Determinants of GPI-PLC Localisation to the Flagellum and Access to GPI-Anchored Substrates in Trypanosomes
In Trypanosoma brucei, glycosylphosphatidylinositol phospholipase C (GPI-PLC) is a virulence factor that releases variant surface glycoprotein (VSG) from dying cells. In live cells, GPI-PLC is localised to the plasma membrane where it is concentrated on the flagellar membrane, so activity or access must be tightly regulated as very little VSG is shed. Little is known about regulation except that acylation within a short internal motif containing three cysteines is necessary for GPI-PLC to access VSG in dying cells. Here, GPI-PLC mutants have been analysed both for subcellular localisation and for the ability to release VSG from dying cells. Two sequence determinants necessary for concentration on the flagellar membrane were identified. First, all three cysteines are required for full concentration on the flagellar membrane. Mutants with two cysteines localise predominantly to the plasma membrane but lose some of their flagellar concentration, while mutants with one cysteine are mainly localised to membranes between the nucleus and flagellar pocket. Second, a proline residue close to the C-terminus, and distant from the acylated cysteines, is necessary for concentration on the flagellar membrane. The localisation of GPI-PLC to the plasma but not flagellar membrane is necessary for access to the VSG in dying cells. Cellular structures necessary for concentration on the flagellar membrane were identified by depletion of components. Disruption of the flagellar pocket collar caused loss of concentration whereas detachment of the flagellum from the cell body after disruption of the flagellar attachment zone did not. Thus, targeting to the flagellar membrane requires: a titratable level of acylation, a motif including a proline, and a functional flagellar pocket. These results provide an insight into how the segregation of flagellar membrane proteins from those present in the flagellar pocket and cell body membranes is achieved.
Vyšlo v časopise:
Determinants of GPI-PLC Localisation to the Flagellum and Access to GPI-Anchored Substrates in Trypanosomes. PLoS Pathog 9(8): e32767. doi:10.1371/journal.ppat.1003566
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.ppat.1003566
Souhrn
In Trypanosoma brucei, glycosylphosphatidylinositol phospholipase C (GPI-PLC) is a virulence factor that releases variant surface glycoprotein (VSG) from dying cells. In live cells, GPI-PLC is localised to the plasma membrane where it is concentrated on the flagellar membrane, so activity or access must be tightly regulated as very little VSG is shed. Little is known about regulation except that acylation within a short internal motif containing three cysteines is necessary for GPI-PLC to access VSG in dying cells. Here, GPI-PLC mutants have been analysed both for subcellular localisation and for the ability to release VSG from dying cells. Two sequence determinants necessary for concentration on the flagellar membrane were identified. First, all three cysteines are required for full concentration on the flagellar membrane. Mutants with two cysteines localise predominantly to the plasma membrane but lose some of their flagellar concentration, while mutants with one cysteine are mainly localised to membranes between the nucleus and flagellar pocket. Second, a proline residue close to the C-terminus, and distant from the acylated cysteines, is necessary for concentration on the flagellar membrane. The localisation of GPI-PLC to the plasma but not flagellar membrane is necessary for access to the VSG in dying cells. Cellular structures necessary for concentration on the flagellar membrane were identified by depletion of components. Disruption of the flagellar pocket collar caused loss of concentration whereas detachment of the flagellum from the cell body after disruption of the flagellar attachment zone did not. Thus, targeting to the flagellar membrane requires: a titratable level of acylation, a motif including a proline, and a functional flagellar pocket. These results provide an insight into how the segregation of flagellar membrane proteins from those present in the flagellar pocket and cell body membranes is achieved.
Zdroje
1. CrossGA (1975) Identification, purification and properties of clone-specific glycoprotein antigens constituting the surface coat of Trypanosoma brucei. Parasitology 71: 393–417.
2. JacksonDG, OwenMJ, VoorheisHP (1985) A new method for the rapid purification of both the membrane-bound and released forms of the variant surface glycoprotein from Trypanosoma brucei. Biochem J 230: 195–202.
3. PalA, HallBS, JeffriesTR, FieldMC (2003) Rab5 and Rab11 mediate transferrin and anti-variant surface glycoprotein antibody recycling in Trypanosoma brucei. Biochem J 374: 443–451.
4. MansfieldJM, PaulnockDM (2005) Regulation of innate and acquired immunity in African trypanosomiasis. Parasite Immunol 27: 361–371.
5. EngstlerM, PfohlT, HerminghausS, BoshartM, WiegertjesG, et al. (2007) Hydrodynamic flow-mediated protein sorting on the cell surface of trypanosomes. Cell 131: 505–515.
6. SmithTK, VasilevaN, GluenzE, TerryS, PortmanN, et al. (2009) Blocking variant surface glycoprotein synthesis in Trypanosoma brucei triggers a general arrest in translation initiation. PLoS ONE 4: e7532.
7. FergusonMAJ, HomansSW, DwekRA, RademacherTW (1988) Glycosyl-Phosphatidylinositol Moiety That Anchors Trypanosoma-Brucei Variant Surface Glycoprotein to the Membrane. Science 239: 753–759.
8. BulowR, OverathP (1986) Purification and characterization of the membrane-form variant surface glycoprotein hydrolase of Trypanosoma brucei. J Biol Chem 261: 11918–11923.
9. FoxJA, DuszenkoM, FergusonMA, LowMG, CrossGA (1986) Purification and characterization of a novel glycan-phosphatidylinositol-specific phospholipase C from Trypanosoma brucei. J Biol Chem 261: 15767–15771.
10. HereldD, KrakowJL, BangsJD, HartGW, EnglundPT (1986) A phospholipase C from Trypanosoma brucei which selectively cleaves the glycolipid on the variant surface glycoprotein. J Biol Chem 261: 13813–13819.
11. Mensa-WilmotK, EnglundPT (1992) Glycosyl phosphatidylinositol-specific phospholipase C of Trypanosoma brucei: expression in Escherichia coli. Mol Biochem Parasitol 56: 311–321.
12. BulowR, NonnengasserC, OverathP (1989) Release of the variant surface glycoprotein during differentiation of bloodstream to procyclic forms of Trypanosoma brucei. Mol Biochem Parasitol 32: 85–92.
13. SeyfangA, MeckeD, DuszenkoM (1990) Degradation, recycling, and shedding of Trypanosoma brucei variant surface glycoprotein. J Protozool 37: 546–552.
14. WebbH, CarnallN, VanhammeL, RolinS, Van Den AbbeeleJ, et al. (1997) The GPI-phospholipase C of Trypanosoma brucei is nonessential but influences parasitemia in mice. J Cell Biol 139: 103–114.
15. CarringtonM, CarnallN, CrowMS, GaudA, RedpathMB, et al. (1998) The properties and function of the glycosylphosphatidylinositol-phospholipase C in Trypanosoma brucei. Mol Biochem Parasitol 91: 153–164.
16. HereldD, HartGW, EnglundPT (1988) cDNA encoding the glycosyl-phosphatidylinositol-specific phospholipase C of Trypanosoma brucei. Proc Natl Acad Sci U S A 85: 8914–8918.
17. CarringtonM, BulowR, ReinkeH, OverathP (1989) Sequence and expression of the glycosyl-phosphatidylinositol-specific phospholipase C of Trypanosoma brucei. Mol Biochem Parasitol 33: 289–296.
18. Paturiaux-HanocqF, Hanocq-QuertierJ, de AlmeidaML, NolanDP, PaysA, et al. (2000) A role for the dynamic acylation of a cluster of cysteine residues in regulating the activity of the glycosylphosphatidylinositol-specific phospholipase C of Trypanosoma brucei. J Biol Chem 275: 12147–12155.
19. ArmahDA, Mensa-WilmotK (1999) S-myristoylation of a glycosylphosphatidylinositol-specific phospholipase C in Trypanosoma brucei. J Biol Chem 274: 5931–5938.
20. HanrahanO, WebbH, O'ByrneR, BrabazonE, TreumannA, et al. (2009) The glycosylphosphatidylinositol-PLC in Trypanosoma brucei forms a linear array on the exterior of the flagellar membrane before and after activation. PLoS Pathog 5: e1000468.
21. LacombleS, VaughanS, GadelhaC, MorphewMK, ShawMK, et al. (2009) Three-dimensional cellular architecture of the flagellar pocket and associated cytoskeleton in trypanosomes revealed by electron microscope tomography. J Cell Sci 122: 1081–1090.
22. LeeMG, BihainBE, RussellDG, DeckelbaumRJ, Van der PloegLH (1990) Characterization of a cDNA encoding a cysteine-rich cell surface protein located in the flagellar pocket of the protozoan Trypanosoma brucei. Mol Cell Biol 10: 4506–4517.
23. EmmerBT, SoutherC, TorielloKM, OlsonCL, EptingCL, et al. (2009) Identification of a palmitoyl acyltransferase required for protein sorting to the flagellar membrane. J Cell Sci 122: 867–874.
24. FieldMC, CarringtonM (2004) Intracellular membrane transport systems in Trypanosoma brucei. Traffic 5: 905–913.
25. BonhiversM, NowackiS, LandreinN, RobinsonDR (2008) Biogenesis of the trypanosome endo-exocytotic organelle is cytoskeleton mediated. PLoS Biol 6: e105.
26. OberholzerM, LangousisG, NguyenHT, SaadaEA, ShimogawaMM, et al. (2011) Independent analysis of the flagellum surface and matrix proteomes provides insight into flagellum signaling in mammalian-infectious Trypanosoma brucei. Mol Cell Proteomics 10: M111 010538.
27. GodselLM, EngmanDM (1999) Flagellar protein localization mediated by a calcium-myristoyl/palmitoyl switch mechanism. EMBO J 18: 2057–2065.
28. TamBM, MoritzOL, HurdLB, PapermasterDS (2000) Identification of an outer segment targeting signal in the COOH terminus of rhodopsin using transgenic Xenopus laevis. J Cell Biol 151: 1369–1380.
29. TaoB, BuS, YangZ, SirokyB, KappesJC, et al. (2009) Cystin localizes to primary cilia via membrane microdomains and a targeting motif. J Am Soc Nephrol 20: 2570–2580.
30. FollitJA, LiL, VucicaY, PazourGJ (2010) The cytoplasmic tail of fibrocystin contains a ciliary targeting sequence. J Cell Biol 188: 21–28.
31. HolderAA, CrossGA (1981) Glycopeptides from variant surface glycoproteins of Trypanosoma Brucei. C-terminal location of antigenically cross-reacting carbohydrate moieties. Mol Biochem Parasitol 2: 135–150.
32. Cardoso de AlmeidaML, TurnerMJ (1983) The membrane form of variant surface glycoproteins of Trypanosoma brucei. Nature 302: 349–352.
33. ZamzeSE, FergusonMA, CollinsR, DwekRA, RademacherTW (1988) Characterization of the cross-reacting determinant (CRD) of the glycosyl-phosphatidylinositol membrane anchor of Trypanosoma brucei variant surface glycoprotein. Eur J Biochem 176: 527–534.
34. BangsJD, DoeringTL, EnglundPT, HartGW (1988) Biosynthesis of a variant surface glycoprotein of Trypanosoma brucei. Processing of the glycolipid membrane anchor and N-linked oligosaccharides. J Biol Chem 263: 17697–17705.
35. Cardoso De AlmeidaML, GeuskensM, PaysE (1999) Cell lysis induces redistribution of the GPI-anchored variant surface glycoprotein on both faces of the plasma membrane of Trypanosoma brucei. J Cell Sci 112 (Pt 23) 4461–4473.
36. KellyS, ReedJ, KramerS, EllisL, WebbH, et al. (2007) Functional genomics in Trypanosoma brucei: a collection of vectors for the expression of tagged proteins from endogenous and ectopic gene loci. Mol Biochem Parasitol 154: 103–109.
37. WebbH, BurnsR, EllisL, KimblinN, CarringtonM (2005) Developmentally regulated instability of the GPI-PLC mRNA is dependent on a short-lived protein factor. Nucleic Acids Res 33: 1503–1512.
38. WirtzE, LealS, OchattC, CrossGA (1999) A tightly regulated inducible expression system for conditional gene knock-outs and dominant-negative genetics in Trypanosoma brucei. Mol Biochem Parasitol 99: 89–101.
39. ZiegelbauerK, OverathP (1993) Organization of two invariant surface glycoproteins in the surface coat of Trypanosoma brucei. Infect Immun 61: 4540–4545.
40. DeflorinJ, RudolfM, SeebeckT (1994) The major components of the paraflagellar rod of Trypanosoma brucei are two similar, but distinct proteins which are encoded by two different gene loci. J Biol Chem 269: 28745–28751.
41. KramerS, QueirozR, EllisL, HoheiselJD, ClaytonC, et al. (2010) The RNA helicase DHH1 is central to the correct expression of many developmentally regulated mRNAs in trypanosomes. J Cell Sci 123: 699–711.
42. ChungWL, CarringtonM, FieldMC (2004) Cytoplasmic targeting signals in transmembrane invariant surface glycoproteins of trypanosomes. J Biol Chem 279: 54887–54895.
43. GonzaloS, LinderME (1998) SNAP-25 palmitoylation and plasma membrane targeting require a functional secretory pathway. Mol Biol Cell 9: 585–597.
44. SubramanyaS, ArmahDA, Mensa-WilmotK (2010) Trypanosoma brucei: Reduction of GPI-phospholipase C protein during differentiation is dependent on replication of newly transformed cells. Experimental Parasitology 125: 222–229.
45. CarnallN, WebbH, CarringtonM (1997) Mutagenesis study of the glycosylphosphatidylinositol phospholipase C of Trypanosoma brucei. Mol Biochem Parasitol 90: 423–432.
46. AllenCL, GouldingD, FieldMC (2003) Clathrin-mediated endocytosis is essential in Trypanosoma brucei. EMBO J 22: 4991–5002.
47. WoodsK, Nic a'BhairdN, DooleyC, Perez-MorgaD, NolanDP (2013) Identification and characterization of a stage specific membrane protein involved in flagellar attachment in Trypanosoma brucei. PLoS ONE 8: e52846.
48. BülowR, GriffithsG, WebsterP, StierhofYD, OpperdoesFR, et al. (1989) Intracellular localization of the glycosyl-phosphatidylinositol-specific phospholipase C of Trypanosoma brucei. J Cell Sci 93 (Pt 2) 233–240.
49. ParatMO, FoxPL (2001) Palmitoylation of caveolin-1 in endothelial cells is post-translational but irreversible. J Biol Chem 276: 15776–15782.
50. GreavesJ, ChamberlainLH (2007) Palmitoylation-dependent protein sorting. J Cell Biol 176: 249–254.
51. SalaunC, GreavesJ, ChamberlainLH (2010) The intracellular dynamic of protein palmitoylation. J Cell Biol 191: 1229–1238.
52. RocksO, GerauerM, VartakN, KochS, HuangZP, et al. (2010) The palmitoylation machinery is a spatially organizing system for peripheral membrane proteins. Cell 141: 458–471.
53. GreavesJ, GorlekuOA, SalaunC, ChamberlainLH (2010) Palmitoylation of the SNAP25 protein family: specificity and regulation by DHHC palmitoyl transferases. J Biol Chem 285: 24629–24638.
54. GreavesJ, ChamberlainLH (2011) Differential palmitoylation regulates intracellular patterning of SNAP25. J Cell Sci 124: 1351–1360.
55. GrandgenettPM, OtsuK, WilsonHR, WilsonME, DonelsonJE (2007) A function for a specific zinc metalloprotease of African trypanosomes. PLoS Pathog 3: 1432–1445.
56. MaricD, McGwireBS, BuchananKT, OlsonCL, EmmerBT, et al. (2011) Molecular determinants of ciliary membrane localization of Trypanosoma cruzi flagellar calcium-binding protein. J Biol Chem 286: 33109–33117.
57. TranKD, Rodriguez-ContrerasD, ShindeU, LandfearSM (2012) Both sequence and context are important for flagellar targeting of a glucose transporter. J Cell Sci 125: 3293–3298.
58. BroadheadR, DaweHR, FarrH, GriffithsS, HartSR, et al. (2006) Flagellar motility is required for the viability of the bloodstream trypanosome. Nature 440: 224–227.
59. HuQC, MilenkovicL, JinH, ScottMP, NachuryMV, et al. (2010) A Septin Diffusion Barrier at the Base of the Primary Cilium Maintains Ciliary Membrane Protein Distribution. Science 329: 436–439.
60. CraigeB, TsaoCC, DienerDR, HouYQ, LechtreckKF, et al. (2010) CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content. Journal of Cell Biology 190: 927–940.
61. McCullochR (2004) Antigenic variation in African trypanosomes: monitoring progress. Trends Parasitol 20: 117–121.
62. ZiegelbauerK, OverathP (1992) Identification of invariant surface glycoproteins in the bloodstream stage of Trypanosoma brucei. J Biol Chem 267: 10791–10796.
63. BangsJD, UyetakeL, BrickmanMJ, BalberAE, BoothroydJC (1993) Molecular cloning and cellular localization of a BiP homologue in Trypanosoma brucei. Divergent ER retention signals in a lower eukaryote. J Cell Sci 105 (Pt 4) 1101–1113.
64. KohlL, SherwinT, GullK (1999) Assembly of the paraflagellar rod and the flagellum attachment zone complex during the Trypanosoma brucei cell cycle. J Eukaryot Microbiol 46: 105–109.
Štítky
Hygiena a epidemiológia Infekčné lekárstvo LaboratóriumČlánok vyšiel v časopise
PLOS Pathogens
2013 Číslo 8
- Očkování proti virové hemoragické horečce Ebola experimentální vakcínou rVSVDG-ZEBOV-GP
- Parazitičtí červi v terapii Crohnovy choroby a dalších zánětlivých autoimunitních onemocnění
- Koronavirus hýbe světem: Víte jak se chránit a jak postupovat v případě podezření?
Najčítanejšie v tomto čísle
- Host Immune Response to Intestinal Amebiasis
- Bed Bugs and Infectious Disease: A Case for the Arboviruses
- Discovery of Anthelmintic Drug Targets and Drugs Using Chokepoints in Nematode Metabolic Pathways
- Relevance of Trehalose in Pathogenicity: Some General Rules, Yet Many Exceptions