Decoding Parkinson's Disease Pathogenesis: The Role of Deregulated mRNA Translation

scientific article published on 29 January 2016

Decoding Parkinson's Disease Pathogenesis: The Role of Deregulated mRNA Translation is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

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P356DOI10.3233/JPD-150738
P932PMC publication ID4927901
P698PubMed publication ID26889638

P2093author name stringIan Martin
P2860cites workGenetic perspective on the role of the autophagy-lysosome pathway in Parkinson diseaseQ22242985
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Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activityQ22254785
The Parkinson disease-linked LRRK2 protein mutation I2020T stabilizes an active state conformation leading to increased kinase activityQ24293505
Pathogenic LRRK2 negatively regulates microRNA-mediated translational repressionQ24293587
Leucine-rich repeat kinase 2 regulates autophagy through a calcium-dependent pathway involving NAADPQ24293723
Ribosomal protein s15 phosphorylation mediates LRRK2 neurodegeneration in Parkinson's diseaseQ24294458
Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomesQ24296835
Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALSQ24297462
The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activityQ24297634
LRRK2 controls an EndoA phosphorylation cycle in synaptic endocytosisQ24299176
LRRK2 kinase activity and biology are not uniformly predicted by its autophosphorylation and cellular phosphorylation site statusQ24300605
Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granulesQ24301077
Kinase activity of mutant LRRK2 mediates neuronal toxicityQ24303603
GTPase activity regulates kinase activity and cellular phenotypes of Parkinson's disease-associated LRRK2Q24306167
RNA binding activity of the recessive parkinsonism protein DJ-1 supports involvement in multiple cellular pathwaysQ24313263
RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson's disease riskQ24315688
Interplay of LRRK2 with chaperone-mediated autophagyQ24322747
Mutations in LRRK2 increase phosphorylation of peroxiredoxin 3 exacerbating oxidative stress-induced neuronal deathQ24323228
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson diseaseQ24336432
Loss of PINK1 attenuates HIF-1α induction by preventing 4E-BP1-dependent switch in protein translation under hypoxiaQ24337840
Parkinson's disease-associated mutations in LRRK2 link enhanced GTP-binding and kinase activities to neuronal toxicityQ24338647
Sustained translational repression by eIF2α-P mediates prion neurodegenerationQ24602153
Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALSQ24608159
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LRRK2 regulates autophagic activity and localizes to specific membrane microdomains in a novel human genomic reporter cellular modelQ24656256
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Cloning of the gene containing mutations that cause PARK8-linked Parkinson's diseaseQ28292932
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Editing-defective tRNA synthetase causes protein misfolding and neurodegenerationQ28590188
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LRRK2 phosphorylates moesin at threonine-558: characterization of how Parkinson's disease mutants affect kinase activityQ29615144
Kinase activity is required for the toxic effects of mutant LRRK2/dardarinQ29620478
Parthanatos mediates AIMP2-activated age-dependent dopaminergic neuronal lossQ30547326
The Parkinson's disease associated LRRK2 exhibits weaker in vitro phosphorylation of 4E-BP compared to autophosphorylationQ33525587
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Membrane recruitment of endogenous LRRK2 precedes its potent regulation of autophagyQ33920691
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The p38 subunit of the aminoacyl-tRNA synthetase complex is a Parkin substrate: linking protein biosynthesis and neurodegeneration.Q34202584
Phosphorylation of 4E-BP1 in the mammalian brain is not altered by LRRK2 expression or pathogenic mutationsQ34452296
Non-ATG-initiated translation directed by microsatellite expansionsQ34471662
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Profiling of Parkin-binding partners using tandem affinity purificationQ35045403
Autophosphorylation in the leucine-rich repeat kinase 2 (LRRK2) GTPase domain modifies kinase and GTP-binding activitiesQ35172817
LRRK2 protein levels are determined by kinase function and are crucial for kidney and lung homeostasis in miceQ35288337
Transcriptional responses to loss or gain of function of the leucine-rich repeat kinase 2 (LRRK2) gene uncover biological processes modulated by LRRK2 activityQ35605204
PINK1 and Parkin control localized translation of respiratory chain component mRNAs on mitochondria outer membrane.Q35684286
EIF4G1 mutations do not cause Parkinson's diseaseQ35732432
Roles of the Drosophila LRRK2 homolog in Rab7-dependent lysosomal positioningQ35771011
Impaired protein translation in Drosophila models for Charcot-Marie-Tooth neuropathy caused by mutant tRNA synthetasesQ35864966
G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodiesQ36143858
Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson diseaseQ36841500
Phosphorylation of 4E-BP by LRRK2 affects the maintenance of dopaminergic neurons in DrosophilaQ36891456
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Genetic animal models of Parkinson's diseaseQ37765030
LRRK2 pathobiology in Parkinson's diseaseQ38253871
Genetic ablation of ataxin-2 increases several global translation factors in their transcript abundance but decreases translation rateQ38300785
The PI3K/AKT Pathway as a Target for Cancer TreatmentQ38608907
DJ-1, a novel regulator of the tumor suppressor PTEN.Q39129969
Development of an enzyme-linked immunosorbent assay for detection of cellular and in vivo LRRK2 S935 phosphorylationQ41812724
Rapamycin activation of 4E-BP prevents parkinsonian dopaminergic neuron loss.Q41818673
CGG repeat-associated translation mediates neurodegeneration in fragile X tremor ataxia syndromeQ42068973
Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2.Q43280089
A continuous and direct assay to monitor leucine-rich repeat kinase 2 activityQ45814006
Differential effects of familial parkinson mutations in LRRK2 revealed by a systematic analysis of autophosphorylationQ47835833
Survey on the PABC recognition motif PAM2.Q47994563
Ser1292 autophosphorylation is an indicator of LRRK2 kinase activity and contributes to the cellular effects of PD mutationsQ48252778
EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohortsQ48256432
Investigation of leucine-rich repeat kinase 2 : enzymological properties and novel assays.Q54781213
Mechanistic insight into the dominant mode of the Parkinson's disease-associated G2019S LRRK2 mutationQ57373779
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Mutations in EIF4G1 are not a common cause of Parkinson's diseaseQ86380884
P275copyright licenseCreative Commons Attribution-NonCommercial 4.0 InternationalQ34179348
P433issue1
P407language of work or nameEnglishQ1860
P921main subjectParkinson's diseaseQ11085
messenger RNAQ188928
protein biosynthesisQ211935
pathogenesisQ372016
P5008on focus list of Wikimedia projectScienceSourceQ55439927
P304page(s)17-27
P577publication date2016-01-29
P1433published inJournal of Parkinson's diseaseQ26842319
P1476titleDecoding Parkinson's Disease Pathogenesis: The Role of Deregulated mRNA Translation
P478volume6

Reverse relations

cites work (P2860)
Q47331955Dynamic landscape of the local translation at activated synapses
Q99402075On the dynamical aspects of local translation at the activated synapse

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