Annexin C4 in A. Fumigatus: A proteomics approach to understand the function

Journal of Proteomics

Volumn 74, Issue 10, 2011, Pages 1950-1958

  Khalaj, Vahid ^a   Azarian, Bahareh ^a   Enayati, Somayeh ^a   Vaziri, Behrouz ^a  

^a PASTEUR INSTITUTE OF IRAN   (Iran)

Author keywords

A. fumigatus; AnnexinC4; Oxidative stress; Proteomics

Indexed keywords

ANNEXIN; PROTEIN ANNEXIN C4; UNCLASSIFIED DRUG;

ARTICLE; ASPERGILLUS FUMIGATUS; FUNGAL STRAIN; OXIDATIVE STRESS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEOMICS; RESPIRATORY CHAIN; SPOROGENESIS; STRESS;

ANNEXINS; ASPERGILLUS FUMIGATUS; ELECTRON TRANSPORT; FUNGAL PROTEINS; OXIDATIVE STRESS;

ASPERGILLUS FUMIGATUS; FUNGI;

EID: 80052036558     PISSN: 18743919     EISSN: 18767737     Source Type: Journal    
DOI: 10.1016/j.jprot.2011.05.018     Document Type: Article

References (36)

1. Geisow M.J. Common domain structure of Ca2+ and lipid-binding proteins. FEBS Lett 1986, 203:99-103.
2. Geisow M.J., Fritsche U., Hexham J.M., Dash B., Johnson T. A consensus amino-acid sequence repeat in Torpedo and mammalian Ca2+-dependent membrane-binding proteins. Nature 1986, 320:636-638.
3. Gerke V., Moss S.E. Annexins: from structure to function. Physiol Rev 2002, 82:331-371.
4. Moss S.E., Morgan R.O. The annexins. Genome Biol 2004, 5:219.
5. Khalaj V., Smith L., Brookman J., Tuckwell D. Identification of a novel class of annexin genes. FEBS Lett 2004, 562:79-86.
6. Rescher U., Gerke V. Annexins-unique membrane binding proteins with diverse functions. J Cell Sci 2004, 117:2631-2639.
7. Khalaj V., Hey P., Smith L., Robson G.D., Brookman J. The Aspergillus niger annexin, anxC3.1 is constitutively expressed and is not essential for protein secretion. FEMS Microbiol Lett 2004, 239:163-169.
8. Moller E.M., Bahnweg G., Sandermann H., Geiger H.H. A simple and efficient protocol for isolation of high molecular weight DNA from filamentous fungi, fruit bodies, and infected plant tissues. Nucleic Acids Res 1992, 20:6115-6116.
9. Sambrook J., Russell D. Molecular cloning: a laboratory manual 2001, Cold spring Harbor laboratory press, NY.
10. Punt P.J., Oliver R.P., Dingemanse M.A., Pouwels P.H., van den Hondel C.A. Transformation of Aspergillus based on the hygromycin B resistance marker from Escherichia coli. Gene 1987, 56:117-124.
11. Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal biochem 1976, 72:248-254.
12. Candiano G., Bruschi M., Musante L., Santucci L., Ghiggeri G.M., Carnemolla B., et al. Blue silver: a very sensitive colloidal Coomassie G-250 staining for proteome analysis. Electrophoresis 2004, 25:1327-1333.
13. Romano J., Nimrod G., Ben-Tal N., Shadkchan Y., Baruch K., Sharon H., et al. Disruption of the Aspergillus fumigatus ECM33 homologue results in rapid conidial germination, antifungal resistance and hypervirulence. Microbiology 2006, 152:1919-1928.
14. Vodisch M., Albrecht D., Lessing F., Schmidt A.D., Winkler R., Guthke R., et al. Two-dimensional proteome reference maps for the human pathogenic filamentous fungus Aspergillus fumigatus. Proteomics 2009, 9:1407-1415.
15. Bruneau J.M., Magnin T., Tagat E., Legrand R., Bernard M., Diaquin M., et al. Proteome analysis of Aspergillus fumigatus identifies glycosylphosphatidylinositol-anchored proteins associated to the cell wall biosynthesis. Electrophoresis 2001, 22:2812-2823.
16. Norbeck J., Blomberg A. The level of cAMP-dependent protein kinase A activity strongly affects osmotolerance and osmo-instigated gene expression changes in Saccharomyces cerevisiae. Yeast 2000, 16:121-137.
17. Zhao W., Panepinto J.C., Fortwendel J.R., Fox L., Oliver B.G., Askew D.S., et al. Deletion of the regulatory subunit of protein kinase A in Aspergillus fumigatus alters morphology, sensitivity to oxidative damage, and virulence. Infect Immun 2006, 74:4865-4874.
18. Godon C., Lagniel G., Lee J., Buhler J.M., Kieffer S., Perrot M., et al. The H2O2 stimulon in Saccharomyces cerevisiae. J Biol Chem 1998, 273:22480-22489.
19. Juhnke H., Krems B., Kotter P., Entian K.D. Mutants that show increased sensitivity to hydrogen peroxide reveal an important role for the pentose phosphate pathway in protection of yeast against oxidative stress. Mol Gen Genet 1996, 252:456-464.
20. Thorpe G.W., Fong C.S., Alic N., Higgins V.J., Dawes I.W. Cells have distinct mechanisms to maintain protection against different reactive oxygen species: oxidative-stress-response genes. Proc Natl Acad Sci U S A 2004, 101:6564-6569.
21. Shimizu M., Fujii T., Masuo S., Fujita K., Takaya N. Proteomic analysis of Aspergillus nidulans cultured under hypoxic conditions. Proteomics 2009, 9:7-19.
22. Bommer U.A., Thiele B.J. The translationally controlled tumour protein (TCTP). Int J Biochem Cell Biol 2004, 36:379-385.
23. Gnanasekar M., Dakshinamoorthy G., Ramaswamy K. Translationally controlled tumor protein is a novel heat shock protein with chaperone-like activity. Biochem Biophys Res Commun 2009, 386:333-337.
24. Rid R., Onder K., Trost A., Bauer J., Hintner H., Ritter M., et al. H(2)O(2)-dependent translocation of TCTP into the nucleus enables its interaction with VDR in human keratinocytes: TCTP as a further module in calcitriol signalling. J Steroid Biochem Mol Biol 2009.
25. Nagano-Ito M., Banba A., Ichikawa S. Functional cloning of genes that suppress oxidative stress-induced cell death: TCTP prevents hydrogen peroxide-induced cell death. FEBS Lett 2009, 583:1363-1367.
26. Reverberi M., Zjalic S., Ricelli A., Punelli F., Camera E., Fabbri C., et al. Modulation of antioxidant defense in Aspergillus parasiticus is involved in aflatoxin biosynthesis: a role for the ApyapA gene. Eukaryot Cell 2008, 7:988-1000.
27. Li N., Brun T., Cnop M., Cunha D.A., Eizirik D.L., Maechler P. Transient oxidative stress damages mitochondrial machinery inducing persistent beta-cell dysfunction. J Biol Chem 2009, 284:23602-23612.
28. Raha S., Robinson B.H. Mitochondria, oxygen free radicals, disease and ageing. Trends Biochem Sci 2000, 25:502-508.
29. Zuin A., Gabrielli N., Calvo I.A., Garcia-Santamarina S., Hoe K.L., Kim D.U., et al. Mitochondrial dysfunction increases oxidative stress and decreases chronological life span in fission yeast. PLoS One 2008, 3:e2842.
30. Gasch A.P., Spellman P.T., Kao C.M., Carmel-Harel O., Eisen M.B., Storz G., et al. Genomic expression programs in the response of yeast cells to environmental changes. Mol Biol Cell 2000, 11:4241-4257.
31. Chen Q., Ding Q., Thorpe J., Dohmen R.J., Keller J.N. RNA interference toward UMP1 induces proteasome inhibition in Saccharomyces cerevisiae: evidence for protein oxidation and autophagic cell death. Free Radic Biol Med 2005, 38:226-234.
32. Monastyrskaya K., Babiychuk E.B., Draeger A. The annexins: spatial and temporal coordination of signaling events during cellular stress. Cell Mol Life Sci 2009, 66:2623-2642.
33. Jami S.K., Clark G.B., Turlapati S.A., Handley C., Roux S.J., Kirti P.B. Ectopic expression of an annexin from Brassica juncea confers tolerance to abiotic and biotic stress treatments in transgenic tobacco. Plant Physiol Biochem 2008, 46:1019-1030.
34. Konopka-Postupolska D., Clark G., Goch G., Debski J., Floras K., Cantero A., et al. The role of annexin 1 in drought stress in Arabidopsis. Plant Physiol 2009, 150:1394-1410.
35. Gorecka K.M., Konopka-Postupolska D., Hennig J., Buchet R., Pikula S. Peroxidase activity of annexin 1 from Arabidopsis thaliana. Biochem Biophys Res Commun 2005, 336:868-875.
36. Mortimer J.C., Coxon K.M., Laohavisit A., Davies J.M. Heme-independent soluble and membrane-associated peroxidase activity of a Zea mays annexin preparation. Plant Signal Behav 2009, 4:428-430.