Routes to and from the plasma membrane: bulk flow versus signal mediated endocytosis

References

• Reyes FC, Buono R, Otegui MS. Plant endosomal trafficking pathways. Curr Opin Plant Biol 2011; 14:666-73; PMID:21821464; http://dx.doi.org/10.1016/j.pbi.2011.07.009
   PubMed Web of Science ®Google Scholar
• An Q, Hückelhoven R, Kogel KH, van Bel AJ. Multivesicular bodies participate in a cell wall-associated defence response in barley leaves attacked by the pathogenic powdery mildew fungus. Cell Microbiol 2006; 8:1009-19; PMID:16681841
   PubMed Web of Science ®Google Scholar
• Regente M, Pinedo M, Elizalde M, de la Canal L. Apoplastic exosome-like vesicles: a new way of protein secretion in plants? Plant Signal Behav 2012; 7:544-6; PMID:22516827; http://dx.doi.org/10.4161/psb.19675
   PubMedGoogle Scholar
• Drakakaki G, Dandekar A. Protein secretion: how many secretory routes does a plant cell have? Plant Sci 2013; 203-4:74-8; PMID:23415330; http://dx.doi.org/10.1016/j.plantsci.2012.12.017
   PubMed Web of Science ®Google Scholar
• De Marcos Lousa C, Gershlick DC, Denecke J. Mechanisms and concepts paving the way towards a complete transport cycle of plant vacuolar sorting receptors. Plant Cell 2012; 24:1714-32; PMID:22570446; http://dx.doi.org/10.1105/tpc.112.095679
   PubMed Web of Science ®Google Scholar
• Gershlick DC, de Marcos Lousa C., Foresti O, Lee AJ, Pereira EA, daSilva LL, Bottanelli F, Denecke J. Golgi-dependent transport of vacuolar sorting receptors is regulated by COPII, AP1, and AP4 protein complexes in tobacco. Plant Cell 2014; 26:1308-29; PMID:24642936; http://dx.doi.org/10.1105/tpc.113.122226
   PubMed Web of Science ®Google Scholar
• daSilva LL, Foresti O, Denecke J. Targeting of the plant vacuolar sorting receptor BP80 is dependent on multiple sorting signals in the cytosolic tail. Plant Cell 2006; 18:1477-97; PMID:16714388; http://dx.doi.org/10.1105/tpc.105.040394
   PubMed Web of Science ®Google Scholar
• Foresti O, Gershlick DC, Bottanelli F, Hummel E, Hawes C, Denecke J. A recycling-defective vacuolar sorting receptor reveals an intermediate compartment situated between prevacuoles and vacuoles in tobacco. Plant Cell 2010; 22:3992-4008; PMID:21177482; http://dx.doi.org/10.1105/tpc.110
   PubMed Web of Science ®Google Scholar
• daSilva LL, Taylor JP, Hadlington JL, Hanton SL, Snowden CJ, Fox SJ, Foresti O, Brandizzi F, Denecke J. Receptor salvage from the prevacuolar compartment is essential for efficient vacuolar protein targeting. Plant Cell 2005; 17:132-48; PMID:15632053; http://dx.doi.org/10.1105/tpc.104.026351
   PubMed Web of Science ®Google Scholar
• Saint-Jean B, Seveno-Carpentier E, Alcon C, Neuhaus JM, Paris N. The cytosolic tail dipeptide Ile-Met of the pea receptor BP80 is required for recycling from the prevacuole and for endocytosis. Plant Cell 2010; 22:2825-37; PMID:20807880; http://dx.doi.org/10.1105/tpc.109.072215
   PubMed Web of Science ®Google Scholar
• Park M, Song K, Reichardt I, Kim H, Mayer U, Stierhof YD, Hwang I, Jürgens G. Arabidopsis μ-adaptin subunit AP1M of adaptor protein complex 1 mediates late secretory and vacuolar traffic and is required for growth. Proc Natl Acad Sci USA 2013; 110:10318-23; PMID:23733933; http://dx.doi.org/10.1073/pnas.1300460110
   PubMed Web of Science ®Google Scholar
• Denecke J, Botterman J, Deblaere R. Protein secretion in plant cells can occur via a default pathway. Plant Cell 1990; 2:51-9; PMID:1967050; http://dx.doi.org/10.1105/tpc.2.1.51
   PubMed Web of Science ®Google Scholar
• Brandizzi F, Frangne N, Marc-Martin S, Hawes C, Neuhaus JM, Paris N. The destination for single-pass membrane proteins is influenced markedly by the length of the hydrophobic domain. Plant Cell 2002; 14:1077-92; PMID:12034898; http://dx.doi.org/10.1105/tpc.000620
   PubMed Web of Science ®Google Scholar
• Langhans M, Marcote MJ, Pimpl P, Virgili-López G, Robinson DG, Aniento F. In vivo trafficking and localization of p24 proteins in plant cells. Traffic 2008; 9:770-85; PMID:18266912; http://dx.doi.org/10.1111/j.1600-0854.2008.00719.x
   PubMed Web of Science ®Google Scholar
• Mercanti V, Marchetti A, Lelong E, Perez F, Orci L, Cosson P. Transmembrane domains control exclusion of membrane proteins from clathrin-coated pits. J Cell Sci 2010; 123:3329-35; PMID:20826467; http://dx.doi.org/10.1242/jcs.073031
   PubMed Web of Science ®Google Scholar
• Bar M, Avni A. EHD2 inhibits ligand-induced endocytosis and signaling of the leucine-rich repeat receptor-like protein LeEix2. Plant J 2009; 59:600-11; PMID:19392695; http://dx.doi.org/10.1111/j.1365-313X.2009.03897.x
   PubMed Web of Science ®Google Scholar
• Takano J, Tanaka M, Toyoda A, Miwa K, Kasai K, Fuji K, Onouchi H, Naito S, Fujiwara T. Polar localization and degradation of Arabidopsis boron transporters through distinct trafficking pathways. Proc Natl Acad Sci USA 2010; 107:5220-5; PMID:20194745; http://dx.doi.org/10.1073/pnas.0910744107
   PubMedGoogle Scholar
• Scheuring D, Künzl F, Viotti C, Yan MS, Jiang L, Schellmann S, Robinson DG, Pimpl P. Ubiquitin initiates sorting of Golgi and plasma membrane proteins into the vacuolar degradation pathway. BMC Plant Biol 2012; 12:164; PMID:22970698; http://dx.doi.org/10.1186/1471-2229-12-164
   PubMed Web of Science ®Google Scholar
• Katsiarimpa A, Muñoz A, Kalinowska K, Uemura T, Rojo E, Isono E. The ESCRT-III-interacting deubiquitinating enzyme AMSH3 is essential for degradation of ubiquitinated membrane proteins in Arabidopsis thaliana. Plant Cell Physiol 2014; 55:727-36; PMID:24486765; http://dx.doi.org/10.1093/pcp/pcu019
   PubMed Web of Science ®Google Scholar
• Bednarek SY, Reynolds TL, Schroeder M, Grabowski R, Hengst L, Gallwitz D, Raikhel NV. A small GTP-binding protein from Arabidopsis thaliana functionally complements the yeast YPT6 null mutant. Plant Physiol 1994; 104:591-6; PMID:8159788; http://dx.doi.org/10.1104/pp.104.2.591
   PubMed Web of Science ®Google Scholar
• Grigoriev I, Splinter D, Keijzer N, Wulf PS, Demmers J, Ohtsuka T, Modesti M, Maly IV, Grosveld F, Hoogenraad CC, Akhmanova A. Rab6 regulates transport and targeting of exocytotic carriers. Dev Cell 2007; 13:305-14; PMID:17681140; http://dx.doi.org/10.1016/j.devcel.2007.06.010
   PubMed Web of Science ®Google Scholar
• Chow CM, Neto H, Foucart C, Moore I. Rab-A2 and Rab-A3 GTPases define a trans-golgi endosomal membrane domain in Arabidopsis that contributes substantially to the cell plate. Plant Cell 2008; 20:101-23; PMID:18239134; http://dx.doi.org/10.1105/tpc.107.052001
   PubMed Web of Science ®Google Scholar
• Feraru E, Feraru MI, Asaoka R, Paciorek T, De Rycke R, Tanaka H, Nakano A, Friml J. BEX5/RabA1b regulates trans-Golgi network-to-plasma membrane protein trafficking in Arabidopsis. Plant Cell 2012; 24:3074-86; PMID:22773752; http://dx.doi.org/10.1105/tpc.112.098152
   PubMed Web of Science ®Google Scholar
• Choi SW, Tamaki T, Ebine K, Uemura T, Ueda T, Nakano A. RABA members act in distinct steps of subcellular trafficking of the FLAGELLIN SENSING2 receptor. Plant Cell 2013; 25:1174-87; PMID:23532067; http://dx.doi.org/10.1105/tpc.112.108803
   PubMed Web of Science ®Google Scholar