M. Geisow, and lipid-binding proteins, FEBS Letters, vol.219, issue.1, pp.99-103, 1986.
DOI : 10.1016/0014-5793(86)81445-4

M. Geisow, U. Fritsche, J. Hexham, B. Dash, and T. Johnson, A consensus amino-acid sequence repeat in Torpedo and mammalian Ca2+-dependent membrane-binding proteins, Nature, vol.320, issue.6063, pp.636-644, 1986.
DOI : 10.1038/320636a0

V. Gerke and S. Moss, Annexins: From Structure to Function, Physiological Reviews, vol.82, issue.2, pp.331-71, 2002.
DOI : 10.1152/physrev.00030.2001

S. Moss and R. Morgan, Annexins, Trends in Cell Biology, vol.7, issue.3, p.219, 2004.
DOI : 10.1016/S0962-8924(96)10049-0

V. Khalaj, L. Smith, J. Brookman, and D. Tuckwell, Identification of a novel class of annexin genes, FEBS Letters, vol.53, issue.1-3, pp.79-86, 2004.
DOI : 10.1016/S0014-5793(04)00186-3

U. Rescher and V. Gerke, Annexins - unique membrane binding proteins with diverse functions, Journal of Cell Science, vol.117, issue.13, pp.2631-2640, 2004.
DOI : 10.1242/jcs.01245

V. Khalaj, P. Hey, L. Smith, G. Robson, and J. Brookman, is constitutively expressed and is not essential for protein secretion, FEMS Microbiology Letters, vol.239, issue.1, pp.163-172, 2004.
DOI : 10.1016/j.femsle.2004.08.034

URL : https://hal.archives-ouvertes.fr/pasteur-00753102

E. Moller, G. Bahnweg, H. Sandermann, and H. Geiger, A simple and efficient protocol for isolation of high molecular weight DNA from filamentous fungi, fruit bodies, and infected plant tissues, Nucleic Acids Research, vol.20, issue.22, pp.6115-6121, 1992.
DOI : 10.1093/nar/20.22.6115

J. Sambrook and D. Russell, Molecular cloning: a laboratory manual, 2001.

P. Punt, R. Oliver, M. Dingemanse, P. Pouwels, and C. Van-den-hondel, Transformation of Aspergillus based on the hygromycin B resistance marker from Escherichia coli, Gene, vol.56, issue.1, pp.117-141, 1987.
DOI : 10.1016/0378-1119(87)90164-8

M. Bradford, A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding, Analytical Biochemistry, vol.72, issue.1-2, pp.248-54, 1976.
DOI : 10.1016/0003-2697(76)90527-3

G. Candiano, M. Bruschi, L. Musante, L. Santucci, G. Ghiggeri et al., Blue silver: A very sensitive colloidal Coomassie G-250 staining for proteome analysis, ELECTROPHORESIS, vol.25, issue.9, pp.1327-1360, 2004.
DOI : 10.1002/elps.200305844

J. Romano, G. Nimrod, N. Ben-tal, Y. Shadkchan, K. Baruch et al., Disruption of the Aspergillus fumigatus ECM33 homologue results in rapid conidial germination, antifungal resistance and hypervirulence, Microbiology, vol.152, issue.7, pp.1919-1947, 2006.
DOI : 10.1099/mic.0.28936-0

M. Vodisch, D. Albrecht, F. Lessing, A. Schmidt, R. Winkler et al., Two-dimensional proteome reference maps for the human pathogenic filamentous fungus Aspergillus fumigatus, PROTEOMICS, vol.57, issue.5, pp.1407-1422, 2009.
DOI : 10.1002/pmic.200800394

J. Bruneau, T. Magnin, E. Tagat, R. Legrand, M. Bernard et al., Proteome analysis ofAspergillus fumigatus identifies glycosylphosphatidylinositol-anchored proteins associated to the cell wall biosynthesis, ELECTROPHORESIS, vol.275, issue.13, pp.2812-2835, 2001.
DOI : 10.1002/1522-2683(200108)22:13<2812::AID-ELPS2812>3.0.CO;2-Q

J. Norbeck and A. Blomberg, The level of cAMP-dependent protein kinase A activity strongly affects osmotolerance andosmo-instigated gene expression changes inSaccharomyces cerevisiae, Yeast, vol.11, issue.2, pp.121-158, 2000.
DOI : 10.1002/(SICI)1097-0061(20000130)16:2<121::AID-YEA511>3.0.CO;2-A

W. Zhao, J. Panepinto, J. Fortwendel, L. Fox, B. Oliver et al., Deletion of the Regulatory Subunit of Protein Kinase A in Aspergillus fumigatus Alters Morphology, Sensitivity to Oxidative Damage, and Virulence, Infection and Immunity, vol.74, issue.8, pp.4865-74, 2006.
DOI : 10.1128/IAI.00565-06

C. Godon, G. Lagniel, J. Lee, J. Buhler, S. Kieffer et al., The H2O2 Stimulon in Saccharomyces cerevisiae, Journal of Biological Chemistry, vol.273, issue.35, pp.22480-22489, 1998.
DOI : 10.1074/jbc.273.35.22480

H. Juhnke, B. Krems, P. Kotter, and K. Entian, Mutants that show increased sensitivity to hydrogen peroxide reveal an important role for the pentose phosphate pathway in protection of yeast against oxidative stress, MGG Molecular & General Genetics, vol.56, issue.4, pp.456-64, 1996.
DOI : 10.1007/BF02173011

G. Thorpe, C. Fong, A. N. Higgins, V. Dawes, and I. , Cells have distinct mechanisms to maintain protection against different reactive oxygen species: Oxidative-stress-response genes, Proceedings of the National Academy of Sciences, vol.101, issue.17, pp.6564-6573, 2004.
DOI : 10.1073/pnas.0305888101

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC404085

M. Shimizu, T. Fujii, S. Masuo, K. Fujita, and N. Takaya, Proteomic analysis of Aspergillus nidulans cultured under hypoxic conditions, PROTEOMICS, vol.50, issue.1, pp.7-19, 2009.
DOI : 10.1002/pmic.200701163

U. Bommer and B. Thiele, The translationally controlled tumour protein (TCTP), The International Journal of Biochemistry & Cell Biology, vol.36, issue.3, pp.379-85, 2004.
DOI : 10.1016/S1357-2725(03)00213-9

M. Gnanasekar, G. Dakshinamoorthy, and K. Ramaswamy, Translationally controlled tumor protein is a novel heat shock protein with chaperone-like activity, Biochemical and Biophysical Research Communications, vol.386, issue.2, pp.333-340, 2009.
DOI : 10.1016/j.bbrc.2009.06.028

R. Rid, K. Onder, A. Trost, J. Bauer, H. Hintner et al., H2O2-dependent translocation of TCTP into the nucleus enables its interaction with VDR in human keratinocytes: TCTP as a further module in calcitriol signalling, The Journal of Steroid Biochemistry and Molecular Biology, vol.118, issue.1-2, 2009.
DOI : 10.1016/j.jsbmb.2009.09.015

M. Nagano-ito, A. Banba, and S. Ichikawa, Functional cloning of genes that suppress oxidative stress-induced cell death: TCTP prevents hydrogen peroxide-induced cell death, FEBS Letters, vol.9, issue.8, pp.1363-1370, 2009.
DOI : 10.1016/j.febslet.2009.03.045

M. Reverberi, S. Zjalic, A. Ricelli, F. Punelli, E. Camera et al., Modulation of Antioxidant Defense in Aspergillus parasiticus Is Involved in Aflatoxin Biosynthesis: a Role for the ApyapA Gene, Eukaryotic Cell, vol.7, issue.6, pp.988-1000, 2008.
DOI : 10.1128/EC.00228-07

N. Li, T. Brun, M. Cnop, D. Cunha, D. Eizirik et al., Transient Oxidative Stress Damages Mitochondrial Machinery Inducing Persistent ??-Cell Dysfunction, Journal of Biological Chemistry, vol.284, issue.35, pp.23602-23614, 2009.
DOI : 10.1074/jbc.M109.024323

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2749135

S. Raha and B. Robinson, Mitochondria, oxygen free radicals, disease and ageing, Trends in Biochemical Sciences, vol.25, issue.10, pp.502-510, 2000.
DOI : 10.1016/S0968-0004(00)01674-1

A. Zuin, N. Gabrielli, I. Calvo, S. Garcia-santamarina, K. Hoe et al., Mitochondrial Dysfunction Increases Oxidative Stress and Decreases Chronological Life Span in Fission Yeast, PLoS ONE, vol.280, issue.6, p.2842, 2008.
DOI : 10.1371/journal.pone.0002842.s004

A. Gasch, P. Spellman, C. Kao, O. Eisen, M. Storz et al., Genomic Expression Programs in the Response of Yeast Cells to Environmental Changes, Molecular Biology of the Cell, vol.11, issue.12, pp.4241-57, 2000.
DOI : 10.1091/mbc.11.12.4241

Q. Chen, Q. Ding, J. Thorpe, R. Dohmen, and J. Keller, RNA interference toward UMP1 induces proteasome inhibition in evidence for protein oxidation and autophagic cell death, Free Radical Biology and Medicine, vol.38, issue.2, pp.226-260, 2005.
DOI : 10.1016/j.freeradbiomed.2004.10.019

K. Monastyrskaya, E. Babiychuk, and A. Draeger, The annexins: spatial and temporal coordination of signaling events during cellular stress, Cellular and Molecular Life Sciences, vol.9, issue.3, pp.2623-2665, 2009.
DOI : 10.1007/s00018-009-0027-1

S. Jami, G. Clark, S. Turlapati, C. Handley, S. Roux et al., Ectopic expression of an annexin from Brassica juncea confers tolerance to abiotic and biotic stress treatments in transgenic tobacco, Plant Physiology and Biochemistry, vol.46, issue.12, pp.1019-1049, 2008.
DOI : 10.1016/j.plaphy.2008.07.006

D. Konopka-postupolska, G. Clark, G. Goch, J. Debski, K. Floras et al., The Role of Annexin 1 in Drought Stress in Arabidopsis, PLANT PHYSIOLOGY, vol.150, issue.3, pp.1394-410, 2009.
DOI : 10.1104/pp.109.135228

K. Gorecka, D. Konopka-postupolska, J. Hennig, R. Buchet, and S. Pikula, Peroxidase activity of annexin 1 from Arabidopsis thaliana, Biochemical and Biophysical Research Communications, vol.336, issue.3, pp.868-75, 2005.
DOI : 10.1016/j.bbrc.2005.08.181

J. Mortimer, K. Coxon, A. Laohavisit, and J. Davies, annexin preparation, Plant Signaling & Behavior, vol.30, issue.5, pp.428-458, 2009.
DOI : 10.1016/0005-2728(86)90234-3