8-Oxoguanine causes neurodegeneration during MUTYH-mediated DNA base excision repair

scientific article

8-Oxoguanine causes neurodegeneration during MUTYH-mediated DNA base excision repair is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1172/JCI65053
P932PMC publication ID3533558
P698PubMed publication ID23143307

P2093author name stringHidetaka Yamada
Yusaku Nakabeppu
Daisuke Tsuchimoto
Kunihiko Sakumi
Nona Abolhassani
Sugako Oka
Hiroko Nomaru
Zijing Sheng
P2860cites workNUDT16 is a (deoxy)inosine diphosphatase, and its deficiency induces accumulation of single-strand breaks in nuclear DNA and growth arrestQ24306490
An oxidized purine nucleoside triphosphatase, MTH1, suppresses cell death caused by oxidative stressQ24307873
Genomic structure and chromosome location of the human mutT homologue gene MTH1 encoding 8-oxo-dGTPase for prevention of A:T to C:G transversionQ24313376
Cloning and expression of cDNA for a human enzyme that hydrolyzes 8-oxo-dGTP, a mutagenic substrate for DNA synthesisQ24318724
Spontaneous tumorigenesis in mice defective in the MTH1 gene encoding 8-oxo-dGTPaseQ24555183
Oxidants, antioxidants, and the degenerative diseases of agingQ24561734
Cloning and sequencing a human homolog (hMYH) of the Escherichia coli mutY gene whose function is required for the repair of oxidative DNA damageQ28114912
Oxidants, oxidative stress and the biology of ageingQ28131725
Expression and differential intracellular localization of two major forms of human 8-oxoguanine DNA glycosylase encoded by alternatively spliced OGG1 mRNAsQ28143253
Ogg1 knockout-associated lung tumorigenesis and its suppression by Mth1 gene disruptionQ28180293
Oxidation of the guanine nucleotide pool underlies cell death by bactericidal antibioticsQ28264943
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseasesQ28269333
Hydroxylation of deoxyguanosine at the C-8 position by ascorbic acid and other reducing agentsQ28367039
A role for oxidized DNA precursors in Huntington's disease-like striatal neurodegenerationQ28474016
Perikaryal accumulation and proteolysis of neurofilament proteins in the post-mortem rat brainQ28571322
Identification of human MutY homolog (hMYH) as a repair enzyme for 2-hydroxyadenine in DNA and detection of multiple forms of hMYH located in nuclei and mitochondriaQ28610376
Cloning and characterization of mammalian 8-hydroxyguanine-specific DNA glycosylase/apurinic, apyrimidinic lyase, a functional mutM homologueQ28610622
Microglia-mediated neurotoxicity: uncovering the molecular mechanismsQ29547835
Human APE2 protein is mostly localized in the nuclei and to some extent in the mitochondria, while nuclear APE2 is partly associated with proliferating cell nuclear antigenQ31919701
MTH1, an oxidized purine nucleoside triphosphatase, suppresses the accumulation of oxidative damage of nucleic acids in the hippocampal microglia during kainate-induced excitotoxicity.Q33233462
Replicating Huntington's disease phenotype in experimental animalsQ33749061
Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primatesQ34103541
Mutagenesis and carcinogenesis caused by the oxidation of nucleic acids.Q34512398
???Q64819937
Extrinsic connections of the basal gangliaQ34570614
Chemistry-based studies on oxidative DNA damage: formation, repair, and mutagenesisQ34772321
Human mitochondrial DNA is packaged with TFAM.Q34908739
Nuclear and mitochondrial conversations in cell death: PARP-1 and AIF signalingQ35761624
Spectrin and calpain: a 'target' and a 'sniper' in the pathology of neuronal cells.Q36180675
3-Nitropropionic acid: a mitochondrial toxin to uncover physiopathological mechanisms underlying striatal degeneration in Huntington's disease.Q36318579
Oxidative damage in nucleic acids and Parkinson's disease.Q36728710
3-Nitropropionic acid-exogenous animal neurotoxin and possible human striatal toxin.Q36934346
Base excision repair of oxidative DNA damage and association with cancer and agingQ37090426
Calpain-mediated signaling mechanisms in neuronal injury and neurodegenerationQ37237452
Programmed cell death triggered by nucleotide pool damage and its prevention by MutT homolog-1 (MTH1) with oxidized purine nucleoside triphosphataseQ37764544
DNA glycosylase encoded by MUTYH functions as a molecular switch for programmed cell death under oxidative stress to suppress tumorigenesis.Q37828633
Two distinct pathways of cell death triggered by oxidative damage to nuclear and mitochondrial DNAs.Q40026363
Microglial activation and cell death induced by the mitochondrial toxin 3-nitropropionic acid: in vitro and in vivo studiesQ40660071
Expression of 8-oxoguanine DNA glycosylase is reduced and associated with neurofibrillary tangles in Alzheimer's disease brain.Q42168961
Quantitative analysis of oxidized guanine, 8-oxoguanine, in mitochondrial DNA by immunofluorescence method.Q42455152
Basal ganglia degeneration, myelin alterations, and enzyme inhibition induced in mice by the plant toxin 3-nitropropanoic acidQ42464071
Expression of 8-oxoguanine DNA glycosylase (OGG1) in Parkinson's disease and related neurodegenerative disordersQ42477148
Antibody against single-stranded DNA useful for detecting apoptotic cells recognizes hexadeoxynucleotides with various base sequencesQ42543660
Expression of hMTH1 in the hippocampi of control and Alzheimer's diseaseQ43757877
Regulation of microglial expression of integrins by poly(ADP-ribose) polymerase-1.Q43848053
Deficiencies in mouse Myh and Ogg1 result in tumor predisposition and G to T mutations in codon 12 of the K-ras oncogene in lung tumorsQ44224012
Accumulation of 8-oxoguanine in the cellular DNA and the alteration of the OGG1 expression during ischemia-reperfusion injury in the rat kidney.Q44280605
Mutator phenotype of MUTYH-null mouse embryonic stem cells.Q44548854
Quantifiable bradykinesia, gait abnormalities and Huntington's disease-like striatal lesions in rats chronically treated with 3-nitropropionic acidQ45294402
Oxidative damage to mitochondrial DNA in Huntington's disease parietal cortexQ45299186
Mitochondrial and nuclear DNA-repair capacity of various brain regions in mouse is altered in an age-dependent manner.Q46590824
MTH1, an oxidized purine nucleoside triphosphatase, protects the dopamine neurons from oxidative damage in nucleic acids caused by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine.Q46793098
Oxidation of mitochondrial deoxynucleotide pools by exposure to sodium nitroprusside induces cell death.Q46835805
Up-regulation of hMUTYH, a DNA repair enzyme, in the mitochondria of substantia nigra in Parkinson's diseaseQ48497446
Increased oxidative damage in nuclear and mitochondrial DNA in Alzheimer's diseaseQ48910103
Antibody against single-stranded DNA detects both programmed cell death and drug-induced apoptosis.Q52220877
MUTYH-null mice are susceptible to spontaneous and oxidative stress induced intestinal tumorigenesisQ80635837
P4510describes a project that usesImageJQ1659584
P433issue12
P407language of work or nameEnglishQ1860
P921main subjectneurodegenerationQ1755122
P304page(s)4344-4361
P577publication date2012-11-12
P1433published inJournal of Clinical InvestigationQ3186904
P1476title8-Oxoguanine causes neurodegeneration during MUTYH-mediated DNA base excision repair
P478volume122

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cites work (P2860)
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