You have full text access to this OnlineOpen article

Intermediate Organelles of the Plant Secretory Pathway: Identity and Function

Ombretta Foresti,
Jürgen Denecke^*

Article first published online: 9 JUL 2008

DOI: 10.1111/j.1600-0854.2008.00791.x

Issue

Traffic

Volume 9, Issue 10, pages 1599–1612, October 2008

Additional Information

How to Cite

Foresti, O. and Denecke, J. (2008), Intermediate Organelles of the Plant Secretory Pathway: Identity and Function. Traffic, 9: 1599–1612. doi: 10.1111/j.1600-0854.2008.00791.x

Author Information

Centre for Plant Sciences, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK

^* *Jürgen Denecke, j.denecke@leeds.ac.uk

Publication History

Issue published online: 15 SEP 2008
Article first published online: 9 JUL 2008
Received 26 June 2008, revised and accepted for publication 2 July 2008, uncorrected manuscript published online 9 July 2008, published online 4 August 2008

ARTICLE TOOLS

View Full Article (HTML) Get PDF (234K)

References

1
Dacks JB, Poon PP, Field MC. Phylogeny of endocytic components yields insight into the process of nonendosymbiotic organelle evolution. Proc Natl Acad Sci U S A 2008;105:588–593.
2
Bonifacino JS, Glick BS. The mechanisms of vesicle budding and fusion. Cell 2004;116:153–166.
3
Conner SD, Schmid SL. Regulated portals of entry into the cell. Nature 2003;422:37–44.
4
Gruenberg J, Van Der Goot FG. Mechanisms of pathogen entry through the endosomal compartments. Nat Rev Mol Cell Biol 2006;7:495–504.
5
Pelham HR, Roberts LM, Lord JM. Toxin entry: how reversible is the secretory pathway? Trends Cell Biol 1992;2:183–185.
- CrossRef,
- PubMed,
- CAS
6
Maxfield FR, McGraw TE. Endocytic recycling. Nat Rev Mol Cell Biol 2004;5:121–132.
7
Sanderfoot AA, Ahmed SU, Marty-Mazars D, Rapoport I, Kirchhausen T, Marty F, Raikhel NV. A putative vacuolar cargo receptor partially colocalizes with AtPEP12p on a prevacuolar compartment in Arabidopsis roots. Proc Natl Acad Sci U S A 1998;95:9920–9925.
8
Jurgens G. Membrane trafficking in plants. Annu Rev Cell Dev Biol 2004;20:481–504.
9
Boevink P, Oparka K, Santa Cruz S, Martin B, Betteridge A, Hawes C. Stacks on tracks: the plant Golgi apparatus traffics on an actin/ER network. Plant J 1998;15:441–447.
Direct Link:
10
Tolley N, Sparkes IA, Hunter PR, Craddock CP, Nuttall J, Roberts LM, Hawes C, Pedrazzini E, Frigerio L. Overexpression of a plant reticulon remodels the lumen of the cortical endoplasmic reticulum but does not perturb protein transport. Traffic 2008;9:94–102.
Direct Link:
11
Hepler PK, Palevitz BA, Lancelle SA, Mccauley MM, Lichtscheidl I. Cortical endoplasmic-reticulum in plants. J Cell Sci 1990;96:355–373.
- CAS,
- Web of Science® Times Cited: 128
12
Perrin R, Wilkerson C, Keegstra K. Golgi enzymes that synthesize plant cell wall polysaccharides: finding and evaluating candidates in the genomic era. Plant Mol Biol 2001;47:115–130.
13
DaSilva LL, Snapp EL, Denecke J, Lippincott-Schwartz J, Hawes C, Brandizzi F. Endoplasmic reticulum export sites and Golgi bodies behave as single mobile secretory units in plant cells. Plant Cell 2004;16:1753–1771.
14
Bhattacharyya D, Glick BS. Two mammalian Sec16 homologues have nonredundant functions in endoplasmic reticulum (ER) export and transitional ER organization. Mol Biol Cell 2007;18:839–849.
15
Iinuma T, Shiga A, Nakamoto K, O’Brien MB, Aridor M, Arimitsu N, Tagaya M, Tani K. Mammalian Sec16/p250 plays a role in membrane traffic from the endoplasmic reticulum. J Biol Chem 2007;282:17632–17639.
16
Watson P, Townley AK, Koka P, Palmer KJ, Stephens DJ. Sec16 defines endoplasmic reticulum exit sites and is required for secretory cargo export in mammalian cells. Traffic 2006;7:1678–1687.
Direct Link:
17
Fath S, Mancias JD, Bi X, Goldberg J. Structure and organization of coat proteins in the COPII cage. Cell 2007;129:1325–1336.
18
Kirchhausen T. Making COPII coats. Cell 2007;129:1251–1252.
19
Aridor M, Fish KN, Bannykh S, Weissman J, Roberts TH, Lippincott-Schwartz J, Balch WE. The Sar1 GTPase coordinates biosynthetic cargo selection with endoplasmic reticulum export site assembly. J Cell Biol 2001;152:213–229.
20
Barlowe C. Signals for COPII-dependent export from the ER: what’s the ticket out? Trends Cell Biol 2003;13:295–300.
21
Cai H, Yu S, Menon S, Cai Y, Lazarova D, Fu C, Reinisch K, Hay JC, Ferro-Novick S. TRAPPI tethers COPII vesicles by binding the coat subunit Sec23. Nature 2007;445:941–944.
22
Barlowe C. Coupled ER to Golgi transport reconstituted with purified cytosolic proteins. J Cell Biol 1997;139:1097–1108.
23
Kurihara T, Hamamoto S, Gimeno RE, Kaiser CA, Schekman R, Yoshihisa T. Sec24p and Iss1p function interchangeably in transport vesicle formation from the endoplasmic reticulum in Saccharomyces cerevisiae. Mol Biol Cell 2000;11:983–998.
24
Hanton SL, Chatre L, Renna L, Matheson LA, Brandizzi F. De novo formation of plant endoplasmic reticulum export sites is membrane cargo induced and signal mediated. Plant Physiol 2007;143:1640–1650.
25
Forster R, Weiss M, Zimmermann T, Reynaud EG, Verissimo F, Stephens DJ, Pepperkok R. Secretory cargo regulates the turnover of COPII subunits at single ER exit sites. Curr Biol 2006;16:173–179.
26
Yang YD, Elamawi R, Bubeck J, Pepperkok R, Ritzenthaler C, Robinson DG. Dynamics of COPII vesicles and the Golgi apparatus in cultured Nicotiana tabacum BY-2 cells provides evidence for transient association of Golgi stacks with endoplasmic reticulum exit sites. Plant Cell 2005;17:1513–1531.
27
Hawes C, Satiat-Jeunemaitre B. The plant Golgi apparatus – going with the flow. Biochim Biophys Acta 2005;1744:466–480.
- CrossRef,
- PubMed
28
Hawes C, Osterrieder A, Hummel E, Sparkes I. The plant ER-Golgi interface. Traffic 2008. doi: 10.1111/j.1600-0854.2008.00773.x.
Direct Link:
29
Robinson DG, Herranz MC, Bubeck J, Pepperkok R, Ritzenthaler C. Membrane dynamics in the early secretory pathway. Crit Rev Plant Sci 2007;26:199–225.
30
Hara-Nishimura II, Shimada T, Hatano K, Takeuchi Y, Nishimura M. Transport of storage proteins to protein storage vacuoles is mediated by large precursor-accumulating vesicles. Plant Cell 1998;10:825–836.
31
Toyooka K, Okamoto T, Minamikawa T. Mass transport of proform of a KDEL-tailed cysteine proteinase (SH-EP) to protein storage vacuoles by endoplasmic reticulum-derived vesicle is involved in protein mobilization in germinating seeds. J Cell Biol 2000;148:453–464.
32
Phillipson BA, Pimpl P, DaSilva LL, Crofts AJ, Taylor JP, Movafeghi A, Robinson DG, Denecke J. Secretory bulk flow of soluble proteins is efficient and COPII dependent. Plant Cell 2001;13:2005–2020.
33
Pimpl P, Taylor JP, Snowden C, Hillmer S, Robinson DG, Denecke J. Golgi-mediated vacuolar sorting of the endoplasmic reticulum chaperone BiP may play an active role in quality control within the secretory pathway. Plant Cell 2006;18:198–211.
34
Tormakangas K, Hadlington JL, Pimpl P, Hillmer S, Brandizzi F, Teeri TH, Denecke J. A vacuolar sorting domain may also influence the way in which proteins leave the endoplasmic reticulum. Plant Cell 2001;13:2021–2032.
35
Bentley M, Liang Y, Mullen K, Xu D, Sztul E, Hay JC. SNARE status regulates tether recruitment and function in homotypic COPII vesicle fusion. J Biol Chem 2006;281:38825–38833.
36
Xu D, Hay JC. Reconstitution of COPII vesicle fusion to generate a pre-Golgi intermediate compartment. J Cell Biol 2004;167:997–1003.
37
Martinez-Menarguez JA, Geuze HJ, Slot JW, Klumperman J. Vesicular tubular clusters between the ER and Golgi mediate concentration of soluble secretory proteins by exclusion from COPI-coated vesicles. Cell 1999;98:81–90.
38
Appenzeller-Herzog C, Hauri HP. The ER-Golgi intermediate compartment (ERGIC): in search of its identity and function. J Cell Sci 2006;119:2173–2183.
39
Pimpl P, Movafeghi A, Coughlan S, Denecke J, Hillmer S, Robinson DG. In situ localization and in vitro induction of plant COPI-coated vesicles. Plant Cell 2000;12:2219–2236.
40
Lee MC, Miller EA, Goldberg J, Orci L, Schekman R. Bi-directional protein transport between the ER and Golgi. Annu Rev Cell Dev Biol 2004;20:87–123.
41
Crofts AJ, Leborgne-Castel N, Hillmer S, Robinson DG, Phillipson B, Carlsson LE, Ashford DA, Denecke J. Saturation of the endoplasmic reticulum retention machinery reveals anterograde bulk flow. Plant Cell 1999;11:2233–2248.
42
Hanton SL, Renna L, Bortolotti LE, Chatre L, Stefano G, Brandizzi F. Diacidic motifs influence the export of transmembrane proteins from the endoplasmic reticulum in plant cells. Plant Cell 2005;17:3081–3093.
43
Geldner N. The plant endosomal system – its structure and role in signal transduction and plant development. Planta 2004;219:547–560.
44
Ritzenthaler C, Nebenfuhr A, Movafeghi A, Stussi-Garaud C, Behnia L, Pimpl P, Staehelin LA, Robinson DG. Reevaluation of the effects of brefeldin A on plant cells using tobacco Bright Yellow 2 cells expressing Golgi-targeted green fluorescent protein and COPI antisera. Plant Cell 2002;14:237–261.
45
Richter S, Geldner N, Schrader J, Wolters H, Stierhof YD, Rios G, Koncz C, Robinson DG, Jurgens G. Functional diversification of closely related ARF-GEFs in protein secretion and recycling. Nature 2007;448:488–492.
46
Teh OK, Moore I. An ARF-GEF acting at the Golgi and in selective endocytosis in polarized plant cells. Nature 2007;448:493–496.
47
Langhans M, Marcote MJ, Pimpl P, Virgili-Lopez G, Robinson DG, Aniento F. In vivo trafficking and localization of p24 proteins in plant cells. Traffic 2008;9:770–785.
Direct Link:
48
Pimpl P, Hanton SL, Taylor JP, Pinto-daSilva LL, Denecke J. The GTPase ARF1p controls the sequence-specific vacuolar sorting route to the lytic vacuole. Plant Cell 2003;15:1242–1256.
49
Stefano G, Renna L, Chatre L, Hanton SL, Moreau P, Hawes C, Brandizzi F. In tobacco leaf epidermal cells, the integrity of protein export from the endoplasmic reticulum and of ER export sites depends on active COPI machinery. Plant J 2006;46:95–110.
Direct Link:
50
Boulaflous A, Faso C, Brandizzi F. Deciphering the Golgi apparatus: from imaging to genes. Traffic 2008. doi:10.1111/j.1600-0854.2008.00769.x.
Direct Link:
51
Li L, Shimada T, Takahashi H, Ueda H, Fukao Y, Kondo M, Nishimura M, Hara-Nishimura I. MAIGO2 is involved in exit of seed storage proteins from the endoplasmic reticulum in Arabidopsis thaliana. Plant Cell 2006;18:3535–3547.
52
Cosson P, Schroder-Kohne S, Sweet DS, Demolliere C, Hennecke S, Frigerio G, Letourneur F. The Sec20/Tip20p complex is involved in ER retrieval of dilysine-tagged proteins. Eur J Cell Biol 1997;73:93–97.
53
Frigerio G. The Saccharomyces cerevisiae early secretion mutant tip20 is synthetic lethal with mutants in yeast coatomer and the SNARE proteins Sec22p and Ufe1p. Yeast 1998;14:633–646.
Direct Link:
54
Kraynack BA, Chan A, Rosenthal E, Essid M, Umansky B, Waters MG, Schmitt HD. Dsl1p, Tip20p, and the novel Dsl3(Sec39) protein are required for the stability of the Q/t-SNARE complex at the endoplasmic reticulum in yeast. Mol Biol Cell 2005;16:3963–3977.
55
Kamena F, Spang A. Tip20p prohibits back-fusion of COPII vesicles with the endoplasmic reticulum. Science 2004;304:286–289.
56
Hanton SL, Brandizzi F. Fluorescent proteins as markers in the plant secretory pathway. Microsc Res Tech 2006;69:152–159.
Direct Link:
57
Robinson DG, Oliviusson P, Hinz G. Protein sorting to the storage vacuoles of plants: a critical appraisal. Traffic 2005;6:615–625.
Direct Link:
58
Vitale A, Hinz G. Sorting of proteins to storage vacuoles: how many mechanisms? Trends Plant Sci 2005;10:316–323.
59
Paris N, Stanley CM, Jones RL, Rogers JC. Plant cells contain two functionally distinct vacuolar compartments. Cell 1996;85:563–572.
60
Otegui MS, Herder R, Schulze J, Jung R, Staehelin LA. The proteolytic processing of seed storage proteins in Arabidopsis embryo cells starts in the multivesicular bodies. Plant Cell 2006;18:2567–2581.
61
Hunter PR, Craddock CP, Di Benedetto S, Roberts LM, Frigerio L. Fluorescent reporter proteins for the tonoplast and the vacuolar lumen identify a single vacuolar compartment in Arabidopsis cells. Plant Physiol 2007;145:1371–1382.
62
Shimada T, Fuji K, Tamura K, Kondo M, Nishimura M, Hara-Nishimura I. Vacuolar sorting receptor for seed storage proteins in Arabidopsis thaliana. Proc Natl Acad Sci U S A 2003;100:16095–16100.
63
Olbrich A, Hillmer S, Hinz G, Oliviusson P, Robinson DG. Newly formed vacuoles in root meristems of barley and pea seedlings have characteristics of both protein storage and lytic vacuoles. Plant Physiol 2007;145:1383–1394.
64
Robinson DG. Response to rogers letter. Plant Physiol 2008;146:1026.
65
Frigerio L. Response to rogers letter. Plant Physiol 2008;146:1026–1027.
66
Frigerio L, Hinz G, Robinson DG. Multiple vacuoles in plant cells: rule or exception? Traffic 2008. doi: 10.1111/j.1600-0854.2008.00776.x.
Direct Link:
67
Hillmer S, Movafeghi A, Robinson DG, Hinz G. Vacuolar storage proteins are sorted in the cis-cisternae of the pea cotyledon Golgi apparatus. J Cell Biol 2001;152:41–50.
68
Park M, Kim SJ, Vitale A, Hwang I. Identification of the protein storage vacuole and protein targeting to the vacuole in leaf cells of three plant species. Plant Physiol 2004;134:625–639.
69
Park M, Lee D, Lee GJ, Hwang I. AtRMR1 functions as a cargo receptor for protein trafficking to the protein storage vacuole. J Cell Biol 2005;170:757–767.
70
Hinz G, Colanesi S, Hillmer S, Rogers JC, Robinson DG. Localization of vacuolar transport receptors and cargo proteins in the Golgi apparatus of developing Arabidopsis embryos. Traffic 2007;8:1452–1464.
Direct Link:
71
Pelletier L, Stern CA, Pypaert M, Sheff D, Ngo HM, Roper N, He CY, Hu K, Toomre D, Coppens I, Roos DS, Joiner KA, Warren G. Golgi biogenesis in Toxoplasma gondii. Nature 2002;418:548–552.
72
Bevis BJ, Hammond AT, Reinke CA, Glick BS. De novo formation of transitional ER sites and Golgi structures in Pichia pastoris. Nat Cell Biol 2002;4:750–756.
73
Glick BS. Can the Golgi form de novo? Nat Rev Mol Cell Biol 2002;3:615–619.
74
Radulescu AE, Siddhanta A, Shields D. A role for clathrin in reassembly of the Golgi apparatus. Mol Biol Cell 2007;18:94–105.
75
Langhans M, Hawes C, Hillmer S, Hummel E, Robinson DG. Golgi regeneration after brefeldin A treatment in BY-2 cells entails stack enlargement and cisternal growth followed by division. Plant Physiol 2007;145:527–538.
76
Xu J, Scheres B. Dissection of Arabidopsis ADP-RIBOSYLATION FACTOR 1 function in epidermal cell polarity. Plant Cell 2005;17:525–536.
77
Matheson LA, Hanton SL, Rossi M, Latijnhouwers M, Stefano G, Renna L, Brandizzi F. Multiple roles of ADP-ribosylation factor 1 in plant cells include spatially regulated recruitment of coatomer and elements of the Golgi matrix. Plant Physiol 2007;143:1615–1627.
78
Matheson LA, Suri SS, Hanton SL, Chatre L, Brandizzi F. Correct targeting of plant ARF GTPases relies on distinct protein domains. Traffic 2008;9:103–120.
Direct Link:
79
Manolea F, Claude A, Chun J, Rosas J, Melancon P. Distinct functions for Arf nucleotide exchange factors at the Golgi complex: GBF1 and BIGs are required for assembly and maintenance of the Golgi stack and TGN, respectively. Mol Biol Cell 2007;19:523–535.
80
Geldner N, Anders N, Wolters H, Keicher J, Kornberger W, Muller P, Delbarre A, Ueda T, Nakano A, Jurgens G. The Arabidopsis GNOM ARF-GEF mediates endosomal recycling, auxin transport, and auxin-dependent plant growth. Cell 2003;112:219–230.
81
Uemura T, Ueda T, Ohniwa RL, Nakano A, Takeyasu K, Sato MH. Systematic analysis of SNARE molecules in Arabidopsis: dissection of the post-Golgi network in plant cells. Cell Struct Funct 2004;29:49–65.
82
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;20:101–123.
83
Dettmer J, Hong-Hermesdorf A, Stierhof YD, Schumacher K. Vacuolar H+ -ATPase activity is required for endocytic and secretory trafficking in Arabidopsis. Plant Cell 2006;18:715–730.
84
Lam SK, Siu CL, Hillmer S, Jang S, An G, Robinson DG, Jiang L. Rice SCAMP1 defines clathrin-coated, trans-golgi-located tubular-vesicular structures as an early endosome in tobacco BY-2 cells. Plant Cell 2007;19:296–319.
85
Kirsch T, Paris N, Butler JM, Beevers L, Rogers JC. Purification and initial characterization of a potential plant vacuolar targeting receptor. Proc Natl Acad Sci U S A 1994;91:3403–3407.
86
Hinz G, Hillmer S, Baumer M, Hohl II. Vacuolar storage proteins and the putative vacuolar sorting receptor BP-80 exit the golgi apparatus of developing pea cotyledons in different transport vesicles. Plant Cell 1999;11:1509–1524.
87
Li YB, Rogers SW, Tse YC, Lo SW, Sun SS, Jauh GY, Jiang L. BP-80 and homologs are concentrated on post-Golgi, probable lytic prevacuolar compartments. Plant Cell Physiol 2002;43:726–742.
88
Tse YC, Mo B, Hillmer S, Zhao M, Lo SW, Robinson DG, Jiang L. Identification of multivesicular bodies as prevacuolar compartments in Nicotiana tabacum BY-2 cells. Plant Cell 2004;16:672–693.
89
Happel N, Honing S, Neuhaus JM, Paris N, Robinson DG, Holstein SE. Arabidopsis mu A-adaptin interacts with the tyrosine motif of the vacuolar sorting receptor VSR-PS1. Plant J 2004;37:678–693.
Direct Link:
90
Hillmer S, Freundt H, Robinson DG. The partially coated reticulum and its relationship to the Golgi-apparatus in higher-plant cells. Eur J Cell Biol 1988;47:206–212.
- Web of Science® Times Cited: 50
91
Pesacreta TC, Lucas WJ. Presence of a partially-coated reticulum in Angiosperms. Protoplasma 1985;125:173–184.
- CrossRef,
- Web of Science® Times Cited: 68
92
Staehelin LA, Moore I. The plant Golgi-apparatus – structure, functional-organization and trafficking mechanisms. Annu Rev Plant Physiol Plant Mol Biol 1995;46:261–288.
93
Pesacreta TC, Lucas WJ. Plasma membrane coat and a coated vesicle-associated reticulum of membranes: their structure and possible interrelationship in Chara corallina. J Cell Biol 1984;98:1537–1545.
94
Lam SK, Tse YC, Robinson DG, Jiang L. Tracking down the elusive early endosome. Trends Plant Sci 2007;12:497–505.
95
Tanchak MA, Rennie PJ, Fowke LC. Ultrastructure of the partially coated reticulum and dictyosomes during endocytosis by soybean protoplasts. Planta 1988;175:433–441.
- CrossRef,
- Web of Science® Times Cited: 43
96
Tanchak MA, Griffing LR, Mersey BG, Fowke LC. Endocytosis of cationized ferritin by coated vesicles of soybean protoplasts. Planta 1984;162:481–486.
97
Tanchak MA, Fowke LC. The morphology of multivesicular bodies in soybean protoplasts and their role in endocytosis. Protoplasma 1987;138:173–182.
- CrossRef,
- Web of Science® Times Cited: 64
98
Hillmer S, Depta H, Robinson DG. Confirmation of endocytosis in higher-plant protoplasts using lectin-gold conjugates. Eur J Cell Biol 1986;41:142–149.
- Web of Science® Times Cited: 67
99
Joachim S, Robinson DG. Endocytosis of cationic ferritin by bean leaf protoplasts. Eur J Cell Biol 1984;34:212–216.
100
Meckel T, Hurst AC, Thiel G, Homann U. Endocytosis against high turgor: intact guard cells of Vicia faba constitutively endocytose fluorescently labelled plasma membrane and GFP-tagged K-channel KAT1. Plant J 2004;39:182–193.
Direct Link:
101
Meckel T, Hurst AC, Thiel G, Homann U. Guard cells undergo constitutive and pressure-driven membrane turnover. Protoplasma 2005;226:23–29.
102
Samaj J, Read ND, Volkmann D, Menzel D, Baluska F. The endocytic network in plants. Trends Cell Biol 2005;15:425–433.
103
Bolte S, Talbot C, Boutte Y, Catrice O, Read ND, Satiat-Jeunemaitre B. FM-dyes as experimental probes for dissecting vesicle trafficking in living plant cells. J Microsc 2004;214:159–173.
Direct Link:
104
Ueda T, Uemura T, Sato MH, Nakano A. Functional differentiation of endosomes in Arabidopsis cells. Plant J 2004;40:783–789.
Direct Link:
105
Ueda T, Yamaguchi M, Uchimiya H, Nakano A. Ara6, a plant-unique novel type Rab GTPase, functions in the endocytic pathway of Arabidopsis thaliana. EMBO J 2001;20:4730–4741.
106
Lee GJ, Sohn EJ, Lee MH, Hwang I. The Arabidopsis rab5 homologs rha1 and ara7 localize to the prevacuolar compartment. Plant Cell Physiol 2004;45:1211–1220.
107
Kotzer AM, Brandizzi F, Neumann U, Paris N, Moore I, Hawes C. AtRabF2b (Ara7) acts on the vacuolar trafficking pathway in tobacco leaf epidermal cells. J Cell Sci 2004;117:6377–6389.
108
Bolte S, Brown S, Satiat-Jeunemaitre B. The N-myristoylated Rab-GTPase m-Rabmc is involved in post-Golgi trafficking events to the lytic vacuole in plant cells. J Cell Sci 2004;117:943–954.
109
Haas TJ, Sliwinski MK, Martinez DE, Preuss M, Ebine K, Ueda T, Nielsen E, Odorizzi G, Otegui MS. The Arabidopsis AAA ATPase SKD1 is involved in multivesicular endosome function and interacts with its positive regulator LYST-INTERACTING PROTEIN5. Plant Cell 2007;19:1295–1312.
110
Van Ijzendoorn SC. Recycling endosomes. J Cell Sci 2006;119:1679–1681.
111
Reichardt I, Stierhof YD, Mayer U, Richter S, Schwarz H, Schumacher K, Jurgens G. Plant cytokinesis requires de novo secretory trafficking but not endocytosis. Curr Biol 2007;17:2047–2053.
112
Denecke J, Carlsson LE, Vidal S, Hoglund AS, Ek B, Van Zeijl MJ, Sinjorgo KM, Palva ET. The tobacco homolog of mammalian calreticulin is present in protein complexes in vivo. Plant Cell 1995;7:391–406.
113
Robert S, Chary SN, Drakakaki G, Li S, Yang Z, Raikhel NV, Hicks GR. Endosidin 1 defines a compartment involved in endocytosis of the brassinosteroid receptor BRI1 and the auxin transporters PIN2 and AUX1. Proc Natl Acad Sci U S A 2008;105:8464–8469.
114
Bar M, Aharon M, Benjamin S, Rotblat B, Horowitz M, Avni A. AtEHDs, novel Arabidopsis EH-domain containing proteins involved in endocytosis. Plant J 2008. doi: 10.1111/j.1365-313X.2008.03571.x.
Direct Link:
115
Tamura K, Takahashi H, Kunieda T, Fuji K, Shimada T, Hara-Nishimura I. Arabidopsis KAM2/GRV2 is required for proper endosome formation and functions in vacuolar sorting and determination of the embryo growth axis. Plant Cell 2007;19:320–332.
116
Silady RA, Ehrhardt DW, Jackson K, Faulkner C, Oparka K, Somerville CR. The GRV2/RME-8 protein of Arabidopsis functions in the late endocytic pathway and is required for vacuolar membrane flow. Plant J 2008;53:29–41.
Direct Link:
117
Men S, Boutte Y, Ikeda Y, Li X, Palme K, Stierhof YD, Hartmann MA, Moritz T, Grebe M. Sterol-dependent endocytosis mediates post-cytokinetic acquisition of PIN2 auxin efflux carrier polarity. Nat Cell Biol 2008;10:237–244.
118
Lisboa S, Scherer GEF, Quader H. Localized endocytosis in tobacco pollen tubes: visualisation and dynamics of membrane retrieval by a fluorescent phospholipid. Plant Cell Rep 2008;27:21–28.
119
Zonia L, Munnik T. Vesicle trafficking dynamics and visualization of zones of exocytosis and endocytosis in tobacco pollen tubes. J Exp Bot 2008;59:861–873.
120
Paris N, Neuhaus JM. BP-80 as a vacuolar sorting receptor. Plant Mol Biol 2002;50:903–914.
121
Park JH, Oufattole M, Rogers JC. Golgi-mediated vacuolar sorting in plant cells: RMR proteins are sorting receptors for the protein aggregation/membrane internalization pathway. Plant Sci 2007;172:728–745.
122
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;17:132–148.
123
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;18:1477–1497.
124
Oliviusson P, Heinzerling O, Hillmer S, Hinz G, Tse YC, Jiang L, Robinson DG. Plant retromer, localized to the prevacuolar compartment and microvesicles in Arabidopsis, may interact with vacuolar sorting receptors. Plant Cell 2006;18:1239–1252.
125
Jaillais Y, Fobis-Loisy I, Miege C, Rollin C, Gaude T. AtSNX1 defines an endosome for auxin-carrier trafficking in Arabidopsis. Nature 2006;443:106–109.
126
Shimada T, Koumoto Y, Li L, Yamazaki M, Kondo M, Nishimura M, Hara-Nishimura I. AtVPS29, a putative component of a retromer complex, is required for the efficient sorting of seed storage proteins. Plant Cell Physiol 2006;47:1187–1194.
127
Yamazaki M, Shimada T, Takahashi H, Tamura K, Kondo M, Nishimura M, Hara-Nishimura I. Arabidopsis VPS35, a retromer component, is required for vacuolar protein sorting and involved in plant growth and leaf senescence. Plant Cell Physiol 2008;49:142–156.
128
Jaillais Y, Santambrogio M, Rozier F, Fobis-Loisy I, Miege C, Gaude T. The retromer protein VPS29 links cell polarity and organ initiation in plants. Cell 2007;130:1057–1070.
129
Winter V, Hauser MT. Exploring the ESCRTing machinery in eukaryotes. Trends Plant Sci 2006;11:115–123.
130
Russell MR, Nickerson DP, Odorizzi G. Molecular mechanisms of late endosome morphology, identity and sorting. Curr Opin Cell Biol 2006;18:422–428.
131
Van Der Goot FG, Gruenberg J. Intra-endosomal membrane traffic. Trends Cell Biol 2006;16:514–521.
132
Jaillais Y, Fobis-Loisy I, Miege C, Gaude T. Evidence for a sorting endosome in Arabidopsis root cells. Plant J 2008;53:237–247.
Direct Link:
133
Saito C, Ueda T, Abe H, Wada Y, Kuroiwa T, Hisada A, Furuya M, Nakano A. A complex and mobile structure forms a distinct subregion within the continuous vacuolar membrane in young cotyledons of Arabidopsis. Plant J 2002;29:245–255.
Direct Link:
134
Gomez L, Chrispeels MJ. Tonoplast and soluble vacuolar proteins are targeted by different mechanisms. Plant Cell 1993;5:1113–1124.
135
Matsuoka K, Bassham DC, Raikhel NV, Nakamura K. Different sensitivity to wortmannin of two vacuolar sorting signals indicates the presence of distinct sorting machineries in tobacco cells. J Cell Biol 1995;130:1307–1318.
136
Kirsch T, Saalbach G, Raikhel NV, Beevers L. Interaction of a potential vacuolar targeting receptor with amino- and carboxyl-terminal targeting determinants. Plant Physiol 1996;111:469–474.
137
Kim DH, Eu YJ, Yoo CM, Kim YW, Pih KT, Jin JB, Kim SJ, Stenmark H, Hwang I. Trafficking of phosphatidylinositol 3-phosphate from the trans-Golgi network to the lumen of the central vacuole in plant cells. Plant Cell 2001;13:287–301.
138
Shimada T, Kuroyanagi M, Nishimura M, Hara-Nishimura I. A pumpkin 72-kDa membrane protein of precursor-accumulating vesicles has characteristics of a vacuolar sorting receptor. Plant Cell Physiol 1997;38:1414–1420.
139
Shimada T, Watanabe E, Tamura K, Hayashi Y, Nishimura M, Hara-Nishimura I. A vacuolar sorting receptor PV72 on the membrane of vesicles that accumulate precursors of seed storage proteins (PAC vesicles). Plant Cell Physiol 2002;43:1086–1095.
140
Watanabe E, Shimada T, Kuroyanagi M, Nishimura M, Hara-Nishimura I. Calcium-mediated association of a putative vacuolar sorting receptor PV72 with a propeptide of 2S albumin. J Biol Chem 2002;277:8708–8715.
141
Watanabe E, Shimada T, Tamura K, Matsushima R, Koumoto Y, Nishimura M, Hara-Nishimura I. An ER-localized form of PV72, a seed-specific vacuolar sorting receptor, interferes the transport of an NPIR-containing proteinase in Arabidopsis leaves. Plant Cell Physiol 2004;45:9–17.
142
Jolliffe NA, Brown JC, Neumann U, Vicre M, Bachi A, Hawes C, Ceriotti A, Roberts LM, Frigerio L. Transport of ricin and 2S albumin precursors to the storage vacuoles of Ricinus communis endosperm involves the Golgi and VSR-like receptors. Plant J 2004;39:821–833.
Direct Link:
143
Craddock CP, Hunter PR, Szakacs E, Hinz G, Robinson DG, Frigerio L. Lack of a vacuolar sorting receptor leads to non-specific missorting of soluble vacuolar proteins in Arabidopsis seeds. Traffic 2008;9:408–416.
Direct Link:
144
Epimashko S, Meckel T, Fischer-Schliebs E, Luttge U, Thiel G. Two functionally different vacuoles for static and dynamic purposes in one plant mesophyll leaf cell. Plant J 2004;37:294–300.
145
Vitale A, Ceriotti A. Protein quality control mechanisms and protein storage in the endoplasmic reticulum. A conflict of interests? Plant Physiol 2004;136:3420–3426.
146
Harsay E, Schekman R. A subset of yeast vacuolar protein sorting mutants is blocked in one branch of the exocytic pathway. J Cell Biol 2002;156:271–285.
147
Harsay E, Schekman R. Avl9p, a member of a novel protein superfamily, functions in the late secretory pathway. Mol Biol Cell 2007;18:1203–1219.
148
He B, Xi F, Zhang J, TerBush D, Zhang X, Guo W. Exo70p mediates the secretion of specific exocytic vesicles at early stages of the cell cycle for polarized cell growth. J Cell Biol 2007;176:771–777.
149
D’Angelo G, Polishchuk E, Di Tullio G, Santoro M, Di Campli A, Godi A, West G, Bielawski J, Chuang CC, Van Der Spoel AC, Platt FM, Hannun YA, Polishchuk R, Mattjus P, De Matteis MA. Glycosphingolipid synthesis requires FAPP2 transfer of glucosylceramide. Nature 2007;449:62–67.
150
Leucci MR, Di Sansebastiano GP, Gigante M, Dalessandro G, Piro G. Secretion marker proteins and cell-wall polysaccharides move through different secretory pathways. Planta 2007;225:1001–1017.
151
Foresti O, Dasilva LL, Denecke J. Overexpression of the Arabidopsis syntaxin PEP12/SYP21 inhibits transport from the prevacuolar compartment to the lytic vacuole in vivo. Plant Cell 2006;18:2275–2293.
152
Matsuura-Tokita K, Takeuchi M, Ichihara A, Mikuriya K, Nakano A. Live imaging of yeast Golgi cisternal maturation. Nature 2006;441:1007–1010.
153
Zheng H, Kunst L, Hawes C, Moore I. A GFP-based assay reveals a role for RHD3 in transport between the endoplasmic reticulum and Golgi apparatus. Plant J 2004;37:398–414.
Direct Link:

View Full Article (HTML) Get PDF (234K)

JOURNAL TOOLS

JOURNAL MENU

FIND ISSUES

FIND ARTICLES

GET ACCESS

FOR CONTRIBUTORS

ABOUT THIS JOURNAL

SPECIAL FEATURES

Intermediate Organelles of the Plant Secretory Pathway: Identity and Function

Traffic

How to Cite

Author Information

Publication History

ARTICLE TOOLS

References

More content like this

JOURNAL TOOLS

JOURNAL MENU

FIND ISSUES

FIND ARTICLES

GET ACCESS

FOR CONTRIBUTORS

ABOUT THIS JOURNAL

SPECIAL FEATURES

Intermediate Organelles of the Plant Secretory Pathway: Identity and Function

Traffic

How to Cite

Author Information

Publication History

SEARCH

SEARCH BY CITATION

ARTICLE TOOLS

References

More content like this