The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
A Complete Genetic Analysis of Neuronal Rab3 Function
Open accessAbstract
Rab3A, Rab3B, Rab3C, and Rab3D are closely related GTP-binding proteins of synaptic vesicles that may function in neurotransmitter release. We have produced knock-out (KO) mice for Rab3B and Rab3C and crossed them with previously generated Rab3A and 3D knock-out mice to generate double, triple, and quadruple Rab3 knock-out mice. We have found that all single and double Rab3 knock-out mice are viable and fertile. Most triple Rab3 knock-out mice perish whenever Rab3A is one of the three deleted proteins, whereas all triple knock-out mice that express Rab3A are viable and fertile. Finally, all quadruple knock-out mice die shortly after birth. Quadruple Rab3 KO mice initially develop normally and are born alive but succumb to respiratory failure. Rab3-deficient mice display no apparent changes in synapse structure or brain composition except for a loss of rabphilin, a Rab3-binding protein. Analysis of cultured hippocampal neurons from quadruple knock-out mice uncovered no significant change in spontaneous or sucrose-evoked release but an ∼30% decrease in evoked responses. This decrease was caused by a decline in the synaptic and the vesicular release probabilities, suggesting that Rab3 proteins are essential for the normal regulation of Ca 2+ -triggered synaptic vesicle exocytosis but not for synaptic vesicle exocytosis as such. Our data show that Rab3 is required for survival in mice and that the four Rab3 proteins are functionally redundant in this role. Furthermore, our data demonstrate that Rab3 is not in itself essential for synaptic membrane traffic but functions to modulate the basic release machinery.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Essential functions of synapsins I and II in synaptic vesicle regulation
Rosahl, T. W., Spillane, D., Missler, M., Herz, J., Selig, D. K., Wolff, J. R., Hammer, R. E., Malenka, R. C., & Südhof, T. C. (1995) · Nature · doi:10.1038/375488a0 · Cited by 719
Self-citationRIM1α forms a protein scaffold for regulating neurotransmitter release at the active zone
Schoch, S., Castillo, P. E., Jo, T., Mukherjee, K., Geppert, M., Wang, Y., Schmitz, F., Malenka, R. C., & Südhof, T. C. (2002) · Nature · doi:10.1038/415321a · Cited by 579
Self-citation
Cited by
RIM determines Ca2+ channel density and vesicle docking at the presynaptic active zone
Han, Y., Kaeser, P. S., Südhof, T. C., & Schneggenburger, R. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.014 · Cited by 354
Self-citationSynaptic vesicle recycling: steps and principles
Rizzoli, S. O. (2014) · The EMBO Journal · doi:10.1002/embj.201386357 · Cited by 317
A Munc13/RIM/Rab3 tripartite complex: from priming to plasticity?
Dulubova, I., Lou, X., Lu, J., Huryeva, I., Alam, A., Schneggenburger, R., Südhof, T. C., & Rizo, J. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600753 · Cited by 289
Self-citationMunc13 C2B domain is an activity-dependent Ca2+ regulator of synaptic exocytosis
Shin, O.-H., Lu, J., Rhee, J.-S., Tomchick, D. R., Pang, Z. P., Wojcik, S. M., Camacho-Perez, M., Brose, N., Machius, M., Rizo, J., et al. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1758 · Cited by 243
Self-citationRab3 superprimes synaptic vesicles for release: implications for short-term synaptic plasticity
Schlüter, O. M., Basu, J., Südhof, T. C., & Rosenmund, C. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3553-05.2006 · Cited by 199
“We see an initial reduction in the EPSC amplitude but no change in vesicle pool size in Rab3-deficient neurons (Schluter et al., 2004).”
BackgroundMethodResultInfluentialSelf-citationUdayar, V., Buggia-Prévot, V., Guerreiro, R. L., Siegel, G., Rambabu, N., Soohoo, A. L., Ponnusamy, M., Siegenthaler, B., Bali, J., Guerreiro, R., et al. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.12.005 · Cited by 147
Deery, M. J., Maywood, E. S., Chesham, J. E., Sládek, M., Karp, N. A., Green, E. W., Charles, P. D., Reddy, A. B., Kyriacou, C. P., Lilley, K. S., et al. (2009) · Current Biology · doi:10.1016/j.cub.2009.10.024 · Cited by 125
Rab10 is involved in basolateral transport in polarized Madin-Darby canine kidney cells
Schuck, S., Gerl, M. J., Ang, A., Manninen, A., Keller, P., Mellman, I., & Simons, K. (2007) · Traffic · doi:10.1111/j.1600-0854.2006.00506.x · Cited by 117
Molecular Mechanisms Underlying Synaptic and Axon Degeneration in Parkinson’s Disease
Gcwensa, N. Z., Russell, D. L., Cowell, R. M., & Volpicelli-Daley, L. A. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.626128 · Cited by 110
Heterodimerization of Munc13 C2A domain with RIM regulates synaptic vesicle docking and priming
Camacho, M., Basu, J., Trimbuch, T., Chang, S., Pulido-Lozano, C., Chang, S.-S., Duluvova, I., Abo-Rady, M., Rizo, J., & Rosenmund, C. (2017) · Nature Communications · doi:10.1038/ncomms15293 · Cited by 95
Self-citationDe Pace, R., Britt, D. J., Mercurio, J., Foster, A. M., Djavaherian, L., Hoffmann, V., Abebe, D., & Bonifacino, J. S. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107775 · Cited by 87
Tsetsenis, T., Younts, T. J., Chiu, C. Q., Kaeser, P. S., Castillo, P. E., & Südhof, T. C. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1112237108 · Cited by 81
Self-citationRab GTPases implicated in inherited and acquired disorders
Mitra, S., Cheng, K. W., & Mills, G. B. (2011) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2010.12.005 · Cited by 78
ETS-4 Is a Transcriptional Regulator of Life Span in Caenorhabditis elegans
Thyagarajan, B., Blaszczak, A. G., Chandler, K. J., Watts, J. L., Johnson, W. E., & Graves, B. J. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001125 · Cited by 51
JIP1 Mediates Anterograde Transport of Rab10 Cargos during Neuronal Polarization
Deng, C.-Y., Lei, W.-L., Xu, X.-H., Ju, X.-C., Liu, Y., & Luo, Z.-G. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4496-13.2014 · Cited by 60
Sekine, Y., Lin-Moore, A., Chenette, D. M., Wang, X., Jiang, Z., Cafferty, W. B., Hammarlund, M., & Strittmatter, S. M. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.03.058 · Cited by 52
Presynaptic active zone density during development and synaptic plasticity
Clarke, G. L. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00012 · Cited by 33
Role of Rab27 in synaptic transmission at the squid giant synapse
Yu, E., Kanno, E., Choi, S., Sugimori, M., Moreira, J. E., Llinás, R. R., & Fukuda, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804825105 · Cited by 31
Molecular Mechanism of Active Zone Organization at Vertebrate Neuromuscular Junctions
Nishimune, H. (2012) · Molecular Neurobiology · doi:10.1007/s12035-011-8216-y · Cited by 29
“suggesting that the intracellular signaling for active zone organization is different between Drosophila and mice [174].”
BackgroundRAB3 phosphorylation by pathogenic LRRK2 impairs trafficking of synaptic vesicle precursors
Dou, D., Aiken, J., & Holzbaur, E. L. F. (2024) · Journal of Cell Biology · doi:10.1083/jcb.202307092 · Cited by 29
Mono-ubiquitination of Rabphilin 3A by UBE3A serves a non-degradative function
Avagliano Trezza, R., Punt, A. M., Mientjes, E., van den Berg, M., Zampeta, F. I., de Graaf, I. J., van der Weegen, Y., Demmers, J. A. A., Elgersma, Y., & Distel, B. (2021) · Scientific Reports · doi:10.1038/s41598-021-82319-9 · Cited by 16
RIM and MUNC13 membrane–binding domains are essential for neuropeptide secretion
Murphy, F. H., Abramian, A., Klaassen, R. V., Koopmans, F., Persoon, C. M., Smit, A. B., Toonen, R. F., & Verhage, M. (2025) · Journal of Cell Biology · doi:10.1083/jcb.202409196 · Cited by 3
Metadata
- Authors
- Schlüter, O. M., Schmitz, F., Jahn, R., Rosenmund, C., & Südhof, T. C.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2004-07-21
- Volume
- 24
- Issue
- 29
- Pages
- 6629-6637
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- OpenAlex
- W2164646446
- Cited by
- 302
- References
- 2
- FWCI
- 5.58
- Type
- journal article
- Language
- en
- Open access
- hybrid
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.