The DOI matches its Crossref record; 62 of the 62 references it cites were found in a registry or an index.
Rab7 Associates with Early Endosomes to Mediate Sorting and Transport of Semliki Forest Virus to Late Endosomes
Open accessAbstract
Semliki forest virus (SFV) is internalized by clathrin-mediated endocytosis, and transported via early endosomes to late endosomes and lysosomes. The intracellular pathway taken by individual fluorescently labeled SFV particles was followed using immunofluorescence in untransfected cells, and by video-enhanced, triple-color fluorescence microscopy in live cells transfected with GFP- and RFP-tagged Rab5, Rab7, Rab4, and Arf1. The viruses progressed from Rab5-positive early endosomes to a population of early endosomes (about 10% of total) that contained both Rab5 and Rab7. SFV were sequestered in the Rab7 domains, and they were sorted away from the early endosomes when these domains detached as separate transport carriers devoid of Rab5, Rab4, EEA1, Arf1, and transferrin. The process was independent of Arf1 and the acidic pH in early endosomes. Nocodazole treatment showed that the release of transport carriers was assisted by microtubules. Expression of constitutively inactive Rab7T22N resulted in accumulation of SFV in early endosomes. We concluded that Rab7 is recruited to early endosomes, where it forms distinct domains that mediate cargo sorting as well as the formation of late-endosome-targeted transport vesicles.
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
Rab proteins as membrane organizers
Zerial, M., & McBride, H. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35052055 · Cited by 3,381
A monomeric red fluorescent protein
Campbell, R. E., Tour, O., Palmer, A. E., Steinbach, P. A., Baird, G. S., Zacharias, D. A., & Tsien, R. Y. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.082243699 · Cited by 2,365
Ohkuma, S., & Poole, B. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.7.3327 · Cited by 2,174
Emergent Properties of Networks of Biological Signaling Pathways
Bhalla, U. S., & Iyengar, R. (1999) · Science · doi:10.1126/science.283.5400.381 · Cited by 1,686
Kornfeld, S., & Mellman, I. (1989) · Annual Review of Cell Biology · doi:10.1146/annurev.cb.05.110189.002411 · Cited by 1,580
The small GTPase rab5 functions as a regulatory factor in the early endocytic pathway
Bucci, C., Parton, R. G., Mather, I. H., Stunnenberg, H., Simons, K., Hoflack, B., & Zerial, M. (1992) · Cell · doi:10.1016/0092-8674(92)90306-w · Cited by 1,373
Localization of low molecular weight GTP binding proteins to exocytic and endocytic compartments
Chavrier, P., Parton, R. G., Hauri, H. P., Simons, K., & Zerial, M. (1990) · Cell · doi:10.1016/0092-8674(90)90369-p · Cited by 1,166
EEA1 links PI(3)K function to Rab5 regulation of endosome fusion
Simonsen, A., Lippe, R., Christoforidis, S., Gaullier, J.-M., Brech, A., Callaghan, J., Toh, B.-H., Murphy, C., Zerial, M., & Stenmark, H. (1998) · Nature · doi:10.1038/28879 · Cited by 1,133
rab5 controls early endosome fusion in vitro
Gorvel, J.-P., Chavrier, P., Zerial, M., & Gruenberg, J. (1991) · Cell · doi:10.1016/0092-8674(91)90316-q · Cited by 1,093
Rab7: A Key to Lysosome Biogenesis
Bucci, C., Thomsen, P., Nicoziani, P., McCarthy, J., & van Deurs, B. (2000) · Molecular Biology of the Cell · doi:10.1091/mbc.11.2.467 · Cited by 1,085
Sönnichsen, B., De Renzis, S., Nielsen, E., Rietdorf, J., & Zerial, M. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.149.4.901 · Cited by 919
The Rab5 effector EEA1 is a core component of endosome docking
Christoforidis, S., McBride, H. M., Burgoyne, R. D., & Zerial, M. (1999) · Nature · doi:10.1038/17618 · Cited by 854
On the entry of semliki forest virus into BHK-21 cells
Helenius, A., Kartenbeck, J., Simons, K., & Fries, E. (1980) · The Journal of Cell Biology · doi:10.1083/jcb.84.2.404 · Cited by 807
Self-citationThe diversity of Rab proteins in vesicle transport
Novick, P., & Zerial, M. (1997) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(97)80025-7 · Cited by 757
The biogenesis of multivesicular endosomes
Gruenberg, J., & Stenmark, H. (2004) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1360 · Cited by 723
The endocytic pathway: a mosaic of domains
Gruenberg, J. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35096054 · Cited by 702
The small GTP-binding protein rab4 controls an early sorting event on the endocytic pathway
van der Sluijs, P., Hull, M., Webster, P., Mâle, P., Goud, B., & Mellman, I. (1992) · Cell · doi:10.1016/0092-8674(92)90307-x · Cited by 685
Hrs sorts ubiquitinated proteins into clathrin-coated microdomains of early endosomes
Raiborg, C., Bache, K. G., Gillooly, D. J., Madshus, I. H., Stang, E., & Stenmark, H. (2002) · Nature Cell Biology · doi:10.1038/ncb791 · Cited by 652
Rab 7: an important regulator of late endocytic membrane traffic.
Feng, Y., Press, B., & Wandinger-Ness, A. (1995) · The Journal of cell biology · doi:10.1083/jcb.131.6.1435 · Cited by 638
Marsh, M., & Helenius, A. (1989) · Advances in Virus Research · doi:10.1016/s0065-3527(08)60583-7 · Cited by 602
Self-citationNot just a sink: endosomes in control of signal transduction
Miaczynska, M., Pelkmans, L., & Zerial, M. (2004) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2004.06.005 · Cited by 539
Pelkmans, L., Bürli, T., Zerial, M., & Helenius, A. (2004) · Cell · doi:10.1016/j.cell.2004.09.003 · Cited by 536
Self-citationRab GTPases: specifying and deciphering organelle identity and function
Pfeffer, S. R. (2001) · Trends in Cell Biology · doi:10.1016/s0962-8924(01)02147-x · Cited by 527
Rab5 regulates motility of early endosomes on microtubules
Nielsen, E., Severin, F., Backer, J. M., Hyman, A. A., & Zerial, M. (1999) · Nature Cell Biology · doi:10.1038/14075 · Cited by 510
Translocation and clustering of endosomes and lysosomes depends on microtubules.
Matteoni, R., & Kreis, T. E. (1987) · The Journal of cell biology · doi:10.1083/jcb.105.3.1253 · Cited by 494
Dissecting virus entry via endocytosis
Sieczkarski, S. B., & Whittaker, G. R. (2002) · Journal of General Virology · doi:10.1099/0022-1317-83-7-1535 · Cited by 487
Helenius, A., Mellman, I., Wall, D., & Hubbard, A. (1983) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(83)90350-x · Cited by 428
Self-citationVacuolar ATPase activity is required for endosomal carrier vesicle formation.
Clague, M. J., Urbé, S., Aniento, F., & Gruenberg, J. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)42302-7 · Cited by 416
Aniento, F. (1993) · The Journal of Cell Biology · doi:10.1083/jcb.123.6.1373 · Cited by 407
Sheff, D. R., Daro, E. A., Hull, M., & Mellman, I. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.145.1.123 · Cited by 399
Penetration of semliki forest virus from acidic prelysosomal vacuoles
Marsh, M., Bolzau, E., & Helenius, A. (1983) · Cell · doi:10.1016/0092-8674(83)90078-8 · Cited by 397
Self-citationKlimstra, W. B., Ryman, K. D., & Johnston, R. E. (1998) · Journal of Virology · doi:10.1128/jvi.72.9.7357-7366.1998 · Cited by 381
Adsorptive endocytosis of Semliki Forest virus
Marsh, M., & Helenius, A. (1980) · Journal of Molecular Biology · doi:10.1016/0022-2836(80)90281-8 · Cited by 348
Self-citationCarlsson, S. R., Roth, J., Piller, F., & Fukuda, M. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)37369-1 · Cited by 345
pH-dependent fusion between the Semliki Forest virus membrane and liposomes.
White, J., & Helenius, A. (1980) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.77.6.3273 · Cited by 344
Self-citationDivalent Rab effectors regulate the sub-compartmental organization and sorting of early endosomes
De Renzis, S., Sönnichsen, B., & Zerial, M. (2002) · Nature Cell Biology · doi:10.1038/ncb744 · Cited by 326
Bilayered Clathrin Coats on Endosomal Vacuoles Are Involved in Protein Sorting toward Lysosomes
Sachse, M., Urbé, S., Oorschot, V., Strous, G. J., & Klumperman, J. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.01-10-0525 · Cited by 321
Bomsel, M., Parton, R., Kuznetsov, S. A., Schroer, T. A., & Gruenberg, J. (1990) · Cell · doi:10.1016/0092-8674(90)90117-w · Cited by 299
The rab7 gtpase resides on a vesicular compartment connected to lysosomes
Méresse, S., Gorvel, J.-P., & Chavrier, P. (1995) · Journal of Cell Science · doi:10.1242/jcs.108.11.3349 · Cited by 296
Binding of Sindbis Virus to Cell Surface Heparan Sulfate
Byrnes, A. P., & Griffin, D. E. (1998) · Journal of Virology · doi:10.1128/jvi.72.9.7349-7356.1998 · Cited by 295
Cytoplasmic coat proteins involved in endosome function
Andrew Whitney, J., Gomez, M., Sheff, D., Kreis, T. E., & Mellman, I. (1995) · Cell · doi:10.1016/0092-8674(95)90183-3 · Cited by 284
The clathrin endocytic pathway in viral infection
DeTulleo, L. (1998) · The EMBO Journal · doi:10.1093/emboj/17.16.4585 · Cited by 281
Press, B., Feng, Y., Hoflack, B., & Wandinger-Ness, A. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.140.5.1075 · Cited by 267
Differential Requirements of Rab5 and Rab7 for Endocytosis of Influenza and Other Enveloped Viruses
Sieczkarski, S. B., & Whittaker, G. R. (2003) · Traffic · doi:10.1034/j.1600-0854.2003.00090.x · Cited by 223
Papini, E. (1997) · The EMBO Journal · doi:10.1093/emboj/16.1.15 · Cited by 217
Mancini, E. J., Clarke, M., Gowen, B. E., Rutten, T., & Fuller, S. D. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)80421-9 · Cited by 212
Membrane fusion of Semliki Forest virus involves homotrimers of the fusion protein
Wahlberg, J. M., Bron, R., Wilschut, J., & Garoff, H. (1992) · Journal of Virology · doi:10.1128/jvi.66.12.7309-7318.1992 · Cited by 210
Mosaic Organization of the Endocytic Pathway
Miaczynska, M., & Zerial, M. (2002) · Experimental Cell Research · doi:10.1006/excr.2001.5401 · Cited by 173
Herman, B. A., & Albertini, D. F. (1984) · The Journal of Cell Biology · doi:10.1083/jcb.98.2.565 · Cited by 157
Involvement of Ypt7p, a small GTPase, in traffic from late endosome to the vacuole in yeast
Schimmöller, F., & Riezman, H. (1993) · Journal of Cell Science · doi:10.1242/jcs.106.3.823 · Cited by 149
Inhibition of endocytosis by anti-clathrin antibodies
Doxsey, S., Brodsky, F. M., Blank, G. S., & Helenius, A. (1987) · Cell · doi:10.1016/0092-8674(87)90499-5 · Cited by 147
Self-citationMembrane fusion And the Alphavirus Life Cycle
Kielian, M. C. (1995) · Advances in virus research · doi:10.1016/s0065-3527(08)60059-7 · Cited by 144
Role of ribosomes in Semliki Forest virus nucleocapsid uncoating
Singh, I., & Helenius, A. (1992) · Journal of Virology · doi:10.1128/jvi.66.12.7049-7058.1992 · Cited by 140
Self-citationARF1 Regulates pH-dependent COP Functions in the Early Endocytic Pathway
Gu, F., & Grüenberg, J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.11.8154 · Cited by 137
Differential regulation of CXCR2 trafficking by Rab GTPases
Fan, G.-H., Lapierre, L. A., Goldenring, J. R., & Richmond, A. J. (2003) · Blood · doi:10.1182/blood-2002-07-1965 · Cited by 120
Dale, L. B., Seachrist, J. L., Babwah, A. V., & Ferguson, S. S. G. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313333200 · Cited by 116
Membrane fusion mutants of Semliki Forest virus.
Kielian, M. C., Keränen, S., Kääriäinen, L., & Helenius, A. (1984) · The Journal of Cell Biology · doi:10.1083/jcb.98.1.139 · Cited by 102
Self-citationMicrotubule and Motor-Dependent Endocytic Vesicle Sorting in Vitro
Bananis, E., Murray, J. W., Stockert, R. J., et al. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.1.179 · Cited by 93
Biogenesis of transport intermediates in the endocytic pathway
Gu, F., & Grüenberg, J. (1999) · FEBS Letters · doi:10.1016/s0014-5793(99)00561-x · Cited by 92
Smit, J. M., Waarts, B.-L., Kimata, K., Klimstra, W. B., Bittman, R., & Wilschut, J. (2002) · Journal of Virology · doi:10.1128/jvi.76.20.10128-10137.2002 · Cited by 88
Rab4 and Rab7 Define Distinct Nonoverlapping Endosomal Compartments
Bottger, G., Nagelkerken, B., & van der Sluijs, P. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.46.29191 · Cited by 83
Sequential Actions of Rab5 and Rab7 Regulate Endocytosis in the Xenopus Oocyte
Mukhopadhyay, A., Barbieri, A. M., Funato, K., Roberts, R., & Stahl, P. D. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.136.6.1227 · Cited by 68
Cited by
Mercer, J., Schelhaas, M., & Helenius, A. (2010) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060208-104626 · Cited by 1,057
Self-citationIdentification of the Switch in Early-to-Late Endosome Transition
Poteryaev, D., Datta, S., Ackema, K., Zerial, M., & Spang, A. (2010) · Cell · doi:10.1016/j.cell.2010.03.011 · Cited by 752
Rab Proteins and the Compartmentalization of the Endosomal System
Wandinger-Ness, A., & Zerial, M. (2014) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a022616 · Cited by 586
Lakadamyali, M., Rust, M. J., & Zhuang, X. (2006) · Cell · doi:10.1016/j.cell.2005.12.038 · Cited by 508
Dissecting the Cell Entry Pathway of Dengue Virus by Single-Particle Tracking in Living Cells
van der Schaar, H. M., Rust, M. J., Chen, C., van der Ende-Metselaar, H., Wilschut, J., Zhuang, X., & Smit, J. M. (2008) · PLoS Pathogens · doi:10.1371/journal.ppat.1000244 · Cited by 490
Metadata
- Authors
- Vonderheit, A., & Helenius, A.
- Venue
- PLoS Biology
- Publisher
- Public Library of Science (PLoS)
- Published
- 2005-06-21
- Volume
- 3
- Issue
- 7
- Pages
- e233
- ISSN
- 1544-9173 (ISSN-L)
- 1545-7885
- OpenAlex
- W2044191234
- Cited by
- 437
- References
- 62
- FWCI
- 6.55
- Type
- journal article
- Language
- en
- Open access
- gold
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.