↑ "MitoSatPlant: mitochondrial microsatellites database of viridiplantae". Mitochondrion 19 (Pt B): 334–337. November 2014. doi:10.1016/j.mito.2014.02.002. PMID 24561221. 
  132. ↑ "MitoZoa 2.0: a database resource and search tools for comparative and evolutionary analyses of mitochondrial genomes in Metazoa". Nucleic Acids Research 40 (Database issue): D1168–D1172. January 2012. doi:10.1093/nar/gkr1144. PMID 22123747. 
  133. ↑ "Mothers can influence offspring's height, lifespan and disease risk through mitochondria" (in en). phys.org. https://phys.org/news/2021-05-mothers-offspring-height-lifespan-disease.html. 
  134. ↑ "An atlas of mitochondrial DNA genotype-phenotype associations in the UK Biobank". Nature Genetics 53 (7): 982–993. July 2021. doi:10.1038/s41588-021-00868-1. PMID 34002094. 

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