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RAB7L1 Interacts with LRRK2 to Modify Intraneuronal Protein Sorting and Parkinson’s Disease Risk
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The endosomal network is a key biological pathway affected in neurodegenerative pathology.
“These studies, alongside clinical evidence [8][9][10][11][12][13][14], highlight the endosomal network as a key biological pathway affected in neurodegenerative pathology.”
From Global identification of neuronal and astrocytic integral membrane proteins that require Retromer for their endosomal recycling (2026) · cites this paper as [10]
Variants within the RAB29 and LRRK2 loci seem to impact Parkinson's disease in a non-additive manner, suggesting the two proteins function in a common cellular pathway.
“Variants within the RAB29 and the LRRK2 locus seem to impact PD in a non-additive manner [22,49,53], suggesting that the two proteins function in a common cellular pathway.”
From Distinct Roles for RAB10 and RAB29 in Pathogenic LRRK2-Mediated Endolysosomal Trafficking Alterations (2020) · cites this paper as [22]
Previous studies report a beneficial effect of increasing RAB29 protein levels on Golgi-lysosome sorting events, neurite outgrowth, and dopaminergic cell survival in Drosophila neurons.
“This finding is consistent with previous studies reporting a beneficial effect of increasing RAB29 protein levels on Golgi-lysosome sorting events, neurite outgrowth, and dopaminergic cell survival in Drosophila neurons, and with transcriptome analysis suggesting that RAB29 risk variants correlate with a decrease in RAB29 expression levels [22].”
From Distinct Roles for RAB10 and RAB29 in Pathogenic LRRK2-Mediated Endolysosomal Trafficking Alterations (2020) · cites this paper as [22]
Knockdown or knockout of RAB29 causes deficits in retrograde sorting events between the late endosome and the Golgi complex, which is crucial for the correct trafficking of lysosomal enzymes and associated with defects in lysosomal homeostasis.
“However, knockdown or knockout of RAB29 causes deficits in retrograde sorting events between the late endosome and the Golgi complex, which is crucial for the correct trafficking of lysosomal enzymes and associated with defects in lysosomal homeostasis [22,27,74].”
From Distinct Roles for RAB10 and RAB29 in Pathogenic LRRK2-Mediated Endolysosomal Trafficking Alterations (2020) · cites this paper as [22]
Transcriptome analysis suggests that RAB29 risk variants correlate with a decrease in RAB29 expression levels.
“and with transcriptome analysis suggesting that RAB29 risk variants correlate with a decrease in RAB29 expression levels [22].”
From Distinct Roles for RAB10 and RAB29 in Pathogenic LRRK2-Mediated Endolysosomal Trafficking Alterations (2020) · cites this paper as [22]
Pathogenic G2019S LRRK2 expression causes deficits in Golgi-lysosome-related sorting events, which are mimicked by knockdown of RAB29 and rescued by RAB29 overexpression, and decreased RAB29 levels correlate with increased Parkinson's disease risk.
“pathogenic G2019S LRRK2 expression causes deficits in Golgi-lysosome-related sorting events, which are mimicked by knockdown of RAB29 and rescued by RAB29 overexpression, respectively, and transcriptome and protein analyses indicate that decreased RAB29 levels correlate with increased PD risk [22].”
From Distinct Roles for RAB10 and RAB29 in Pathogenic LRRK2-Mediated Endolysosomal Trafficking Alterations (2020) · cites this paper as [22]
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Cites
Mice Lacking α-Synuclein Display Functional Deficits in the Nigrostriatal Dopamine System
Abeliovich, A., Schmitz, Y., Fariñas, I., Choi-Lundberg, D., Ho, W.-H., Castillo, P. E., Shinsky, N., Verdugo, J. M. G., Armanini, M., Ryan, A., et al. (2000) · Neuron · doi:10.1016/s0896-6273(00)80886-7 · Cited by 1,722
Self-citationTranscriptome genetics using second generation sequencing in a Caucasian population
Montgomery, S. B., Sammeth, M., Gutierrez-Arcelus, M., Lach, R. P., Ingle, C., Nisbett, J., Guigo, R., & Dermitzakis, E. T. (2010) · Nature · doi:10.1038/nature08903 · Cited by 797
Muhammad, A., Flores, I., Zhang, H., Yu, R., Staniszewski, A., Planel, E., Herman, M., Ho, L., Kreber, R., Honig, L. S., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802545105 · Cited by 248
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Research works printed but not linked: 45
- Abeliovich, 2006, Parkinsonism genes: culprits and clues, J. Neurochem., 99, 1062, 10.1111/j.1471-4159.2006.04102.x · DOI
- Andres-Mateos, 2009, Unexpected lack of hypersensitivity in LRRK2 knock-out mice to MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine), J. Neurosci., 29, 15846, 10.1523/JNEUROSCI.4357-09.2009 · DOI
- Arighi, 2004, Role of the mammalian retromer in sorting of the cation-independent mannose 6-phosphate receptor, J. Cell Biol., 165, 123, 10.1083/jcb.200312055 · DOI · Paper page
- Berger, 2009, Roles for endocytic trafficking and phosphatidylinositol 4-kinase III alpha in hepatitis C virus replication, Proc. Natl. Acad. Sci. USA, 106, 7577, 10.1073/pnas.0902693106 · DOI
- Biskup, 2006, Localization of LRRK2 to membranous and vesicular structures in mammalian brain, Ann. Neurol., 60, 557, 10.1002/ana.21019 · DOI
- Bonifacino, 2008, Retromer, Curr. Opin. Cell Biol., 20, 427, 10.1016/j.ceb.2008.03.009 · DOI · Paper page
- Cooper, 2006, Alpha-synuclein blocks ER-Golgi traffic and Rab1 rescues neuron loss in Parkinson’s models, Science, 313, 324, 10.1126/science.1129462 · DOI
- Dietzl, 2007, A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila, Nature, 448, 151, 10.1038/nature05954 · DOI · Paper page
- Dodson, 2012, Roles of the Drosophila LRRK2 homolog in Rab7-dependent lysosomal positioning, Hum. Mol. Genet., 21, 1350, 10.1093/hmg/ddr573 · DOI
- Feany, 2000, A Drosophila model of Parkinson’s disease, Nature, 404, 394, 10.1038/35006074 · DOI
- Fischer, 1988, GAL4 activates transcription in Drosophila, Nature, 332, 853, 10.1038/332853a0 · DOI
- Friggi-Grelin, 2003, Targeted gene expression in Drosophila dopaminergic cells using regulatory sequences from tyrosine hydroxylase, J. Neurobiol., 54, 618, 10.1002/neu.10185 · DOI
- Gan-Or, 2012, Association of sequence alterations in the putative promoter of RAB7L1 with a reduced Parkinson disease risk, Arch. Neurol., 69, 105, 10.1001/archneurol.2011.924 · DOI · Paper page
- Grill, 2007, C. elegans RPM-1 regulates axon termination and synaptogenesis through the Rab GEF GLO-4 and the Rab GTPase GLO-1, Neuron, 55, 587, 10.1016/j.neuron.2007.07.009 · DOI
- Hamza, 2010, Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson’s disease, Nat. Genet., 42, 781, 10.1038/ng.642 · DOI
- Hardy, 2006, Genetics of Parkinson’s disease and parkinsonism, Ann. Neurol., 60, 389, 10.1002/ana.21022 · DOI
- Heo, 2010, Coordinate regulation of neurite outgrowth by LRRK2 and its interactor, Rab5, Exp. Neurobiol., 19, 97, 10.5607/en.2010.19.2.97 · DOI
- Hermann, 2005, Genetic analysis of lysosomal trafficking in Caenorhabditis elegans, Mol. Biol. Cell, 16, 3273, 10.1091/mbc.e05-01-0060 · DOI
- Higashi, 2009, Abnormal localization of leucine-rich repeat kinase 2 to the endosomal-lysosomal compartment in Lewy body disease, J. Neuropathol. Exp. Neurol., 68, 994, 10.1097/NEN.0b013e3181b44ed8 · DOI
- Kim, 2010, Implication of mouse Vps26b-Vps29-Vps35 retromer complex in sortilin trafficking, Biochem. Biophys. Res. Commun., 403, 167, 10.1016/j.bbrc.2010.10.121 · DOI
- Lang, 1998, Parkinson’s disease. First of two parts, N. Engl. J. Med., 339, 1044, 10.1056/NEJM199810083391506 · DOI
- Latourelle, 2011, Genomewide linkage study of modifiers of LRRK2-related Parkinson’s disease, Mov. Disord., 26, 2039, 10.1002/mds.23781 · DOI
- Li, 2009, Mutant LRRK2(R1441G) BAC transgenic mice recapitulate cardinal features of Parkinson’s disease, Nat. Neurosci., 12, 826, 10.1038/nn.2349 · DOI
- Lill, 2012, Comprehensive research synopsis and systematic meta-analyses in Parkinson’s disease genetics: the PDGene database, PLoS Genet., 8, e1002548, 10.1371/journal.pgen.1002548 · DOI
- MacLeod, 2006, The familial Parkinsonism gene LRRK2 regulates neurite process morphology, Neuron, 52, 587, 10.1016/j.neuron.2006.10.008 · DOI
- Ng, 2009, Parkin protects against LRRK2 G2019S mutant-induced dopaminergic neurodegeneration in Drosophila, J. Neurosci., 29, 11257, 10.1523/JNEUROSCI.2375-09.2009 · DOI
- Piccoli, 2011, LRRK2 controls synaptic vesicle storage and mobilization within the recycling pool, J. Neurosci., 31, 2225, 10.1523/JNEUROSCI.3730-10.2011 · DOI
- Rhinn, 2008, Housekeeping while brain’s storming Validation of normalizing factors for gene expression studies in a murine model of traumatic brain injury, BMC Mol. Biol., 9, 62, 10.1186/1471-2199-9-62 · DOI
- Rogaeva, 2007, The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease, Nat. Genet., 39, 168, 10.1038/ng1943 · DOI · Paper page
- Rojas, 2008, Regulation of retromer recruitment to endosomes by sequential action of Rab5 and Rab7, J. Cell Biol., 183, 513, 10.1083/jcb.200804048 · DOI · Paper page
- Sakaguchi-Nakashima, 2007, LRK-1, a C. elegans PARK8-related kinase, regulates axonal-dendritic polarity of SV proteins, Curr Biol., 17, 592, 10.1016/j.cub.2007.01.074 · DOI
- Seaman, 2004, Cargo-selective endosomal sorting for retrieval to the Golgi requires retromer, J. Cell Biol., 165, 111, 10.1083/jcb.200312034 · DOI · Paper page
- Seaman, 1998, A membrane coat complex essential for endosome-to-Golgi retrograde transport in yeast, J. Cell Biol., 142, 665, 10.1083/jcb.142.3.665 · DOI · Paper page
- Shimizu, 1997, Cloning and chromosome assignment to 1q32 of a human cDNA (RAB7L1) encoding a small GTP-binding protein, a member of the RAS superfamily, Cytogenet. Cell Genet., 77, 261, 10.1159/000134591 · DOI
- Simón-Sánchez, 2009, Genome-wide association study reveals genetic risk underlying Parkinson’s disease, Nat. Genet., 41, 1308, 10.1038/ng.487 · DOI · Paper page
- Spanò, 2011, Proteolytic targeting of Rab29 by an effector protein distinguishes the intracellular compartments of human-adapted and broad-host Salmonella, Proc. Natl. Acad. Sci. USA, 108, 18418, 10.1073/pnas.1111959108 · DOI
- Stafa, 2012, GTPase activity and neuronal toxicity of Parkinson’s disease-associated LRRK2 is regulated by ArfGAP1, PLoS Genet., 8, e1002526, 10.1371/journal.pgen.1002526 · DOI · Paper page
- Thayanidhi, 2010, Alpha-synuclein delays endoplasmic reticulum (ER)-to-Golgi transport in mammalian cells by antagonizing ER/Golgi SNAREs, Mol. Biol. Cell, 21, 1850, 10.1091/mbc.e09-09-0801 · DOI
- Tong, 2009, R1441C mutation in LRRK2 impairs dopaminergic neurotransmission in mice, Proc. Natl. Acad. Sci. USA, 106, 14622, 10.1073/pnas.0906334106 · DOI
- Vilariño-Güell, 2011, VPS35 mutations in Parkinson disease, Am. J. Hum. Genet., 89, 162, 10.1016/j.ajhg.2011.06.001 · DOI · Paper page
- Wu, 2006, A protocol for dissecting Drosophila melanogaster brains for live imaging or immunostaining, Nat. Protoc., 1, 2110, 10.1038/nprot.2006.336 · DOI
- Xia, 1996, Calcium influx via the NMDA receptor induces immediate early gene transcription by a MAP kinase/ERK-dependent mechanism, J. Neurosci., 16, 5425, 10.1523/JNEUROSCI.16-17-05425.1996 · DOI
- Zhang, 2007, Thirty-one flavors of Drosophila Rab proteins, Genetics, 176, 1307, 10.1534/genetics.106.066761 · DOI
- Zheng, 2010, PGC-1α, a potential therapeutic target for early intervention in Parkinson’s disease, Sci. Transl. Med., 2, 52ra73, 10.1126/scitranslmed.3001059 · DOI
- Zimprich, 2011, A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease, Am. J. Hum. Genet., 89, 168, 10.1016/j.ajhg.2011.06.008 · DOI · Paper page
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Cullen, P. J., & Steinberg, F. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0053-7 · Cited by 590
Reduced glucocerebrosidase is associated with increased α-synuclein in sporadic Parkinson’s disease
Murphy, K. E., Gysbers, A. M., Abbott, S. K., Tayebi, N., Kim, W. S., Sidransky, E., Cooper, A., Garner, B., & Halliday, G. M. (2014) · Brain · doi:10.1093/brain/awt367 · Cited by 475
Zavodszky, E., Seaman, M. N. J., Moreau, K., Jimenez-Sanchez, M., Breusegem, S. Y., Harbour, M. E., & Rubinsztein, D. C. (2014) · Nature Communications · doi:10.1038/ncomms4828 · Cited by 466
Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance
Hernandez, D. G., Reed, X., & Singleton, A. B. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13593 · Cited by 448
Lucin, K. M., O’Brien, C. E., Bieri, G., Czirr, E., Mosher, K. I., Abbey, R. J., Mastroeni, D. F., Rogers, J., Spencer, B., Masliah, E., et al. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.046 · Cited by 374
Synaptopathies: synaptic dysfunction in neurological disorders – A review from students to students
Lepeta, K., Lourenco, M. V., Schweitzer, B. C., Martino Adami, P. V., Banerjee, P., Catuara‐Solarz, S., de La Fuente Revenga, M., Guillem, A. M., Haidar, M., Ijomone, O. M., et al. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13713 · Cited by 386
Tang, F.-L., Erion, J. R., Tian, Y., Liu, W., Yin, D.-M., Ye, J., Tang, B., Mei, L., & Xiong, W.-C. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0042-15.2015 · Cited by 269
Henry, A. G., Aghamohammadzadeh, S., Samaroo, H., Chen, Y., Mou, K., Needle, E., & Hirst, W. D. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddv314 · Cited by 235
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Ho, M. S. (2019) · Advances in Experimental Medicine and Biology · doi:10.1007/978-981-13-9913-8_13 · Cited by 227
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Zhang, Q., Pan, Y., Yan, R., Zeng, B., Wang, H., Zhang, X., Li, W., Wei, H., & Liu, Z. (2015) · Nature Immunology · doi:10.1038/ni.3233 · Cited by 206
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Gustavsson, E. K., Follett, J., Trinh, J., Barodia, S. K., Real, R., Liu, Z., Grant-Peters, M., Fox, J. D., Appel-Cresswell, S., Stoessl, A. J., et al. (2024) · The Lancet Neurology · doi:10.1016/s1474-4422(24)00121-2 · Cited by 114
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Kumaran, R., & Cookson, M. R. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddv236 · Cited by 86
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Rivero-Ríos, P., Romo-Lozano, M., Fernández, B., Fdez, E., & Hilfiker, S. (2020) · Cells · doi:10.3390/cells9071719 · Cited by 38
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Jones, E., Adams, H., Chen, K.-E., Maroof, F., Ibbotson, T. M., Nakamura, Y., Banks, P. J., Healy, M. D., Lewis, P. A., Heesom, K. J., et al. (2026) · doi:10.64898/2026.05.14.724903
Metadata
- Authors
- MacLeod, D. A., Rhinn, H., Kuwahara, T., Zolin, A., Di Paolo, G., McCabe, B. D., Marder, K. S., Honig, L. S., Clark, L. N., Small, S. A., & Abeliovich, A.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2013-02
- Volume
- 77
- Issue
- 3
- Pages
- 425-439
- ISSN
- 0896-6273
- PMC
- PMC3646583
- Cited by
- 516
- References
- 3
- Language
- en
- Update notices
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