Regulation of PINK1-Parkin-mediated mitophagy
暂无分享,去创建一个
[1] S. Shimizu,et al. Paraquat Toxicity Induced by Voltage-dependent Anion Channel 1 Acts as an NADH-dependent Oxidoreductase* , 2009, The Journal of Biological Chemistry.
[2] A. Spradling,et al. clueless, a conserved Drosophila gene required for mitochondrial subcellular localization, interacts genetically with parkin , 2009, Disease Models & Mechanisms.
[3] Andrew B West,et al. Molecular pathophysiology of Parkinson's disease. , 2005, Annual review of neuroscience.
[4] David W. Miller,et al. Mitochondrial Alterations in PINK1 Deficient Cells Are Influenced by Calcineurin-Dependent Dephosphorylation of Dynamin-Related Protein 1 , 2009, PloS one.
[5] R. Takahashi,et al. Parkin Phosphorylation and Modulation of Its E3 Ubiquitin Ligase Activity* , 2005, Journal of Biological Chemistry.
[6] David S. Park,et al. BAG5 Inhibits Parkin and Enhances Dopaminergic Neuron Degeneration , 2004, Neuron.
[7] K. Lim,et al. Jcb: Report , 2022 .
[8] Fabienne C. Fiesel,et al. PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1 , 2010, Nature Cell Biology.
[9] Wei Jiang,et al. Parkin, PINK1, and DJ-1 form a ubiquitin E3 ligase complex promoting unfolded protein degradation. , 2009, The Journal of clinical investigation.
[10] A. Reichert,et al. Loss-of-Function of Human PINK1 Results in Mitochondrial Pathology and Can Be Rescued by Parkin , 2007, The Journal of Neuroscience.
[11] Atsushi Tanaka. Parkin‐mediated selective mitochondrial autophagy, mitophagy: Parkin purges damaged organelles from the vital mitochondrial network , 2010, FEBS letters.
[12] T. Hashikawa,et al. CHIP is associated with Parkin, a gene responsible for familial Parkinson's disease, and enhances its ubiquitin ligase activity. , 2002, Molecular cell.
[13] David W. Miller,et al. Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[14] A. Brice,et al. Biochemical analysis of Parkinson's disease-causing variants of Parkin, an E3 ubiquitin-protein ligase with monoubiquitylation capacity. , 2006, Human molecular genetics.
[15] R. Szargel,et al. Phosphorylation of Parkin by the Cyclin-dependent Kinase 5 at the Linker Region Modulates Its Ubiquitin-Ligase Activity and Aggregation* , 2007, Journal of Biological Chemistry.
[16] Lan Huang,et al. Quantitative analysis of global ubiquitination in HeLa cells by mass spectrometry. , 2008, Journal of proteome research.
[17] Steve D. M. Brown,et al. Dynein mutations impair autophagic clearance of aggregate-prone proteins , 2005, Nature Genetics.
[18] J. Troncoso,et al. Phosphorylation by the c-Abl protein tyrosine kinase inhibits parkin's ubiquitination and protective function , 2010, Proceedings of the National Academy of Sciences.
[19] N. Hattori,et al. PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy , 2010, The Journal of cell biology.
[20] K. Nakayama,et al. U Box Proteins as a New Family of Ubiquitin-Protein Ligases* , 2001, The Journal of Biological Chemistry.
[21] M. W. Wooten,et al. Sequestosome 1/p62 shuttles polyubiquitinated tau for proteasomal degradation , 2005, Journal of neurochemistry.
[22] Ji Zhang,et al. NIX induces mitochondrial autophagy in reticulocytes , 2008, Autophagy.
[23] Gwang Lee,et al. Molecular interaction between parkin and PINK1 in mammalian neuronal cells , 2009, Molecular and Cellular Neuroscience.
[24] R. King,et al. Differential effects of PINK1 nonsense and missense mutations on mitochondrial function and morphology , 2009, Experimental Neurology.
[25] D. Perl,et al. Lewy-body formation is an aggresome-related process: a hypothesis , 2004, The Lancet Neurology.
[26] M. Beal,et al. Mitochondrial pathology and muscle and dopaminergic neuron degeneration caused by inactivation of Drosophila Pink1 is rescued by Parkin. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[27] Takashi Uehara,et al. Nitrosative stress linked to sporadic Parkinson's disease: S-nitrosylation of parkin regulates its E3 ubiquitin ligase activity. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[28] J. McCaffery,et al. Mitochondrial Fusion Intermediates Revealed in Vitro , 2004, Science.
[29] H. Sandoval,et al. Essential role for Nix in autophagic maturation of erythroid cells , 2008, Nature.
[30] Jie Shen,et al. Loss of PINK1 causes mitochondrial functional defects and increased sensitivity to oxidative stress , 2008, Proceedings of the National Academy of Sciences.
[31] Angela C. Poole,et al. The PINK1/Parkin pathway regulates mitochondrial morphology , 2008, Proceedings of the National Academy of Sciences.
[32] N. Wood,et al. PINK1 function in health and disease , 2009, EMBO molecular medicine.
[33] Sharon Y. R. Dent,et al. HDAC6 modulates cell motility by altering the acetylation level of cortactin. , 2007, Molecular cell.
[34] Jian Feng,et al. Direct Binding with Histone Deacetylase 6 Mediates the Reversible Recruitment of Parkin to the Centrosome , 2008, The Journal of Neuroscience.
[35] William Lin,et al. Characterization of PINK1 processing, stability, and subcellular localization , 2008, Journal of neurochemistry.
[36] Alexandra Durr,et al. How much phenotypic variation can be attributed to parkin genotype? , 2003, Annals of neurology.
[37] J. M. Bravo-San Pedro,et al. Silencing DJ‐1 reveals its contribution in paraquat‐induced autophagy , 2009, Journal of neurochemistry.
[38] Reidun Torp,et al. Mitochondrial localization of the Parkinson's disease related protein DJ-1: implications for pathogenesis. , 2005, Human molecular genetics.
[39] K. Lim,et al. Familial-associated mutations differentially disrupt the solubility, localization, binding and ubiquitination properties of parkin. , 2005, Human molecular genetics.
[40] T. Hoppe,et al. A Caenorhabditis elegans Parkin mutant with altered solubility couples alpha-synuclein aggregation to proteotoxic stress. , 2005, Human molecular genetics.
[41] M. Cookson,et al. LRRK2 Modulates Vulnerability to Mitochondrial Dysfunction in Caenorhabditis elegans , 2009, The Journal of Neuroscience.
[42] R. Kopito,et al. Aggresomes, inclusion bodies and protein aggregation. , 2000, Trends in cell biology.
[43] J. Vance,et al. The Deacetylase HDAC6 Regulates Aggresome Formation and Cell Viability in Response to Misfolded Protein Stress , 2003, Cell.
[44] Ivan Dikic,et al. Nix is a selective autophagy receptor for mitochondrial clearance , 2010, EMBO reports.
[45] Sunhong Kim,et al. Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin , 2006, Nature.
[46] A. Whitworth,et al. Drosophila Parkin requires PINK1 for mitochondrial translocation and ubiquitinates Mitofusin , 2010, Proceedings of the National Academy of Sciences.
[47] S. Ralston,et al. Ubiquitin Recognition by the Ubiquitin-associated Domain of p62 Involves a Novel Conformational Switch* , 2008, Journal of Biological Chemistry.
[48] J. Opferman,et al. NIX is required for programmed mitochondrial clearance during reticulocyte maturation , 2007, Proceedings of the National Academy of Sciences.
[49] M. Riparbelli,et al. The Drosophila parkin homologue is required for normal mitochondrial dynamics during spermiogenesis. , 2007, Developmental biology.
[50] Robert W. Taylor,et al. High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease , 2006, Nature Genetics.
[51] R. Krüger,et al. Reduced Basal Autophagy and Impaired Mitochondrial Dynamics Due to Loss of Parkinson's Disease-Associated Protein DJ-1 , 2010, PloS one.
[52] D. Selkoe,et al. Pink1 Parkinson mutations, the Cdc37/Hsp90 chaperones and Parkin all influence the maturation or subcellular distribution of Pink1. , 2008, Human molecular genetics.
[53] D. Galter,et al. The MitoPark Mouse - an animal model of Parkinson's disease with impaired respiratory chain function in dopamine neurons. , 2009, Parkinsonism & related disorders.
[54] Y. Thielmann,et al. Nix directly binds to GABARAP: A possible crosstalk between apoptosis and autophagy , 2009, Autophagy.
[55] Li Chen,et al. α-Synuclein and Parkin Contribute to the Assembly of Ubiquitin Lysine 63-linked Multiubiquitin Chains* , 2005, Journal of Biological Chemistry.
[56] W. Craigen,et al. Neurologic Dysfunction and Male Infertility in Drosophila porin Mutants , 2010, The Journal of Biological Chemistry.
[57] D. Hernandez,et al. Lewy bodies and parkinsonism in families with parkin mutations , 2001, Annals of neurology.
[58] S. S. Mok,et al. Biochemical aspects of the neuroprotective mechanism of PTEN‐induced kinase‐1 (PINK1) , 2008, Journal of Neurochemistry.
[59] A. Haas,et al. A ubiquitin mutant with specific defects in DNA repair and multiubiquitination , 1995, Molecular and cellular biology.
[60] Hansong Deng,et al. The Parkinson's disease genes pink1 and parkin promote mitochondrial fission and/or inhibit fusion in Drosophila , 2008, Proceedings of the National Academy of Sciences.
[61] F. Sánchez‐Madrid,et al. HDAC6: a key regulator of cytoskeleton, cell migration and cell-cell interactions. , 2008, Trends in cell biology.
[62] S. Weber,et al. The PINK1/Parkin-mediated mitophagy is compromised by PD-associated mutations , 2010, Autophagy.
[63] M. Cookson,et al. The role of PTEN-induced kinase 1 in mitochondrial dysfunction and dynamics. , 2009, The international journal of biochemistry & cell biology.
[64] C. Ross,et al. Parkin Mediates Nonclassical, Proteasomal-Independent Ubiquitination of Synphilin-1: Implications for Lewy Body Formation , 2005, The Journal of Neuroscience.
[65] V. Shoshan-Barmatz,et al. Misfolded Mutant SOD1 Directly Inhibits VDAC1 Conductance in a Mouse Model of Inherited ALS , 2010, Neuron.
[66] V. De Pinto,et al. VDAC, a multi-functional mitochondrial protein regulating cell life and death. , 2010, Molecular aspects of medicine.
[67] James Lowe,et al. Depletion of 26S Proteasomes in Mouse Brain Neurons Causes Neurodegeneration and Lewy-Like Inclusions Resembling Human Pale Bodies , 2008, The Journal of Neuroscience.
[68] Hitoshi Takahashi,et al. The Lewy body in Parkinson's disease: Molecules implicated in the formation and degradation of α‐synuclein aggregates , 2007, Neuropathology : official journal of the Japanese Society of Neuropathology.
[69] K. Xia,et al. Association of PINK1 and DJ-1 confers digenic inheritance of early-onset Parkinson's disease. , 2006, Human molecular genetics.
[70] Steven P Gygi,et al. A proteomics approach to understanding protein ubiquitination , 2003, Nature Biotechnology.
[71] C. Geula,et al. Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons , 2006, Nature Genetics.
[72] A. Pestronk,et al. Familial parkinsonism and ophthalmoplegia from a mutation in the mitochondrial DNA helicase twinkle. , 2007, Archives of neurology.
[73] N. Hattori,et al. Diverse Effects of Pathogenic Mutations of Parkin That Catalyze Multiple Monoubiquitylation in Vitro* , 2006, Journal of Biological Chemistry.
[74] Changan Jiang,et al. Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin , 2006, Nature.
[75] T. Kerppola,et al. Lysosomal localization of ubiquitinated Jun requires multiple determinants in a lysine-27-linked polyubiquitin conjugate. , 2008, Molecular biology of the cell.
[76] C. Masters,et al. C-terminal truncation and Parkinson's disease-associated mutations down-regulate the protein serine/threonine kinase activity of PTEN-induced kinase-1. , 2006, Human molecular genetics.
[77] Nobutaka Hattori,et al. Association of DJ-1 and parkin mediated by pathogenic DJ-1 mutations and oxidative stress. , 2005, Human molecular genetics.
[78] Ivan Dikic,et al. A role for ubiquitin in selective autophagy. , 2009, Molecular cell.
[79] S. Biskup,et al. Detrimental deletions: mitochondria, aging and Parkinson's disease. , 2006, BioEssays : news and reviews in molecular, cellular and developmental biology.
[80] J. Taylor,et al. HDAC6 controls autophagosome maturation essential for ubiquitin‐selective quality‐control autophagy , 2010, The EMBO journal.
[81] Leonidas Stefanis,et al. Impaired degradation of mutant alpha-synuclein by chaperone-mediated autophagy. , 2004, Science.
[82] 佐藤 栄人. 14-3-3η is a novel regulator of parkin ubiquitin-ligase , 2004 .
[83] Michael R. Duchen,et al. PINK1-Associated Parkinson's Disease Is Caused by Neuronal Vulnerability to Calcium-Induced Cell Death , 2009, Molecular cell.
[84] R. Nussbaum,et al. Parkinson Phenotype in Aged PINK1-Deficient Mice Is Accompanied by Progressive Mitochondrial Dysfunction in Absence of Neurodegeneration , 2009, PloS one.
[85] John Rush,et al. Quantitative Proteomics Reveals the Function of Unconventional Ubiquitin Chains in Proteasomal Degradation , 2009, Cell.
[86] N. Wood,et al. Expanding insights of mitochondrial dysfunction in Parkinson's disease , 2006, Nature Reviews Neuroscience.
[87] J. C. Greene,et al. Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[88] Keiji Tanaka,et al. Does impairment of the ubiquitin-proteasome system or the autophagy-lysosome pathway predispose individuals to neurodegenerative disorders such as Parkinson's disease? , 2010, Journal of Alzheimer's disease : JAD.
[89] K. Lohmann,et al. Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patients. , 2010, Human molecular genetics.
[90] K. Lim,et al. Relative Sensitivity of Parkin and Other Cysteine-containing Enzymes to Stress-induced Solubility Alterations* , 2007, Journal of Biological Chemistry.
[91] E. Schon,et al. The kinase domain of mitochondrial PINK1 faces the cytoplasm , 2008, Proceedings of the National Academy of Sciences.
[92] O. Shirihai,et al. What can mitochondrial heterogeneity tell us about mitochondrial dynamics and autophagy? , 2009, The international journal of biochemistry & cell biology.
[93] N. Hattori,et al. Parkin binds the Rpn10 subunit of 26S proteasomes through its ubiquitin‐like domain , 2003, EMBO reports.
[94] R. J. Kelleher,et al. Loss of leucine-rich repeat kinase 2 causes impairment of protein degradation pathways, accumulation of α-synuclein, and apoptotic cell death in aged mice , 2010, Proceedings of the National Academy of Sciences.
[95] N. Hattori,et al. PINK1 is recruited to mitochondria with parkin and associates with LC3 in mitophagy , 2010, FEBS letters.
[96] Min Wu,et al. Fission and selective fusion govern mitochondrial segregation and elimination by autophagy , 2008, The EMBO journal.
[97] T. Dawson,et al. Response to Comment on "S-Nitrosylation of Parkin Regulates Ubiquitination and Compromises Parkin's Protective Function" , 2005, Science.
[98] Steve D. M. Brown,et al. α-Synuclein impairs macroautophagy: implications for Parkinson’s disease , 2010, The Journal of cell biology.
[99] C. Chu,et al. Role of autophagy in G2019S‐LRRK2‐associated neurite shortening in differentiated SH‐SY5Y cells , 2008, Journal of neurochemistry.
[100] R. Youle,et al. Parkin overexpression selects against a deleterious mtDNA mutation in heteroplasmic cybrid cells , 2010, Proceedings of the National Academy of Sciences.
[101] Armin Giese,et al. Inhibition of mitochondrial fusion by α‐synuclein is rescued by PINK1, Parkin and DJ‐1 , 2010, The EMBO journal.
[102] R. Kopito,et al. HDAC6 and Microtubules Are Required for Autophagic Degradation of Aggregated Huntingtin* , 2005, Journal of Biological Chemistry.
[103] M. Russo,et al. The Parkinson-associated protein PINK1 interacts with Beclin1 and promotes autophagy , 2010, Cell Death and Differentiation.
[104] David S. Park,et al. Loss of the Parkinson's disease-linked gene DJ-1 perturbs mitochondrial dynamics. , 2010, Human molecular genetics.
[105] YongSung Kim,et al. PINK1 controls mitochondrial localization of Parkin through direct phosphorylation. , 2008, Biochemical and biophysical research communications.
[106] R. Palmiter,et al. Parkin-mediated K63-linked polyubiquitination targets misfolded DJ-1 to aggresomes via binding to HDAC6 , 2007, The Journal of cell biology.
[107] P. Tienari,et al. Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease , 2007, Neurology.
[108] Nobutaka Hattori,et al. p62/SQSTM1 cooperates with Parkin for perinuclear clustering of depolarized mitochondria , 2010, Genes to cells : devoted to molecular & cellular mechanisms.
[109] R. Youle,et al. Parkin is recruited selectively to impaired mitochondria and promotes their autophagy , 2008, The Journal of cell biology.
[110] J. Schulz,et al. Therapeutic strategies for Parkinson's disease based on data derived from genetic research , 2003, Journal of Neurology.
[111] M. LaVoie,et al. The effects of oxidative stress on parkin and other E3 ligases , 2007, Journal of neurochemistry.
[112] E. Valente,et al. Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism. , 2005, Human molecular genetics.
[113] Wolfgang Wurst,et al. Loss of Parkin or PINK1 Function Increases Drp1-dependent Mitochondrial Fragmentation* , 2009, The Journal of Biological Chemistry.
[114] M. Nielsen,et al. Caspase-mediated Parkin Cleavage in Apoptotic Cell Death* , 2002, The Journal of Biological Chemistry.
[115] N. Avadhani,et al. Mitochondrial Import and Accumulation of α-Synuclein Impair Complex I in Human Dopaminergic Neuronal Cultures and Parkinson Disease Brain* , 2008, Journal of Biological Chemistry.
[116] Ted M. Dawson,et al. PINK1-dependent recruitment of Parkin to mitochondria in mitophagy , 2009, Proceedings of the National Academy of Sciences.
[117] A. Brice,et al. A regulated interaction with the UIM protein Eps15 implicates parkin in EGF receptor trafficking and PI(3)K–Akt signalling , 2006, Nature Cell Biology.
[118] L. Chin,et al. Phosphorylation of parkin by Parkinson disease-linked kinase PINK1 activates parkin E3 ligase function and NF-kappaB signaling. , 2010, Human molecular genetics.
[119] G. Dorn,et al. Nix Is Critical to Two Distinct Phases of Mitophagy, Reactive Oxygen Species-mediated Autophagy Induction and Parkin-Ubiquitin-p62-mediated Mitochondrial Priming* , 2010, The Journal of Biological Chemistry.
[120] W. Dauer,et al. Parkinson's Disease Mechanisms and Models , 2003, Neuron.
[121] D. Selkoe,et al. Dopamine covalently modifies and functionally inactivates parkin , 2005, Nature Medicine.
[122] Shinsei Minoshima,et al. Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase , 2000, Nature Genetics.
[123] V. Rybin,et al. HDAC6–p97/VCP controlled polyubiquitin chain turnover , 2006, The EMBO journal.
[124] D. Moore. Parkin: a multifaceted ubiquitin ligase. , 2006, Biochemical Society transactions.
[125] K. Dev,et al. The Cellular Protein Level of Parkin Is Regulated by Its Ubiquitin-like Domain* , 2003, The Journal of Biological Chemistry.
[126] Dan Garza,et al. HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPS , 2007, Nature.
[127] Joachim Klose,et al. Mitochondrial Dysfunction and Oxidative Damage in parkin-deficient Mice* , 2004, Journal of Biological Chemistry.
[128] Richard Wade-Martins,et al. LRRK2 regulates autophagic activity and localizes to specific membrane microdomains in a novel human genomic reporter cellular model. , 2009, Human molecular genetics.
[129] Angela C. Poole,et al. The Mitochondrial Fusion-Promoting Factor Mitofusin Is a Substrate of the PINK1/Parkin Pathway , 2010, PloS one.
[130] Ruifeng Lu,et al. Drosophila Overexpressing Parkin R275W Mutant Exhibits Dopaminergic Neuron Degeneration and Mitochondrial Abnormalities , 2007, The Journal of Neuroscience.
[131] N. Krishna,et al. Sequestosome 1/p62 Is a Polyubiquitin Chain Binding Protein Involved in Ubiquitin Proteasome Degradation , 2004, Molecular and Cellular Biology.
[132] T. Dawson,et al. Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[133] N. Hattori,et al. Parkin stabilizes PINK1 through direct interaction. , 2009, Biochemical and biophysical research communications.
[134] N. Hattori,et al. An Unfolded Putative Transmembrane Polypeptide, which Can Lead to Endoplasmic Reticulum Stress, Is a Substrate of Parkin , 2001, Cell.
[135] Jennifer Lippincott-Schwartz,et al. Ubiquitin signals autophagic degradation of cytosolic proteins and peroxisomes , 2008, Proceedings of the National Academy of Sciences.
[136] Atsushi Tanaka,et al. PINK1 Is Selectively Stabilized on Impaired Mitochondria to Activate Parkin , 2010, PLoS biology.
[137] C. Shults. Lewy bodies. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[138] S. Tabrizi,et al. Correction: PINK1 Is Necessary for Long Term Survival and Mitochondrial Function in Human Dopaminergic Neurons , 2008, PLoS ONE.
[139] P. Lackner,et al. Pathogenic mutations inactivate parkin by distinct mechanisms , 2005, Journal of neurochemistry.
[140] Isidre Ferrer,et al. Altered mitochondria, energy metabolism, voltage-dependent anion channel, and lipid rafts converge to exhaust neurons in Alzheimer’s disease , 2009, Journal of bioenergetics and biomembranes.
[141] Tobias M. Rasse,et al. Knockdown of transactive response DNA‐binding protein (TDP‐43) downregulates histone deacetylase 6 , 2010, The EMBO journal.
[142] P. Verstreken,et al. Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function , 2009, EMBO molecular medicine.
[143] P. Frachon,et al. Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins. , 2002, Molecular biology of the cell.
[144] M. Cookson,et al. Pink1 forms a multiprotein complex with Miro and Milton, linking Pink1 function to mitochondrial trafficking. , 2009, Biochemistry.
[145] G. Mardon,et al. Drosophila parkin mutants have decreased mass and cell size and increased sensitivity to oxygen radical stress , 2004, Development.
[146] N. Wood,et al. Mitochondrial function and morphology are impaired in parkin‐mutant fibroblasts , 2008, Annals of neurology.