Sorting of soluble proteins in the secretory pathway of plants

Current Opinion in Plant Biology

Volumn 3, Issue 6, 2000, Pages 461-468

  Hadlington, Jane L ^a   Denecke, Jürgen ^a  

^a UNIVERSITY OF LEEDS   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0033709686     PISSN: 13695266     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1369-5266(00)00114-X     Document Type: Review

References (60)

1. Plant vacuoles
2. Protein storage bodies and vacuoles
3. The endoplasmic reticulum - Gateway of the secretory pathway
4. The role of the endoplasmic-reticulum in protein-synthesis, modification and intracellular-transport
5. RD2, a yeast gene required for the receptor-mediated retrieval of luminal ER proteins from the secretory pathway
6. Retrieval of HDEL proteins is required for growth of yeast cells
7. The Arabidopsis endoplasmic-reticulum retention receptor functions in yeast
8. Stacks on tracks: The plant Golgi apparatus traffics on an actin/ER network
9. Plant and mammalian sorting signals for protein retention in the endoplasmic reticulum contain a conserved epitope
10. Protein quality control along the route to the plant vacuole
11. Saturation of the endoplasmic reticulum retention machinery reveals anterograde bulk flow
12. KDEL acts before the Golgi-mediated formation of complex asparagine-linked glycans
13. Protein recycling from the Golgi apparatus to the endoplasmic reticulum in plants and its minor contribution to calreticulin retention
14. Recycling of proteins from the Golgi compartment to the ER in yeast
15. BiP and calreticulin form an abundant complex that is independent of endoplasmic reticulum stress
16. Calreticulin and calnexin in plants
17. A C-terminal signal prevents secretion of luminal ER proteins
18. Calnexin and BiP interact with acid phosphatase independently of glucose trimming and reglucosylation in Schizosaccharomyces pombe
19. Protein secretion in plant-cells can occur via a default pathway
20. The signal peptide of a vacuolar protein is necessary and sufficient for the efficient secretion of a cytosolic protein
21. COPII - A membrane coat formed by sec proteins that drive vesicle budding from the endoplasmic-reticulum
22. In situ localisation and in vitro induction of plant COPI-coated vesicles
23. Sorting of phaseolin to the vacuole is saturable and requires a short C-terminal peptide
24. In vitro mutated phytohemagglutinin genes expressed in tobacco seeds: Role of glycans in protein targeting and stability
25. Expression of mutant patatin protein in transgenic tobacco plants - Role of glycans and intracellular location
26. Role of propeptide glycan in posttranslational processing and transport of barley lectin to vacuoles in transgenic tobacco
27. Evidence for N-terminal and C-terminal processing of a plant defense-related enzyme - Primary structure of tobacco preprobeta-1,3-glucanase
28. A carboxyl-terminal propeptide is necessary for proper sorting of barley lectin to vacuoles of tobacco
29. The barley lectin carboxyl-terminal propeptide is a vacuolar protein sorting determinant in plants
30. Propeptide of a precursor to a plant vacuolar protein required for vacuolar targeting
31. Identification of vacuolar sorting information in phytohemagglutinin, an unprocessed vacuolar protein
32. Different legumin protein domains act as vacuolar targeting signals
33. Proaleurain vacuolar targeting is mediated by short contiguous peptide interactions
34. Cis-elements of protein transport to the plant vacuoles
35. C-terminal pro-peptides and vacuolar sorting by BP80-type proteins: Not all C-terminal propeptides are equal
36. Determination of the functional elements within the vacuolar targeting signal of barley lectin
37. Mutation analysis of the C-terminal vacuolar targeting peptide of tobacco chitinase: Low specificity of the sorting system, and gradual transition between intracellular retention and secretion into the extracellular space
38. Large alkyl side-chains of isoleucine and leucine in the NPIRL region constitute the core of the vacuolar sorting determinant of sporamin precursor
39. Purification and initial characterization of a potential plant vacuolar targeting receptor
40. Structural requirements for ligand binding by a probable plant vacuolar sorting receptor
41. Cloning and subcellular location of an Arabidopsis receptor-like protein that shares common features with protein-sorting receptors of eukaryotic cells
42. Molecular cloning and further characterization of a probable plant vacuolar sorting receptor
43. A pumpkin 72-kDa membrane protein of precursor-accumulating vesicles has characteristics of a vacuolar sorting receptor
44. Identification and characterization of a prevacuolar compartment in stigmas of Nicotiana alata
45. A putative vacuolar cargo receptor partially colocalizes with AtPEP12p on a prevacuolar compartment in Arabidopsis roots
46. The plant vesicle associated SNARE AtVTI1a likely mediates vesicle transport from the trans Golgi network to the prevacuolar compartment
47. The role of BP-80 and homologs in sorting proteins to vacuoles
48. Protein storage vacuoles form de-novo during pea cotyledon development
49. Plant cells contain two functionally distinct vacuolar compartments
50. Tonoplast and soluble vacuolar proteins are targeted by different mechanisms
51. Different sensitivity to Wortmannin of 2 vacuolar sorting signals indicates the presence of distinct sorting machineries in tobacco cells
52. Brefeldin-A effects on tobacco pollen tubes
53. The specificity of vesicle trafficking: Coat proteins and SNAREs
54. Transport of storage proteins to the vacuole is mediated by vesicles without a clathrin coat
55. Vacuolar storage proteins and the putative vacuolar sorting receptor BP-80 exit the Golgi apparatus of developing pea cotyledons in different transport vesicles
56. Evidence for a novel route of wheat storage proteins to vacuoles
57. Transport of storage proteins to protein storage vacuoles is mediated by large precursor-accumulating vesicles
58. Mass transport of preform 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
59. The C-terminal HDEL sequence is sufficient for retention of secretory proteins in the endoplasmic reticulum (ER) but promotes vacuolar targeting of proteins that escape the ER
60. 2-terminal propeptide-containing vacuolar proteins in Arabidopsis thaliana