2011
DOI: 10.1007/s10863-011-9329-8
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The role of mitochondrial DNA damage in the citotoxicity of reactive oxygen species

Abstract: Mitochondria contain their own genome, a small circular molecule of around 16.5 kbases. The mitochondrial DNA (mtDNA) encodes for only 13 polypeptides, but its integrity is essential for mitochondrial function, as all 13 proteins are regulatory subunits of the oxidative phosphorylation complexes. Nonetheless, the mtDNA is physically associated with the inner mitochondrial membrane, where the majority of the cellular reactive oxygen species are generated. In fact, the mitochondrial DNA accumulates high levels o… Show more

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Cited by 42 publications
(35 citation statements)
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“…Basically, ROS can oxidize amino acids cysteine and methionine, resulting in the production of dithiol and methionine sulfoxide crosslinks, respectively [66]. Moreover, reactive species also can cause protein modification by nitration of tyrosine and by nitrosation of amino acids with thiol group.…”
Section: Protein Adductsmentioning
confidence: 99%
“…Basically, ROS can oxidize amino acids cysteine and methionine, resulting in the production of dithiol and methionine sulfoxide crosslinks, respectively [66]. Moreover, reactive species also can cause protein modification by nitration of tyrosine and by nitrosation of amino acids with thiol group.…”
Section: Protein Adductsmentioning
confidence: 99%
“…When the mitochondrial generation of ROS exceeds its antioxidant capacity, mitochondrial proteins, lipids and nucleic acids become targets of oxidation. The oxidation of mitochondrial membrane proteins leads to mitochondrial permeability transition which can contribute to the accumulation of oxidative damage in mitochondria and subsequent DNA damage (Costa et al, 2011). ROS can be produced from endogenous sources of mitochondria, peroxisomes and inflammatory cell activation, and exogenous sources including environmental agents, pharmaceuticals and industrial chemicals.…”
Section: Dna Damagementioning
confidence: 99%
“…One reason for this shortcoming is that the requirements for in vitro growth are not well characterized due to lack of knowledge regarding activation of primordial and development of primary follicles compared to development of follicles in later stages [11]. In addition, it is known that during in vitro culture of preantral follicles, there is an increase production of reactive oxygen species: ROS [12], which can affect growth, survival and consequently can lead to cell death [13]. In this context, at the present time, there is an increase interest in natural products (medicinal plants) that prevent oxidative damages caused by the ROS and as a result may contribute to promote the activation, survival, growth of preantral follicles in vitro enclosed in ovarian tissue.…”
mentioning
confidence: 99%