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Journal articles on the topic 'CORVET'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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1

Hunter, Morag R., Edward J. Scourfield, Edward Emmott, and Stephen C. Graham. "VPS18 recruits VPS41 to the human HOPS complex via a RING–RING interaction." Biochemical Journal 474, no. 21 (2017): 3615–26. http://dx.doi.org/10.1042/bcj20170588.

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Eukaryotic cells use conserved multisubunit membrane tethering complexes, including CORVET (class C core vacuole/endosome tethering) and HOPS (homotypic fusion and vacuole protein sorting), to control the fusion of endomembranes. These complexes have been extensively studied in yeast, but to date there have been far fewer studies of metazoan CORVET and HOPS. Both of these complexes comprise six subunits: a common four-subunit core and two unique subunits. Once assembled, these complexes function to recognise specific endosomal membrane markers and facilitate SNARE-mediated membrane fusion. COR

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2

Markgraf, Daniel F., Franziska Ahnert, Henning Arlt, et al. "The CORVET Subunit Vps8 Cooperates with the Rab5 Homolog Vps21 to Induce Clustering of Late Endosomal Compartments." Molecular Biology of the Cell 20, no. 24 (2009): 5276–89. http://dx.doi.org/10.1091/mbc.e09-06-0521.

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Membrane tethering, the process of mediating the first contact between membranes destined for fusion, requires specialized multisubunit protein complexes and Rab GTPases. In the yeast endolysosomal system, the hexameric HOPS tethering complex cooperates with the Rab7 homolog Ypt7 to promote homotypic fusion at the vacuole, whereas the recently identified homologous CORVET complex acts at the level of late endosomes. Here, we have further functionally characterized the CORVET-specific subunit Vps8 and its relationship to the remaining subunits using an in vivo approach that allows the monitorin

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3

Takemoto, Kodai, Kazuo Ebine, Jana Christin Askani, et al. "Distinct sets of tethering complexes, SNARE complexes, and Rab GTPases mediate membrane fusion at the vacuole in Arabidopsis." Proceedings of the National Academy of Sciences 115, no. 10 (2018): E2457—E2466. http://dx.doi.org/10.1073/pnas.1717839115.

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Membrane trafficking plays pivotal roles in various cellular activities and higher-order functions of eukaryotes and requires tethering factors to mediate contact between transport intermediates and target membranes. Two evolutionarily conserved tethering complexes, homotypic fusion and protein sorting (HOPS) and class C core vacuole/endosome tethering (CORVET), are known to act in endosomal/vacuolar transport in yeast and animals. Both complexes share a core subcomplex consisting of Vps11, Vps18, Vps16, and Vps33, and in addition to this core, HOPS contains Vps39 and Vps41, whereas CORVET con

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4

Plemel, Rachael L., Braden T. Lobingier, Christopher L. Brett, et al. "Subunit organization and Rab interactions of Vps-C protein complexes that control endolysosomal membrane traffic." Molecular Biology of the Cell 22, no. 8 (2011): 1353–63. http://dx.doi.org/10.1091/mbc.e10-03-0260.

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Traffic through late endolysosomal compartments is regulated by sequential signaling of small G proteins of the Rab5 and Rab7 families. The Saccharomyces cerevisiae Vps-C protein complexes CORVET (class C core vacuole/endosome tethering complex) and HOPS (homotypic fusion and protein transport) interact with endolysosomal Rabs to coordinate their signaling activities. To better understand these large and intricate complexes, we performed interaction surveys to assemble domain-level interaction topologies for the eight Vps-C subunits. We identified numerous intersubunit interactions and up to s

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5

Solinger, Jachen A., and Anne Spang. "Tethering complexes in the endocytic pathway: CORVET and HOPS." FEBS Journal 280, no. 12 (2013): 2743–57. http://dx.doi.org/10.1111/febs.12151.

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6

Solinger, Jachen A., and Anne Spang. "Loss of the Sec1/Munc18-family proteins VPS-33.2 and VPS-33.1 bypasses a block in endosome maturation in Caenorhabditis elegans." Molecular Biology of the Cell 25, no. 24 (2014): 3909–25. http://dx.doi.org/10.1091/mbc.e13-12-0710.

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The end of the life of a transport vesicle requires a complex series of tethering, docking, and fusion events. Tethering complexes play a crucial role in the recognition of membrane entities and bringing them into close opposition, thereby coordinating and controlling cellular trafficking events. Here we provide a comprehensive RNA interference analysis of the CORVET and HOPS tethering complexes in metazoans. Knockdown of CORVET components promoted RAB-7 recruitment to subapical membranes, whereas in HOPS knockdowns, RAB-5 was found also on membrane structures close to the cell center, indicat

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7

Sparvoli, Daniela, Martin Zoltner, Chao-Yin Cheng, Mark C. Field, and Aaron P. Turkewitz. "Diversification of CORVET tethers facilitates transport complexity in Tetrahymena thermophila." Journal of Cell Science 133, no. 3 (2020): jcs238659. http://dx.doi.org/10.1242/jcs.238659.

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8

Chou, Hui-Ting, Danijela Dukovski, Melissa G. Chambers, Karin M. Reinisch, and Thomas Walz. "CATCHR, HOPS and CORVET tethering complexes share a similar architecture." Nature Structural & Molecular Biology 23, no. 8 (2016): 761–63. http://dx.doi.org/10.1038/nsmb.3264.

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9

Abenza, Juan F., Antonio Galindo, Areti Pantazopoulou, Concha Gil, Vivian de los Ríos, and Miguel A. Peñalva. "Aspergillus RabBRab5 Integrates Acquisition of Degradative Identity with the Long Distance Movement of Early Endosomes." Molecular Biology of the Cell 21, no. 15 (2010): 2756–69. http://dx.doi.org/10.1091/mbc.e10-02-0119.

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Aspergillus nidulans early endosomes display characteristic long-distance bidirectional motility. Simultaneous dual-channel acquisition showed that the two Rab5 paralogues RabB and RabA colocalize in these early endosomes and also in larger, immotile mature endosomes. However, RabB-GTP is the sole recruiter to endosomes of Vps34 PI3K (phosphatidylinositol-3-kinase) and the phosphatidylinositol-3-phosphate [PI(3)P] effector AnVps19 and rabBΔ, leading to thermosensitivity prevents multivesicular body sorting of endocytic cargo. Thus, RabB is the sole mediator of degradative endosomal identity. I

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10

Balderhaar, H. J. k., and C. Ungermann. "CORVET and HOPS tethering complexes - coordinators of endosome and lysosome fusion." Journal of Cell Science 126, no. 6 (2013): 1307–16. http://dx.doi.org/10.1242/jcs.107805.

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11

Balderhaar, H. J. k., J. Lachmann, E. Yavavli, C. Brocker, A. Lurick, and C. Ungermann. "The CORVET complex promotes tethering and fusion of Rab5/Vps21-positive membranes." Proceedings of the National Academy of Sciences 110, no. 10 (2013): 3823–28. http://dx.doi.org/10.1073/pnas.1221785110.

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12

Pavlova, Elena V., Aleksey Shatunov, Lena Wartosch, et al. "The lysosomal disease caused by mutant VPS33A." Human Molecular Genetics 28, no. 15 (2019): 2514–30. http://dx.doi.org/10.1093/hmg/ddz077.

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AbstractA rare lysosomal disease resembling a mucopolysaccharidosis with unusual systemic features, including renal disease and platelet dysfunction, caused by the defect in a conserved region of the VPS33A gene on human chromosome 12q24.31, occurs in Yakuts—a nomadic Turkic ethnic group of Southern Siberia. VPS33A is a core component of the class C core vacuole/endosome tethering (CORVET) and the homotypic fusion and protein sorting (HOPS) complexes, which have essential functions in the endocytic pathway. Here we show that cultured fibroblasts from patients with this disorder have morphologi

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13

Perini, Enrico D., Ramona Schaefer, Martin Stöter, Yannis Kalaidzidis, and Marino Zerial. "Mammalian CORVET Is Required for Fusion and Conversion of Distinct Early Endosome Subpopulations." Traffic 15, no. 12 (2014): 1366–89. http://dx.doi.org/10.1111/tra.12232.

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14

Guo, Zhong, Wayne Johnston, Oleksiy Kovtun, et al. "Subunit Organisation of In Vitro Reconstituted HOPS and CORVET Multisubunit Membrane Tethering Complexes." PLoS ONE 8, no. 12 (2013): e81534. http://dx.doi.org/10.1371/journal.pone.0081534.

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15

Aucoin, Martin, Georges Beaudoin, Robert A. Creaser, and Paul Archer. "Metallogeny of the Marco zone, Corvet Est, disseminated gold deposit, James Bay, Quebec, Canada." Canadian Journal of Earth Sciences 49, no. 10 (2012): 1154–76. http://dx.doi.org/10.1139/e2012-047.

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The Corvet Est gold deposit is hosted by Archean rocks of the Superior Province in the James Bay region, northern Quebec, Canada. The Marco zone is hosted by amphibolite-grade, strongly foliated volcanic rocks and consists of disseminated gold, with an apparent thickness ranging from 1.8 to 39.5 m and gold grades up to 23 g·t–1 over 1 m, that is continuous along strike for ∼1.3 km. The lithotectonic sequence comprises footwall basaltic andesite amphibolite overlain by a lenticular unit of metadacite and then by hanging-wall basaltic andesite amphibolite, all intruded by quartz–feldspar porphyr

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16

Numrich, Johannes, and Christian Ungermann. "Endocytic Rabs in membrane trafficking and signaling." Biological Chemistry 395, no. 3 (2014): 327–33. http://dx.doi.org/10.1515/hsz-2013-0258.

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Abstract The endolysosomal system controls the trafficking of proteins between the plasma membrane and the degradative environment of the lysosome. The early endosomal Rab5 and the late endosomal Rab7 GTPases have a key role in the transport along the endocytic pathway by recruiting tethering factors such as the hexameric CORVET and HOPS complexes that promote membrane fusion. Both Rabs are also involved in signaling at endosomal membranes and linked to amino acid sensing and autophagy, indicating that their role in trafficking may be connected to signal transduction and adaptation during cell

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17

van der Beek, Jan, Caspar Jonker, Reini van der Welle, Nalan Liv, and Judith Klumperman. "CORVET, CHEVI and HOPS – multisubunit tethers of the endo-lysosomal system in health and disease." Journal of Cell Science 132, no. 10 (2019): jcs189134. http://dx.doi.org/10.1242/jcs.189134.

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18

van der Kant, Rik, Caspar T. H. Jonker, Ruud H. Wijdeven, et al. "Characterization of the Mammalian CORVET and HOPS Complexes and Their Modular Restructuring for Endosome Specificity." Journal of Biological Chemistry 290, no. 51 (2015): 30280–90. http://dx.doi.org/10.1074/jbc.m115.688440.

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19

Morlon-Guyot, Juliette, Hiba El Hajj, Kevin Martin, et al. "A proteomic analysis unravels novel CORVET and HOPS proteins involved in Toxoplasma gondii secretory organelles biogenesis." Cellular Microbiology 20, no. 11 (2018): e12870. http://dx.doi.org/10.1111/cmi.12870.

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20

Lachmann, Jens, Elina Glaubke, Patrick S. Moore, and Christian Ungermann. "The Vps39-like TRAP1 is an effector of Rab5 and likely the missing Vps3 subunit of human CORVET." Cellular Logistics 4, no. 4 (2014): e970840. http://dx.doi.org/10.4161/21592780.2014.970840.

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21

Morlon-Guyot, Juliette, Sandra Pastore, Laurence Berry, Maryse Lebrun, and Wassim Daher. "Toxoplasma gondiiVps11, a subunit of HOPS and CORVET tethering complexes, is essential for the biogenesis of secretory organelles." Cellular Microbiology 17, no. 8 (2015): 1157–78. http://dx.doi.org/10.1111/cmi.12426.

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22

Peplowska, Karolina, Daniel F. Markgraf, Clemens W. Ostrowicz, Gert Bange, and Christian Ungermann. "The CORVET Tethering Complex Interacts with the Yeast Rab5 Homolog Vps21 and Is Involved in Endo-Lysosomal Biogenesis." Developmental Cell 12, no. 5 (2007): 739–50. http://dx.doi.org/10.1016/j.devcel.2007.03.006.

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23

Randhawa, Anmoldeep, Debasree Kundu, Anupam Sharma, Rajendra Prasad, and Alok K. Mondal. "Overexpression of the CORVET complex alleviates the fungicidal effects of fludioxonil on the yeastSaccharomyces cerevisiaeexpressing hybrid histidine kinase 3." Journal of Biological Chemistry 294, no. 2 (2018): 461–75. http://dx.doi.org/10.1074/jbc.ra118.004736.

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24

Marsalek, Lukas, Clemens Gruber, Friedrich Altmann, et al. "Disruption of genes involved in CORVET complex leads to enhanced secretion of heterologous carboxylesterase only in protease deficientPichia pastoris." Biotechnology Journal 12, no. 5 (2017): 1600584. http://dx.doi.org/10.1002/biot.201600584.

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25

Mackie, Timothy D., Bo-Young Kim, Arohan R. Subramanya, et al. "The endosomal trafficking factors CORVET and ESCRT suppress plasma membrane residence of the renal outer medullary potassium channel (ROMK)." Journal of Biological Chemistry 293, no. 9 (2018): 3201–17. http://dx.doi.org/10.1074/jbc.m117.819086.

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26

Cabrera, Margarita, Henning Arlt, Nadine Epp, et al. "Functional Separation of Endosomal Fusion Factors and the Class C Core Vacuole/Endosome Tethering (CORVET) Complex in Endosome Biogenesis." Journal of Biological Chemistry 288, no. 7 (2012): 5166–75. http://dx.doi.org/10.1074/jbc.m112.431536.

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27

Sparvoli, Daniela, Elisabeth Richardson, Hiroko Osakada, et al. "Remodeling the Specificity of an Endosomal CORVET Tether Underlies Formation of Regulated Secretory Vesicles in the Ciliate Tetrahymena thermophila." Current Biology 28, no. 5 (2018): 697–710. http://dx.doi.org/10.1016/j.cub.2018.01.047.

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28

Lachmann, Jens, Francis A. Barr, and Christian Ungermann. "The Msb3/Gyp3 GAP controls the activity of the Rab GTPases Vps21 and Ypt7 at endosomes and vacuoles." Molecular Biology of the Cell 23, no. 13 (2012): 2516–26. http://dx.doi.org/10.1091/mbc.e11-12-1030.

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Fusion of organelles in the endomembrane system depends on Rab GTPases that interact with tethering factors before lipid bilayer mixing. In yeast, the Rab5 GTPase Vps21 controls fusion and membrane dynamics between early and late endosomes. Here we identify Msb3/Gyp3 as a specific Vps21 GTPase-activating protein (GAP). Loss of Msb3 results in an accumulation of Vps21 and one of its effectors Vps8, a subunit of the CORVET complex, at the vacuole membrane in vivo. In agreement, Msb3 forms a specific transition complex with Vps21, has the highest activity of all recombinant GAPs for Vps21 in vitr

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29

Kvalvaag, Audun Sverre, Sascha Pust, and Kirsten Sandvig. "Vps11, a subunit of the tethering complexes HOPS and CORVET, is involved in regulation of glycolipid degradation and retrograde toxin transport." Communicative & Integrative Biology 7, no. 2 (2014): e28129. http://dx.doi.org/10.4161/cib.28129.

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30

Epp, Nadine, and Christian Ungermann. "The N-Terminal Domains of Vps3 and Vps8 Are Critical for Localization and Function of the CORVET Tethering Complex on Endosomes." PLoS ONE 8, no. 6 (2013): e67307. http://dx.doi.org/10.1371/journal.pone.0067307.

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31

Dove, Stephen K., Kangzhen Dong, Takafumi Kobayashi, Fay K. Williams, and Robert H. Michell. "Phosphatidylinositol 3,5-bisphosphate and Fab1p/PIKfyve underPPIn endo-lysosome function." Biochemical Journal 419, no. 1 (2009): 1–13. http://dx.doi.org/10.1042/bj20081950.

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PtdIns(3,5)P2 is one of the seven regulatory PPIn (polyphosphoinositides) that are ubiquitous in eukaryotes. It controls membrane trafficking at multiple points in the endosomal/lysosomal system and consequently regulates the size, shape and acidity of at least one endo-lysosomal compartment. PtdIns(3,5)P2 appears to exert this control via multiple effector proteins, with each effector specific for a subset of the various PtdIns(3,5)P2-dependent processes. Some putative PtdIns(3,5)P2 effectors have been identified, including Atg18p-related PROPPIN [β-propeller(s) that bind PPIn] proteins and t

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32

Pawelec, Agnes, Janja Arsić, and Ralf Kölling. "Mapping of Vps21 and HOPS Binding Sites in Vps8 and Effect of Binding Site Mutants on Endocytic Trafficking." Eukaryotic Cell 9, no. 4 (2010): 602–10. http://dx.doi.org/10.1128/ec.00286-09.

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ABSTRACT Vps8 is a subunit of the CORVET tethering complex, which is involved in early-to-late endosome fusion. Here, we examine the role of Vps8 in membrane fusion at late endosomes in Saccharomyces cerevisiae. We demonstrate that Vps8 associates with membranes and that this association is independent of the class C/HOPS core complex and, contrary to a previous report, also independent of the Rab GTPase Vps21. Our data indicate that Vps8 makes multiple contacts with membranes. One of these membrane binding regions could be mapped to the N-terminal part of the protein. By two-hybrid analysis,

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33

Chen, Yong, Fan Zhou, Shenshen Zou, et al. "A Vps21 endocytic module regulates autophagy." Molecular Biology of the Cell 25, no. 20 (2014): 3166–77. http://dx.doi.org/10.1091/mbc.e14-04-0917.

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In autophagy, the double-membrane autophagosome delivers cellular components for their degradation in the lysosome. The conserved Ypt/Rab GTPases regulate all cellular trafficking pathways, including autophagy. These GTPases function in modules that include guanine-nucleotide exchange factor (GEF) activators and downstream effectors. Rab7 and its yeast homologue, Ypt7, in the context of such a module, regulate the fusion of both late endosomes and autophagosomes with the lysosome. In yeast, the Rab5-related Vps21 is known for its role in early- to late-endosome transport. Here we show an addit

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34

Lobingier, Braden T., and Alexey J. Merz. "Sec1/Munc18 protein Vps33 binds to SNARE domains and the quaternary SNARE complex." Molecular Biology of the Cell 23, no. 23 (2012): 4611–22. http://dx.doi.org/10.1091/mbc.e12-05-0343.

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Soluble N-ethylmaleimide–sensitive factor attachment protein receptor (SNARE) proteins catalyze membrane fusion events in the secretory and endolysosomal systems, and all SNARE-mediated fusion processes require cofactors of the Sec1/Munc18 (SM) family. Vps33 is an SM protein and subunit of the Vps-C complexes HOPS (homotypic fusion and protein sorting) and CORVET (class C core vacuole/endosome tethering), which are central regulators of endocytic traffic. Here we present biochemical studies of interactions between Saccharomyces cerevisiae vacuolar SNAREs and the HOPS holocomplex or Vps33 alone

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35

Boehm, Cordula, and Mark C. Field. "Evolution of late steps in exocytosis: conservation, specialization." Wellcome Open Research 4 (July 26, 2019): 112. http://dx.doi.org/10.12688/wellcomeopenres.15142.1.

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Background: The eukaryotic endomembrane system likely arose via paralogous expansion of genes encoding proteins specifying organelle identity, coat complexes and government of fusion specificity. While the majority of these gene families were established by the time of the last eukaryotic common ancestor (LECA), subsequent evolutionary events molded these systems, likely reflecting adaptations retained for increased fitness. As well as sequence evolution, these adaptations include loss of otherwise canonical subunits, emergence of lineage-specific proteins and paralog expansion. The exocyst co

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36

Boehm, Cordula, and Mark C. Field. "Evolution of late steps in exocytosis: conservation and specialization of the exocyst complex." Wellcome Open Research 4 (November 29, 2019): 112. http://dx.doi.org/10.12688/wellcomeopenres.15142.2.

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Background: The eukaryotic endomembrane system most likely arose via paralogous expansions of genes encoding proteins that specify organelle identity, coat complexes and govern fusion specificity. While the majority of these gene families were established by the time of the last eukaryotic common ancestor (LECA), subsequent evolutionary events has moulded these systems, likely reflecting adaptations retained for increased fitness. As well as sequence evolution, these adaptations include loss of otherwise canonical components, the emergence of lineage-specific proteins and paralog expansion. Th

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37

Markley, V. J., and J. A. N. Shepperd. "Corset Supply and the Hastings Corset Shop." British Journal of Occupational Therapy 53, no. 4 (1990): 155–57. http://dx.doi.org/10.1177/030802269005300410.

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38

May, Conrad. "The Corset." Journal of Graduate Medical Education 12, no. 4 (2020): 503. http://dx.doi.org/10.4300/jgme-d-19-00751.1.

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39

Feldman, Joel J. "Corset Platysmaplasty." Clinics in Plastic Surgery 19, no. 2 (1992): 369–82. http://dx.doi.org/10.1016/s0094-1298(20)30921-4.

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40

Feldman, Joel J. "Corset Platysmaplasty." Plastic and Reconstructive Surgery 85, no. 3 (1990): 333–43. http://dx.doi.org/10.1097/00006534-199003000-00001.

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41

Hirshowitz, Bernard. "CORSET PLATYSMAPLASTY." Plastic and Reconstructive Surgery 87, no. 1 (1991): 196. http://dx.doi.org/10.1097/00006534-199101000-00050.

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42

Philips, David M., Douglas R. LaBrecque, and Siroos S. Shirazi. "Corset Liver." Journal of Clinical Gastroenterology 7, no. 4 (1985): 361–68. http://dx.doi.org/10.1097/00004836-198508000-00019.

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43

&NA;. "IBUTILIDE (CORVERT)." American Journal of Nursing 97, no. 4 (1997): 59–60. http://dx.doi.org/10.1097/00000446-199704000-00037.

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44

Acevedo, Edwin, Kumar S. Nadhan, Marc Everett, Alexander Moya, and James P. Bradley. "Corset Trunkplasty." Plastic and Reconstructive Surgery 141, no. 1 (2018): 60–69. http://dx.doi.org/10.1097/prs.0000000000003988.

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45

Itoi, Takamasa, Shuji Kawata, Yoshiyuki Fukuda, and Saori Maejima. "Effect of a Corset on the Gait of Healthy Beagle Dogs." Animals 11, no. 9 (2021): 2650. http://dx.doi.org/10.3390/ani11092650.

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The prognosis for intervertebral disc disease (IVDD), a common neurologic disease in dogs, varies, with some cases requiring long-term rehabilitation. Corsets are used as part of the physical rehabilitation of dogs, and one of these, the Anifull Dog’s Corset Pro, is manufactured and sold by Daiya Industry Co., Ltd. This corset is used to relieve pain caused by spinal cord and vertebral diseases, and to prevent neurological conditions from worsening, by limiting spinal movement. However, the effect of the Anifull Dog’s Corset Pro on gait has not yet been clarified. Therefore, we aimed to evalua

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46

Hagino, Ryan T., R. James Valentine, and G. Patrick Clagett. "Aortic corset syndrome." Journal of Vascular Surgery 26, no. 1 (1997): 138–41. http://dx.doi.org/10.1016/s0741-5214(97)70158-7.

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47

Harwood, Elain. "Moreton Corbet Castle." English Heritage Historical Review 1, no. 1 (2006): 37–45. http://dx.doi.org/10.1179/175201606797188499.

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48

Thornton, Susie. "The Susie Corset." Physiotherapy 79, no. 12 (1993): 876. http://dx.doi.org/10.1016/s0031-9406(10)60149-6.

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49

Dito, Giuseppe, and Daniel Sternheimer. "Jean-Claude Cortet." Letters in Mathematical Physics 82, no. 2-3 (2007): 105–6. http://dx.doi.org/10.1007/s11005-007-0210-y.

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50

Taiar, Redha, Alexandra Mitton, Julien Cambier, et al. "Biomechanics of the immediate impact of wearing a rigid thoracolumbar corset on gait kinematics and spatiotemporal parameters." MATEC Web of Conferences 145 (2018): 04007. http://dx.doi.org/10.1051/matecconf/201814504007.

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The corset support is a device classified as orthosis. It compensates a functional deficiency with means of protection, recovery, correction, maintenance, and support or contention. There are two types of orthosis 1) rest orthosis and 2) corrective orthosis. Rest orthosis maintains joints in a defined position to avoid deformities or to relieve a pain at joints. Corrective orthosis adjusts joint deformity either passively or actively. Corset is used in various pathological use, thoracic-lumbar fracture, scoliosis, Scheuermann’s disease or spinal dystrophy. The purpose of this study was 1) to d

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