Редактирование: OGG1

N-glycosylase/DNA lyase [Includes: 8-oxoguanine DNA glycosylase (EC 3.2.2.-); DNA-(apurinic or apyrimidinic site) lyase (EC 4.2.99.18) (AP lyase)] [MMH] [MUTM] [OGH1]

==Publications==

{{medline-entry
|title=Impairment of Pol β-related DNA Base-excision Repair Leads to Ovarian Aging in Mice.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/33223510
|abstract=The mechanism underlying the association between age and depletion of the human ovarian follicle reserves remains uncertain. Many identified that impaired DNA polymerase β (Pol β)-mediated DNA base-excision repair (BER) drives to mouse oocyte aging. With aging, DNA lesions accumulate in primordial follicles. However, the expression of most DNA BER genes, including APE1, [[OGG1]], [[XRCC1]], Ligase I, Ligase α, [[PCNA]] and [[FEN1]], remains unchanged during aging in mouse oocytes. Also, the reproductive capacity of Pol β /- heterozygote mice was impaired, and the primordial follicle counts were lower than that of wild type (wt) mice. The DNA lesions of heterozygous mice increased. Moreover, the Pol β knockdown leads to increased DNA damage in oocytes and decreased survival rate of oocytes. Oocytes over-expressing Pol β showed that the vitality of senescent cells enhancesis significantly. Furthermore, serum concentrations of anti-Müllerian hormone (AMH) indicated that the ovarian reserves of young mice with Pol β germline mutations were lower than those in wt. These data show that Pol β-related DNA BER efficiency is a major factor governing oocyte aging in mice.

|keywords=* BER
* Pol β
* menopause
* oocytes
* ovarian aging
|full-text-url=https://sci-hub.do/10.18632/aging.104123
}}
{{medline-entry
|title=[[HDAC1]] modulates [[OGG1]]-initiated oxidative DNA damage repair in the aging brain and Alzheimer's disease.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/32424276
|abstract=DNA damage contributes to brain aging and neurodegenerative diseases. However, the factors stimulating DNA repair to stave off functional decline remain obscure. We show that [[HDAC1]] modulates [[OGG1]]-initated 8-oxoguanine (8-oxoG) repair in the brain. [[HDAC1]]-deficient mice display age-associated DNA damage accumulation and cognitive impairment. [[HDAC1]] stimulates [[OGG1]], a DNA glycosylase known to remove 8-oxoG lesions that are associated with transcriptional repression. [[HDAC1]] deficiency causes impaired [[OGG1]] activity, 8-oxoG accumulation at the promoters of genes critical for brain function, and transcriptional repression. Moreover, we observe elevated 8-oxoG along with reduced [[HDAC1]] activity and downregulation of a similar gene set in the 5XFAD mouse model of Alzheimer's disease. Notably, pharmacological activation of [[HDAC1]] alleviates the deleterious effects of 8-oxoG in aged wild-type and 5XFAD mice. Our work uncovers important roles for [[HDAC1]] in 8-oxoG repair and highlights the therapeutic potential of [[HDAC1]] activation to counter functional decline in brain aging and neurodegeneration.
|mesh-terms=* Acetylation
* Aging
* Alzheimer Disease
* Animals
* Astrocytes
* Base Sequence
* Benzophenones
* Brain
* Cognition
* Cognition Disorders
* DNA Damage
* DNA Glycosylases
* Down-Regulation
* Gene Ontology
* Guanine
* Histone Deacetylase 1
* Memory
* Mice, Inbred C57BL
* Mice, Knockout
* Neurons
* Oxidative Stress
* Promoter Regions, Genetic

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235043
}}
{{medline-entry
|title=Advanced Age Is Associated with Iron Dyshomeostasis and Mitochondrial DNA Damage in Human Skeletal Muscle.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/31783583
|abstract=Whether disruption of iron metabolism is implicated in human muscle aging is presently unclear. We explored the relationship among iron metabolism, muscle mitochondrial homeostasis, inflammation, and physical function in older adults and young controls. Eleven young and 23 older men and women were included. Older adults were classified into high-functioning (HF) and low-functioning (LF) groups according to their Short Physical Performance Battery score. Vastus lateralis muscle biopsies were assayed for total iron content, expression of 8-oxoguanine and DNA glycosylase ([[OGG1]]), 3-nitrotyrosine (3-NT) levels, and mitochondrial DNA (mtDNA) content and damage. Circulating ferritin and hepcidin levels were also quantified. Muscle iron levels were greater in the old group. Protein expression of transferrin receptor 1, Zrt-Irt-like protein (ZIP) 8, and ZIP14 were lower in old participants. Circulating levels of ferritin, hepcidin, interleukin 6 ([[IL6]]), and C-reactive protein were higher in the old group. Old participants showed lower mtDNA content and greater mtDNA damage. [[OGG1]] protein expression declined with age, whereas 3-NT levels were greater in old participants. Finally, a negative correlation was determined between ZIP14 expression and circulating [[IL6]] levels in LF older adults. None of assayed parameters differed between HF and LF participants. Our findings suggest that muscle iron homeostasis is altered in old age, which might contribute to loss of mtDNA stability. Muscle iron metabolism may therefore represent a target for interventions against muscle aging.
|mesh-terms=* Adult
* Aged
* Aged, 80 and over
* Aging
* DNA, Mitochondrial
* Female
* Homeostasis
* Humans
* Inflammation
* Iron
* Male
* Mitochondria, Muscle
* Quadriceps Muscle
* Young Adult
|keywords=* ZIP
* ferritin
* hepcidin
* inflammation
* iron overload
* mitochondrial dysfunction
* mtDNA
* muscle aging
* physical performance
* transferrin
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953082
}}
{{medline-entry
|title=8-Oxoguanine accumulation in aged female brain impairs neurogenesis in the dentate gyrus and major island of Calleja, causing sexually dimorphic phenotypes.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/31026482
|abstract=In mammals, including humans, MTH1 with 8-oxo-dGTPase and [[OGG1]] with 8-oxoguanine DNA glycosylase minimize 8-oxoguanine accumulation in genomic DNA. We investigated age-related alterations in behavior, 8-oxoguanine levels, and neurogenesis in the brains of Mth1/Ogg1-double knockout (TO-DKO), Ogg1-knockout, and human MTH1-transgenic (hMTH1-Tg) mice. Spontaneous locomotor activity was significantly decreased in wild-type mice with age, and females consistently exhibited higher locomotor activity than males. This decrease was significantly suppressed in female but not male TO-DKO mice and markedly enhanced in female hMTH1-Tg mice. Long-term memory retrieval was impaired in middle-aged female TO-DKO mice. 8-Oxoguanine accumulation significantly increased in nuclear DNA, particularly in the dentate gyrus (DG), subventricular zone (SVZ) and major island of Calleja (ICjM) in middle-aged female TO-DKO mice. In middle-aged female TO-DKO mice, neurogenesis was severely impaired in SVZ and DG, accompanied by ICjM and DG atrophy. Conversely, expression of hMTH1 efficiently suppressed 8-oxoguanine accumulation in both SVZ and DG with hypertrophy of ICjM. These findings indicate that newborn neurons from SVZ maintain ICjM in the adult brain, and increased accumulation of 8-oxoguanine in nuclear DNA of neural progenitors in females is caused by 8-oxo-dGTP incorporation during proliferation, causing depletion of neural progenitors, altered behavior, and cognitive function changes with age.
|mesh-terms=* Aging
* Animals
* Cell Proliferation
* DNA Repair Enzymes
* Dentate Gyrus
* Female
* Islands of Calleja
* Mice, Transgenic
* Neurogenesis
* Neurons
* Phenotype
* Phosphoric Monoester Hydrolases
* Sex Characteristics
|keywords=* 8-Oxoguanine
* Adult neurogenesis
* Cognitive impairment
* Dopamine receptor D3
* Major island of Calleja
* Spontaneous locomotion
|full-text-url=https://sci-hub.do/10.1016/j.pneurobio.2019.04.002
}}
{{medline-entry
|title=Sirt3 mediates the protective effect of hydrogen in inhibiting ROS-induced retinal senescence.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30735837
|abstract=Hydrogen possesses antioxidative effects and cures numerous types of ophthalmopathy, but the mechanism of hydrogen on ROS-induced retinal senescence remains elusive. In this study, retinal morphology revealed that hydrogen reduced the number and size of vitreous black deposits in Bruch's membrane in NaIO3 mice. Hydrogen also reduced ROS levels in the retina as assessed by DHE staining. Moreover, this result was consistent with the downregulation of expression of the oxidative stress hallmark [[OGG1]]. These findings suggested that hydrogen can reduce retinal oxidative stress induced by NaIO3, and this result was further verified using the antioxidant ALCAR. Mechanistic analysis revealed that hydrogen significantly inhibited the downregulation of Sirt3 expression, and this notion was confirmed using AICAR, which restores Sirt3 expression and activity. Moreover, hydrogen reduced the expression of p53, p21 and p16 and the number of blue-green precipitations in the retinas of NaIO3 mice as assessed by SA-β-gal staining. We also found that hydrogen decreased the expression of the DNA damage-related protein [[ATM]], cyclinD1 and NF-κB but increased the expression of the DNA repair-related protein [[HMGB1]], suggesting that hydrogen inhibits senescence in retinas of NaIO3 mice. Additionally, OCT examination revealed that hydrogen suppressed retinal high reflex formation significantly and prevented the retina from thinning. This result was supported by [[ERG]] assays that demonstrated that hydrogen prevented the reduction in a- and b-wave amplitude induced by NaIO3 in mice. Thus, our data suggest that hydrogen may inhibit retinal senescence by suppressing the downregulation of Sirt3 expression through reduced oxidative stress reactions.
|mesh-terms=* Acetylcarnitine
* Aging
* Animals
* Antioxidants
* Ataxia Telangiectasia Mutated Proteins
* Cyclin D1
* DNA Damage
* Gene Expression Regulation
* HMGB1 Protein
* Humans
* Hydrogen
* Iodates
* Mice
* Oxidative Stress
* Reactive Oxygen Species
* Retina
* Retinal Degeneration
* Sirtuin 3
|keywords=* DNA repair
* Hydrogen
* Retinal oxidative stress injury
* Senescence
* Sirt3
|full-text-url=https://sci-hub.do/10.1016/j.freeradbiomed.2019.02.005
}}
{{medline-entry
|title=[Protective effect of Wuzi Yanzong recipe on testicular DNA oxidative damage in natural ageing rats].
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30111059
|abstract=To study the protective effects of Wuzi Yanzong recipe on DNA oxidative damage of testis germ cells in natural ageing rats based on Nrf2/HO-1 signaling pathway and base excision repair (BER). In the study, 16-month-old SPF grade male SD rats were randomly divided into three groups, namely ageing model group, and low and high-dose Wuzi Yanzong recipe groups (WZ, 1, 4 g·kg⁻¹). In addition, 2-month-old SD rats were used as adult control group (10 rats in each group). The ageing model group and the adult control group were fed with normal diet for 4 months. WZ groups were given medicated feed for 4 months. After fasting for 12 hours, the rats were put to death. Then, the testes were immediately removed. The vitality of superoxide dismutase (SOD) and malondialdehyde (MDA) content in testis were detected by xanthine oxidase method and thiobarbituric acid (TBA) method. The levels of Nrf2 and 8-OHdG were detected by immunofluorescence. The protein expression levels of Nrf2, HO-1, [[NQO1]], APE1, [[OGG1]] and [[XRCC1]] were detected by Western blot. Compared with the ageing model group, WZ significantly increased the SOD vitality and decreased MDA content of testis. In addition, immunofluorescence results showed that WZ significantly attenuated testicular DNA oxidative damage and improved antioxidant capacity. Such changes were accompanied by the down-regulation of DNA oxidative damage response protein 8-OHdG levels and the up-regulation of Nrf2 levels. Moreover, Western blot results showed that WZ significantly increased the protein expression levels of Nrf2, HO-1 and [[NQO1]] of the testis germ cells, when compared with ageing model group. In parallel, the protein expression levels of APE1, [[OGG1]] and [[XRCC1]] were significantly decreased. In conclusion, WZ improves ageing-related DNA oxidative damage via Nrf2/HO-1 and BER pathways.
|mesh-terms=* Aging
* Animals
* DNA
* Drugs, Chinese Herbal
* Male
* NF-E2-Related Factor 2
* Oxidative Stress
* Rats
* Rats, Sprague-Dawley
* Testis
|keywords=*  DNA oxidative damage 
*  Nrf2/HO-1 signaling pathway 
*  Wuzi Yanzong recipe 
*  ageing 
*  base excision repair(BER) 
*  testis 
|full-text-url=https://sci-hub.do/10.19540/j.cnki.cjcmm.20180408.005
}}
{{medline-entry
|title=The replicative senescent mesenchymal stem / stromal cells defect in DNA damage response and anti-oxidative capacity.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30008586
|abstract=Replicative senescence and potential malignant transformation are great limitations in the clinical application of bone marrow-derived mesenchymal stem / stromal cells (MSCs). An abnormal DNA damage response may result in genomic instability, which is an integral component of aging and tumorigenesis. However, the effect of aging on the DNA damage response in MSCs is currently unknown. In the present study, we evaluated the DNA damage response induced by oxidative stress and DNA double-strand breaks in human bone marrow-derived MSCs. After long-term cell culture, replicative senescent MSCs (sMSCs) were characterized by a poor proliferation rate, high senescence-associated β-galactosidase activity, and enhanced expression of P53 and P16. Features of the DNA damage response in these sMSCs were then compared with those from early-passage MSCs. The sMSCs were more sensitive to hydrogen peroxide and bleomycin treatment with respect to cell viability and apoptosis induction. Combined with the comet assay, γH2AX foci characterization and reactive oxygen species detection were used to demonstrate that the antioxidant and DNA repair ability of sMSCs are attenuated. This result could be explained, at least in part, by the downregulation of anti-oxidation and DNA repair genes, including Cu/Zn-SOD, GPX, [[CAT]], [[OGG1]], [[XRCC1]], Ku70, [[BRCA2]] and [[XRCC4]]. In conclusion, MSCs aging is associated with a reduction in the DNA repair and anti-oxidative capacity.
|mesh-terms=* Cell Proliferation
* Cells, Cultured
* Cellular Senescence
* DNA Damage
* DNA Repair
* DNA-Binding Proteins
* Gene Expression Regulation
* Humans
* Mesenchymal Stem Cells
* Oxidative Stress
|keywords=* DNA damage response
* DNA double-strand breaks
* Replicative senescence
* mesenchymal stem cells
* oxidative stress
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036081
}}
{{medline-entry
|title=DNA damage and telomere length shortening in the peripheral blood leukocytes of 20 years SM-exposed veterans.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29803135
|abstract=Sulfur mustard (SM) is a vesicant chemical warfare agent, and a very potent alkylating agent. SM exerts its cytotoxicity via direct alkylation of biomacromolecules, and overproduction of reactive oxygen species (ROS). Previous studies have shown that SM-induced oxidative stress has adverse effects on antioxidant defense system, and damages lipids and proteins. The aim of this study was to investigate the effect of SM-induced oxidative stress on DNA damage, and cellular senescence in SM-exposed victims. For this purpose, MDA levels as a measure of oxidative stress in the serum, 8-oxo-dG content of the genomic DNA, and [[OGG1]] expression as two biomarkers of oxidative DNA damage, as well as, telomere length, and p16  expression as two biomarkers of cellular senescence were measured in the peripheral blood leukocytes of 215 males who were exposed to SM 20 to 25 years ago, and 53 unexposed healthy males as the control group. Our results indicated that the levels of 8-oxo-dG, and [[OGG1]] mRNA expression were significantly higher in SM-exposed individuals. Furthermore, a significant increase in the expression of p16  was observed in SM-exposed patients, and leukocyte telomere length (LTL) was also significantly shorter in severe/very severe cases of SM-exposed patients when compared with unexposed controls. In conclusion, our data indicate that oxidative DNA damage is higher in SM-exposed patients, and their immune system has subjected to cellular senescence.
|mesh-terms=* 8-Hydroxy-2'-Deoxyguanosine
* Adult
* Cellular Senescence
* Chemical Warfare Agents
* Cyclin-Dependent Kinase Inhibitor p16
* DNA Damage
* DNA Glycosylases
* Deoxyguanosine
* Humans
* Iran
* Leukocytes, Mononuclear
* Middle Aged
* Mustard Gas
* Oxidative Stress
* Reactive Oxygen Species
* Telomere
* Time Factors
* Veterans
|keywords=* Cellular senescence
* Oxidative DNA damage
* Sulfur mustard
|full-text-url=https://sci-hub.do/10.1016/j.intimp.2018.05.008
}}
{{medline-entry
|title="What makes some rats live so long?" The mitochondrial contribution to longevity through balance of mitochondrial dynamics and mtDNA content.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27620821
|abstract=Extremely interesting for aging research are those individuals able to reach older ages still with functions similar to those of younger counterparts. We examined liver samples from ad libitum-fed old (28-month-old, AL-28) and ad libitum-fed very old (32-month-old, AL-32) rats for a number of markers, relevant for mitochondrial functionality and mitochondrial DNA (mtDNA) content. As for the mtDNA content and the protein amounts of the citrate synthase and the antioxidant peroxiredoxin III there were no significant changes in the AL-32 animals. No significant longevity-related change was found for [[TFAM]] amount, but a 50% reduction in the amount of the Lon protease, responsible for turnover of [[TFAM]] inside mitochondria, characterized the AL-32 rats. No longevity-related change was observed also for the amounts of the mtDNA repair enzymes [[OGG1]] and APE1, whereas the intra-mitochondrial amount of the cytochrome c protein showed a 50% increase in the AL-32 rats, indicating a likely reduced initiation of the intrinsic apoptotic pathway. Totally unexpected was the doubling of two proteins, very relevant for mitochondrial dynamics, namely [[MFN2]] and DRP1, in the AL-32 rats. This prompted us to the calculation of all individual fusion indexes that grouped together in the AL-32 rats, while in the AL-28 animals were very different. We found a strong positive correlation between the fusion indexes and the respective mtDNA contents in two AL-28 and four AL-32 rats. This supports the idea that the limited prevalence of fusion above a still active fission should have ensured a functional mitochondrial network and should have led to a quite narrow range of high mtDNA contents, likely the best-suitable for extended longevity. Our findings strongly suggest that, among the multiple causes leading to the longevity of the AL-32 rats, the maintenance of an adult-like balance of mitochondrial dynamics seems to be very relevant for the regulation of mtDNA content and functionality.
|mesh-terms=* Aging
* Animals
* DNA Repair
* DNA, Mitochondrial
* Longevity
* Male
* Mitochondria
* Mitochondrial Dynamics
* Rats
* Rats, Inbred F344
* Transcription Factors
|keywords=* Aged liver mitochondria
* Fusion index correlation with mtDNA content
* Long-living rats
* Mitochondrial dynamics
* mtDNA and related proteins
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5922457
}}
{{medline-entry
|title=8-Oxoguanine DNA glycosylase1-driven DNA repair-A paradoxical role in lung aging.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27343030
|abstract=Age-associated changes in lung structure and function are some of the most important predictors of overall health, cognitive activities and longevity. Common to all aging cells is an increase in oxidatively modified DNA bases, primarily 8-oxo-7,8-dihydroguanine (8-oxoG). It is repaired via DNA base excision repair pathway driven by 8-oxoguanine DNA glycosylase-1 ([[OGG1]]-BER), whose role in aging has been the focus of many studies. This study hypothesizes that signaling and consequent gene expression during cellular response to [[OGG1]]-BER "wires" senescence/aging processes. To test [[OGG1]]-BER was mimicked by repeatedly exposing diploid lung fibroblasts cells and airways of mice to 8-oxoG base. Results showed that repeated exposures led to G1 cell cycle arrest and pre-matured senescence of cultured cells in which over 1000 genes were differentially expressed -86% of them been identical to those in naturally senesced cells. Gene ontology analysis of gene expression displayed biological processes driven by small GTPases, phosphoinositide 3-kinase and mitogen activated kinase cascades both in cultured cells and lungs. These results together, points to a new paradigm about the role of DNA damage and repair by [[OGG1]] in aging and age-associated disease processes.
|mesh-terms=* Aging
* Animals
* Cell Line
* DNA Glycosylases
* DNA Repair
* Fibroblasts
* G1 Phase Cell Cycle Checkpoints
* Humans
* Lung
* Mice
|keywords=* 8-oxoguanine
* Aging
* OGG1
* Senescence
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5177546
}}
{{medline-entry
|title=Sex-specific effects of cytotoxic chemotherapy agents cyclophosphamide and mitomycin C on gene expression, oxidative DNA damage, and epigenetic alterations in the prefrontal cortex and hippocampus - an aging connection.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27032448
|abstract=Recent research shows that chemotherapy agents can be more toxic to healthy brain cells than to the target cancer cells. They cause a range of side effects, including memory loss and cognitive dysfunction that can persist long after the completion of treatment. This condition is known as chemo brain. The molecular and cellular mechanisms of chemo brain remain obscure. Here, we analyzed the effects of two cytotoxic chemotherapy drugs-cyclophosphamide (CPP) and mitomycin C (MMC) - on transcriptomic and epigenetic changes in the murine prefrontal cortex (PFC) and hippocampal regions. We for the first time showed that CPP and MMC treatments led to profound sex- and brain region-specific alterations in gene expression profiles. Gene expression changes were most prominent in the PFC tissues of female mice 3 weeks after MMC treatment, and the gene expression response was much greater for [[MCC]] than CPP exposure. MMC exposure resulted in oxidative DNA damage, evidenced by accumulation of 8-oxo-2'-deoxyguanosine (8-oxodG) and a decrease in the level of 8-oxodG repair protein [[OGG1]] in the PFC of female animals 3 weeks after treatment. MMC treatment decreased global DNA methylation and increased DNA hydroxymethylation in the PFC tissues of female mice. The majority of the changes induced by chemotherapy in the PFC tissues of female mice resembled those that occur during the brain's aging processes. Therefore, our study suggests a link between chemotherapy-induced chemo brain and brain aging, and provides an important roadmap for future analysis.
|mesh-terms=* Animals
* Antineoplastic Agents
* Cyclophosphamide
* DNA Damage
* Epigenesis, Genetic
* Female
* Gene Expression
* Gene Expression Profiling
* Gene Expression Regulation
* Hippocampus
* Male
* Mice
* Mitomycin
* Oxidative Stress
* Prefrontal Cortex
* Sex Factors
|keywords=* DNA hydroxymethylation
* DNA methylation
* aging
* chemo brain
* chemotherapy
* epigenetics
* oxidative stress
* transcriptome
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4925823
}}
{{medline-entry
|title=[The polymorphism of DNA repair genes XPD, XRCC1, [[OGG1]], and ERCC6, life expectancy, and the inclination to smoke].
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/25731027
|abstract=The polymorphism of excision repair genes XPD Asp312Asn, XRCC1 Arg399Gln, [[OGG1]] Ser326Cys, and ERCC6 Met1097Val was analyzed by PCR-RFLP in 370 representatives of the Belarusian population of average, old, and elderly ages. Correlation analysis showed that the frequencies of wild-type homozygous combinations significantly increase with age in the group of subjects over 70 years old in the case of the interaction of two genes, XPD 312 and XRCC1399, or three genes, XPD312, XRCC1399, and ERCC6 1097. In a subgroup of the long-lived, this relationship is manifested in case of a pairwise interaction of gene XPD 312 with XRCC1 399 or ERCC6 1097, as well as an interaction of three genes, XPD 312, XRCC1 399, and ERCC6 1097. The data suggest that the optimum activity of repair processes may favor longevity. It is shown that the frequency of the Asp/Asp genotype is reduced, and the frequency of the Asn allele of the XPD 312 gene is increased in the subgroup of smokers as compared with nonsmokers, which apparently indicates an association of this gene polymorphism with an inclination to smoke. The problem requires further study.
|mesh-terms=* Adult
* Aged
* Aged, 80 and over
* DNA Glycosylases
* DNA Helicases
* DNA Repair
* DNA Repair Enzymes
* DNA-Binding Proteins
* Female
* Genetic Predisposition to Disease
* Humans
* Longevity
* Male
* Middle Aged
* Poly-ADP-Ribose Binding Proteins
* Polymorphism, Genetic
* Smoking
* X-ray Repair Cross Complementing Protein 1
* Xeroderma Pigmentosum Group D Protein


}}
{{medline-entry
|title=Altered DNA Methylation and Expression Profiles of 8-Oxoguanine DNA Glycosylase 1 in Lens Tissue from Age-related Cataract Patients.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/25310012
|abstract=Oxidative stress and DNA damage contribute to the pathogenesis of age-related cataract (ARC). Most oxidative DNA lesions are repaired via the base excision repair (BER) proteins including 8-oxoguanine DNA glycosylase 1 ([[OGG1]]). This study examined DNA methylation of CpG islands upstream of [[OGG1]] and their relation to the gene expression in lens cortex from ARC patients. The clinical case-control study consisted of 15 cortical type of ARC patients and 15 age-matched non-ARC controls who received transparent lens extraction due to vitreoretinal diseases. [[OGG1]] expression in lens cortex was analyzed by qRT-PCR and Western blot. The localization and the proportion of cells positive for [[OGG1]] were determined by immunofluorescence. Bisulfite-sequencing PCR (BSP) was performed to evaluate the methylation status of CpG islands near [[OGG1]] in DNA extracted from lens cortex. To test relationship between the methylation and the expression of the gene of interest, 5-Aza-2'-deoxycytidine (5-Aza-dC) was used to induce demethylation of cultured human lens epithelium B-3 (HLE B-3). To test the role of [[OGG1]] in the repair of cellular damage, HLE B-3 was transfected with [[OGG1]] vector, followed by ultraviolet radiation b (UVB) exposure to induce apoptosis. The mRNA and protein levels of [[OGG1]] were significantly reduced in the lens cortex of ARC. Immunofluorescence showed that the proportion of [[OGG1]]-positive cells decreased significantly in ARC cortex in comparison with the control. The CpG island in first exon of [[OGG1]] displayed hypermethylation in the DNA extracted from the lens cortex of ARC. Treatment of HLEB-3 cells with 5-Aza-dC upregulated [[OGG1]] expression. UVB-induced apoptosis was attenuated after transfection with [[OGG1]]. A reduced [[OGG1]] expression was correlated with hypermethylation of a CpG island of [[OGG1]] in lens cortex of ARC. The role of epigenetic change in [[OGG1]] gene in the susceptibility to oxidative stress induced cortical ARC is warranted to further study.
|mesh-terms=* Aging
* Apoptosis
* Blotting, Western
* Case-Control Studies
* Cataract
* Cells, Cultured
* CpG Islands
* DNA Glycosylases
* DNA Methylation
* Epithelial Cells
* Fluorescent Antibody Technique, Indirect
* Gene Expression Regulation
* Genetic Vectors
* Humans
* Lens Cortex, Crystalline
* Oxidative Stress
* RNA, Messenger
* Real-Time Polymerase Chain Reaction
* Transfection
* Ultraviolet Rays
|keywords=* 8-oxoguanine DNA glycosylase 1
* Age-related cataract
* DNA methylation
* lens cortex
* oxidative stress
|full-text-url=https://sci-hub.do/10.3109/02713683.2014.957778
}}
{{medline-entry
|title=Polymorphisms of DNA repair genes [[OGG1]] and XPD and the risk of age-related cataract in Egyptians.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/24868140
|abstract=To analyze the association of the polymorphisms of xeroderma pigmentosum complementation group D (XPD) and 8-oxoguanine glycosylase-1 ([[OGG1]]) genes with the risk of age-related cataract ([[ARC]]) in an Egyptian population. This case-control study included 150 patients with [[ARC]] and 50 controls. Genotyping of XPD Asp³¹²Asn was performed by amplification refractory mutation system PCR assay and genotyping of [[OGG1]] Ser³²⁶Cys was carried out by PCR including confronting two-pair primers. The Asn/Asn genotype of XPD gene was significantly associated with increased risk of [[ARC]] (odds ratio [OR] = 2.74, 95% confidence interval [CI] = 1.01-7.43, p = 0.04) and cortical cataract (OR = 5.06, 95% CI = 1.70-15.05, p = 0.002). The Asn³¹² allele was significantly associated with an increased risk of [[ARC]] (OR = 1.75, 95% CI 1.06-2.89, p = 0.03) and cortical cataract (OR = 2.81, 95% CI = 1.56-5.08, p<0.001). The [[OGG1]] Cys/Cys genotype frequency was significantly higher in [[ARC]] (OR = 4.13, 95% CI = 0.93-18.21, p = 0.04) and the Cys(³²⁶ allele (OR = 1.85, 95% CI = 1.07-3.20, p = 0.03). Moreover, the Cys/Cys genotype of the [[OGG1]] gene was significantly higher in cortical cataract (OR = 6.00, 95% CI = 1.24-28.99, p = 0.01) and the Cys³²⁶ allele was also significantly associated with cortical cataract (OR = 2.45, 95% CI = 1.30-4.63, p = 0.005). The results suggest that the Asn/Asn genotype and Asn³¹² allele of XPD polymorphism, as well as the Cys/Cys genotype and Cys³²⁶ allele of the [[OGG1]] polymorphism, may be associated with increased risk of the development of [[ARC]], particularly the cortical type, in the Egyptian population.
|mesh-terms=* Aged
* Aging
* Alleles
* Case-Control Studies
* Cataract
* DNA Glycosylases
* DNA Repair
* Demography
* Egypt
* Female
* Gene Frequency
* Genetic Predisposition to Disease
* Humans
* Male
* Middle Aged
* Polymorphism, Single Nucleotide
* Risk Factors
* Xeroderma Pigmentosum Group D Protein

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029483
}}
{{medline-entry
|title=Postprandial activation of p53-dependent DNA repair is modified by Mediterranean diet supplemented with coenzyme Q10 in elderly subjects.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/24158762
|abstract=Alterations in the expression levels of genes and proteins involved in oxidative stress and DNA damage response underlie the phenotypic changes associated with aging. We have investigated whether the quality of dietary fat alters postprandial gene expression and protein levels involved in p53-dependent DNA repair and whether the supplementation with Coenzyme Q10 improves this situation in an elderly population. Twenty participants were randomized to receive three isocaloric diets each for 4 weeks: Mediterranean diet supplemented with Coenzyme Q10, Mediterranean diet, saturated fatty acid-rich diet. After a 12-hour fast, volunteers consumed a breakfast with a fat composition similar to that consumed in each of the diets. Gadd45a, Gadd45b, [[OGG1]], APE-1/Ref-1, DNApolβ, and [[XPC]] gene expression and nuclear Gadd45a, APE-1/Ref-1, and DNApolβ protein levels were determined in peripheral blood mononuclear cells. Mediterranean diet and Mediterranean diet supplemented with Coenzyme Q10diets downregulated Gadd45a protein levels compared with the saturated fatty acid-rich diet. Moreover, Mediterranean diet supplemented with Coenzyme Q10diet evoked lower postprandial Gadd45a, Gadd45b, [[XPC]], DNApolβ and [[OGG1]] gene expression and lower APE-1/Ref-1 and DNApolβ protein levels than the saturated fatty acid-rich diet. Our results support a beneficial effect of Mediterranean diet and Mediterranean diet supplemented with Coenzyme Q10 on DNA damage as compared to the detrimental action of a saturated fatty acid-rich diet, which triggers the p53-dependent DNA repair machinery.
|mesh-terms=* Aged
* Aging
* Cell Cycle Proteins
* Cross-Over Studies
* DNA Glycosylases
* DNA Polymerase beta
* DNA Repair
* DNA-(Apurinic or Apyrimidinic Site) Lyase
* DNA-Binding Proteins
* Diet, Mediterranean
* Dietary Supplements
* Female
* Gene Expression
* Genes, p53
* Humans
* Leukocytes, Mononuclear
* Male
* Nuclear Proteins
* Postprandial Period
* RNA, Messenger
* Ubiquinone
|keywords=* DNA damage and repair
* Metabolism.
* Nutrition
* Oxidative stress
|full-text-url=https://sci-hub.do/10.1093/gerona/glt174
}}
{{medline-entry
|title=The senescence-accelerated mouse prone 8 as a model for oxidative stress and impaired DNA repair in the male germ line.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/23813448
|abstract=The discovery of a truncated base excision repair pathway in human spermatozoa mediated by [[OGG1]] has raised questions regarding the effect of mutations in critical DNA repair genes on the integrity of the paternal genome. The senescence-accelerated mouse prone 8 (SAMP8) is a mouse model containing a suite of naturally occurring mutations resulting in an accelerated senescence phenotype largely mediated by oxidative stress, which is further enhanced by a mutation in the Ogg1 gene, greatly reducing the ability of the enzyme to excise 8-hydroxy,2'-deoxyguanosine (8OHdG) adducts. An analysis of the reproductive phenotype of the SAMP8 males revealed a high level of DNA damage in caudal epididymal spermatozoa as measured by the alkaline Comet assay. Furthermore, these lesions were confirmed to be oxidative in nature, as demonstrated by significant increases in 8OHdG adduct formation in the SAMP8 testicular tissue (P<0.05) as well as in mature spermatozoa (P<0.001) relative to a control strain (SAMR1). Despite this high level of oxidative DNA damage in spermatozoa, reactive oxygen species generation was not elevated and motility of spermatozoa was found to be similar to that for the control strain with the exception of progressive motility, which exhibited a slight but significant decline with advancing age (P<0.05). When challenged with Fenton reagents (H2O2 and Fe2 ), the SAMP8 spermatozoa demonstrated a highly increased susceptibility to formation of 8OHdG adducts compared with the controls (P<0.001). These data highlight the role of oxidative stress and [[OGG1]]-dependent base excision repair mechanisms in defining the genetic integrity of mammalian spermatozoa.
|mesh-terms=* Aging
* Animals
* DNA Damage
* DNA Glycosylases
* DNA Repair
* Fertility
* Male
* Mice
* Models, Animal
* Oxidative Stress
* Phenotype
* Spermatogenesis
* Spermatozoa

|full-text-url=https://sci-hub.do/10.1530/REP-13-0186
}}
{{medline-entry
|title=Age-dependent guanine oxidation in DNA of different brain regions of Wistar rats and prematurely aging OXYS rats.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/23403132
|abstract=Oxidative damage to the cell, including the formation of 8-oxoG, has been regarded as a significant factor in carcinogenesis and aging. An inbred prematurely aging rat strain (OXYS) is characterized by high sensitivity to oxidative stress, lipid peroxidation, protein oxidation, DNA rearrangements, and pathological conditions paralleling several human degenerative diseases including learning and memory deterioration. We have used monoclonal antibodies against a common pre-mutagenic base lesion 8-oxoguanine (8-oxoG) and 8-oxoguanine DNA glycosylase ([[OGG1]]) in combination with indirect immunofluorescence microscopy and image analysis to follow the relative amounts and distribution of 8-oxoG and [[OGG1]] in various cells of different brain regions from OXYS and control Wistar rats. It was shown that 8-oxoG increased with age in mature neurons, nestin- and glial fibrillary acidic protein ([[GFAP]])-positive cells of hippocampus and frontal cortex in both strains of rats, with OXYS rats always displaying statistically significantly higher levels of oxidative DNA damage than Wistar rats. The relative content of 8-oxoG and [[OGG1]] in nestin- and [[GFAP]]-positive cells was higher than in mature neurons in both Wistar and OXYS rats. However, there was no significant interstrain difference in the content of [[OGG1]] for all types of cells and brain regions analyzed, and no difference in the relative content of 8-oxoG between different brain regions. Oxidation of guanine may play an important role in the development of age-associated decrease in memory and learning capability of OXYS rats. The findings are important for validation of the OXYS rat strain as a model of mammalian aging.
|mesh-terms=* Aging
* Aging, Premature
* Animals
* DNA Damage
* DNA Glycosylases
* Frontal Lobe
* Guanine
* Hippocampus
* Humans
* Intermediate Filament Proteins
* Lipid Peroxidation
* Memory
* Nerve Tissue Proteins
* Nestin
* Neurons
* Oxidative Stress
* Rats
* Rats, Wistar

|full-text-url=https://sci-hub.do/10.1016/j.bbagen.2013.01.027
}}