Structural and functional characterization of annexin 1 from Medicago truncatula

Plant Physiology and Biochemistry

Volumn 73, Issue , 2013, Pages 56-62

  Kodavali, Praveen Kumar ^a   Skowronek, Krzysztof ^a   Koszela Piotrowska, Izabela ^a   Strzelecka Kiliszek, Agnieszka ^a   Pawlowski, Krzysztof ^a,b   Pikula, Slawomir ^a  

^a NENCKI INSTITUTE OF EXPERIMENTAL BIOLOGY   (Poland)

^b WARSAW UNIVERSITY OF LIFE SCIENCES   (Poland)

Author keywords

Annexin 1; Ion channel; Medicago truncatula; Protein structure

Indexed keywords

ANNEXIN; CATION; ION CHANNEL; RECOMBINANT PROTEIN; VEGETABLE PROTEIN;

3-D; ANNAT1-ANNAT8; ANNEXIN 1; ANNEXINS 1-8 FROM ARABIDOPSIS THALIANA; ANNEXINS 1-9 FROM MEDICAGO TRUNCATULA; ANNMT1-ANNMT9; ANXA1-A11 AND ANXA13; ARTICLE; BARREL MEDIC; BIOLOGICAL MODEL; CELL MEMBRANE PERMEABILITY; CHEMICAL STRUCTURE; CHEMISTRY; COLUMN VOLUMES; CVS; MAMMALIAN ANNEXINS A1-A11 AND A13; METABOLISM; MICROBIOLOGY; MYCORRHIZA; NODULATION; PHENYL METHYL SULFONYL FLUORIDE; PMSF; PROTEIN CONFORMATION; PROTEIN STRUCTURE; SIGNAL TRANSDUCTION; THREE-DIMENSIONAL;

3-D; ANNAT1-ANNAT8; ANNEXIN 1; ANNEXINS 1-8 FROM ARABIDOPSIS THALIANA; ANNEXINS 1-9 FROM MEDICAGO TRUNCATULA; ANNMT1-ANNMT9; ANXA1-A11 AND ANXA13; COLUMN VOLUMES; CVS; ION CHANNEL; MAMMALIAN ANNEXINS A1-A11 AND A13; MEDICAGO TRUNCATULA; PHENYL METHYL SULFONYL FLUORIDE; PMSF; PROTEIN STRUCTURE; THREE-DIMENSIONAL;

ANNEXINS; CATIONS; CELL MEMBRANE PERMEABILITY; ION CHANNELS; MEDICAGO TRUNCATULA; MODELS, BIOLOGICAL; MOLECULAR STRUCTURE; MYCORRHIZAE; PLANT PROTEINS; PLANT ROOT NODULATION; PROTEIN CONFORMATION; RECOMBINANT PROTEINS; SIGNAL TRANSDUCTION;

EID: 84884302683     PISSN: 09819428     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plaphy.2013.08.010     Document Type: Article

References (50)

1. Gerke V., Moss S.E. Annexins: from structure to function. Physiol. Rev. 2002, 82:331-371.
2. Mortimer J.C., Laohavisit A., Macpherson N., Webb A., Brownlee C., Battey N.H., Davies J.M. Annexins: multifunctional components of growth and adaptation. J.Exp. Bot. 2008, 59:533-544.
3. Clark G.B., Morgan R.O., Fernandez M.-P., Roux S.J. Evolutionary adaptation of plant annexins has diversified their molecular structures, interactions and functional roles. New Phytol. 2012, 196:695-712.
4. Konopka-Postupolska D., Clark G., Hofmann A. Structure, function and membrane interactions of plant annexins: an update. Plant Sci. 2011, 181:230-241.
5. Hofmann A., Proust J., Dorowski A., Schantz R., Huber R. Annexin 24 from Capsicum annuum. X-ray structure and biochemical characterization. J.Biol. Chem. 2000, 275:8072-8082.
6. 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.
7. Gorecka K.M., Thouverey C., Buchet R., Pikula S. Potential role of annexin AnnAt1 from Arabidopsis thaliana in pH-mediated cellular response to environmental stimuli. Plant Cell Physiol. 2007, 48:792-803.
8. Chandran D., Sharopova N., Ivashuta S., Gantt J.S., Vandenbosch K.A., Samac D.A. Transcriptome profiling identified novel genes associated with aluminum toxicity, resistance and tolerance in Medicago truncatula. Planta 2008, 228:151-166.
9. Konopka-Postupolska D., Clark G., Goch G., Debski J., Floras K., Cantero A., Fijolek B., Roux S., Hennig J. The role of annexin 1 in drought stress in Arabidopsis. Plant Physiol. 2009, 150:1394-1410.
10. 2+-permeable conductance. Plant Cell 2009, 21:479-493.
11. 2+-permeable conductance. Plant Signal. Behav. 2009, 4:989-991.
12. Huh S.M., Noh E.K., Kim H.G., Jeon B.W., Bae K., Hu H.C., Kwak J.M., Park O.K. Arabidopsis annexins AnnAt1 and AnnAt4 interact with each other and regulate drought and salt stress responses. Plant Cell Physiol. 2010, 51:1499-1514.
13. Cantero A., Barthakur S., Bushart T.J., Chou S., Morgan R.O., Fernandez M.P., Clark G.B., Roux S.J. Expression profiling of the Arabidopsis annexin gene family during germination, de-etiolation and abiotic stress. Plant Physiol. Biochem. 2000, 44:13-24.
14. Clark G.B., Sessions A., Eastburn D.J., Roux S.J. Differential expression of members of the annexin multigene family in Arabidopsis. Plant Physiol. 2001, 126:1072-1084.
15. Okamoto T., Higuchi K., Shinkawa T., Isobe T., Lörz H., Koshiba T., Kranz E. Identification of major proteins in maize egg cells. Plant Cell Physiol. 2004, 45:1406-1412.
16. Yang Y.W., Bian S.M., Yao Y., Liu J.Y. Comparative proteomic analysis provides new insights into the fiber elongating process in cotton. J.Proteome Res. 2008, 7:4623-4637.
17. 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.
18. Thonat C., Mathieu C., Crevecoeur M., Penel C., Gaspar T., Boyer N. Effects of a mechanical stimulation of localization of annexin-like proteins in Bryonia dioica internodes. Plant Physiol. 1997, 114:981-988.
19. Kovács I., Ayaydin F., Oberschall A., Ipacs I., Bottka S., Pongor S., Dudits D., Tóth E.C. Immunolocalization of a novel annexin-like protein encoded by a stress and abscisic acid responsive gene in alfalfa. Plant J. 1998, 15:185-197.
20. Breton G., Vazquez-Tello A., Danyluk J., Sarhan F. Two novel intrinsic annexins accumulate in wheat membranes in response to low temperature. Plant Cell Physiol. 2000, 41:177-184.
21. Jami S.K., Dalal A., Divya K., Kirti P.B. Molecular cloning and characterization of five annexin genes from Indian mustard (Brassica juncea L. Czern and Coss). Plant Physiol. Biochem. 2009, 47:977-990.
22. Hofmann A., Benz J., Liemann S., Huber R. Voltage dependent binding of annexin V, annexin VI and annexin VII-core to acidic phospholipid membranes. Biochim. Biophys. Acta 1997, 1330:254-264.
23. Golczak M., Kicinska A., Bandorowicz-Pikula J., Buchet R., Szewczyk A., Pikula S. Acidic pH-induced folding of annexin VI is a prerequisite for its insertion into lipid bilayers and formation of ion channels by the protein molecules. FASEB J. 2001, 15:1083-1085.
24. De Carvalho-Niebel F., Lescure N., Cullimore J.V., Gamas P. The Medicago truncatula MtAnn1 gene encoding an annexin is induced by Nod factors and during the symbiotic interaction with Rhizobium meliloti. Mol. Plant Microbe Interact. 1998, 11:504-513.
25. De Carvalho-Niebel F., Timmers A.C., Chabaud M., Defaux-Petras A., Barker D.G. The Nod factor-elicited annexin MtAnn1 is preferentially localized at the nuclear periphery in symbiotically activated root tissues of Medicago truncatula. Plant J. 2002, 32:343-352.
26. Young N.D., Debellé F., Oldroyd G.E., et al. The Medicago genome provides insight into the evolution of rhizobial symbioses. Nature 2011, 480:520-524.
27. Manthey K., Krajinski F., Hohnjec N., Firnhaber C., Pühler A., Perlick A.M., Küster H. Transcriptome profiling in root nodules and arbuscular mycorrhiza identifies a collection of novel genes induced during Medicago truncatula root endosymbioses. Mol. Plant Microbe Interact. 2004, 17:1063-1077.
28. Moss S.E., Morgan R.O. The annexins. Genome Biol. 2004, 5:219.
29. 2+-permeable conductance. Plant Cell 2009, 21:479-493.
30. Dabitz N., Hu N.J., Yusof A.M., Tranter N., Winter A., Daley M., Zschörnig O., Brisson A., Hofmann A. Structural determinants for plant annexin-membrane interactions. Biochemistry 2005, 44:16292-16300.
31. Simões I., Mueller E.C., Otto A., Bur D., Cheung A.Y., Faro C., Pires E. Molecular analysis of the interaction between cardosin A and phospholipase Dα. Identification of RGD/KGE sequences as binding motifs for C2 domains. FEBS J. 2005, 272:5786-5798.
32. Laval V., Chabannes M., Carrière M., Canut H., Barre A., Rougé P., Pont-Lezica R., Galaud J. Afamily of Arabidopsis plasma membrane receptors presenting animal beta-integrin domains. Biochim. Biophys. Acta 1999, 1435:61-70.
33. Labouré A.M., Faik A., Mandaron P., Falconet D. RGD-dependent growth of maize calluses and immunodetection of an integrin-like protein. FEBS Lett. 1999, 442:123-128.
34. Knepper C., Savory E.A., Day B. Arabidopsis NDR1 is an integrin-like protein with a role in fluid loss and plasma membrane-cell wall adhesion. Plant Physiol. 2011, 156:286-300.
35. Hofmann A., Delmer D.P., Wlodawer A. The crystal structure of annexin Gh1 from Gossypium hirsutum reveals an unusual S3 cluster. Eur. J. Biochem. 2003, 270:2557-2564.
36. Hu N.J., Yusof A.M., Winter A., Osman A., Reeve A.K., Hofmann A. The crystal structure of calcium-bound annexin Gh1 from Gossypium hirsutum and its implications for membrane binding mechanisms of plant annexins. J.Biol. Chem. 2008, 283:18314-18322.
37. 2+ sensors in plant signaling. Biochem. J. 2009, 425:27-40.
38. Kastl K., Menke M., Lüthgens E., Faiss S., Gerke V., Janshoff A., Steinem C. Partially reversible adsorption of annexin A1 on POPC/POPS bilayers investigated by QCM measurements, SFM, and DMC simulations. ChemBioChem 2006, 7:106-115.
39. Langen R., Isas J.M., Luecke H., Haigler H.T., Hubbell W.L. Membrane-mediated assembly of annexins studied by site-directed spin labeling. J.Biol. Chem. 1998, 273:22453-22457.
40. Kim Y.E., Isas J.M., Haigler H.T., Langen R. Ahelical hairpin region of soluble annexin B12 refolds and forms a continuous transmembrane helix at mildly acidic pH. J.Biol. Chem. 2005, 280:32398-32404.
41. Amor B.B., Shaw S.L., Oldroyd G.E., Maillet F., Penmetsa R.V., Cook D., Long S.R., Dénarié J., Gough C. The NFP locus of Medicago truncatula controls an early step of Nod factor signal transduction upstream of a rapid calcium flux and root hair deformation. Plant J. 2003, 34:495-506.
42. Madsen E.B., Madsen L.H., Radutoiu S., Olbryt M., Rakwalska M., Szczyglowski K., Sato S., Kaneko T., Tabata S., Sandal N., Stougaard J. Areceptor kinase gene of the LysM type is involved in legume perception of rhizobial signals. Nature 2003, 425:637-640.
43. Kurkdjian A., Bouteau F., Pennarun A.M., Convert M., Cornel D., Rona J.P., Bousquet U. Ion currents involved in early Nod factor response in Medicago sativa root hairs: a discontinuous single-electrode voltage-clamp study. Plant J. 2000, 22:9-17.
44. Shaw S.L., Long S.R. Nod factor elicits two separable calcium responses in Medicago truncatula root hair cells. Plant Physiol. 2003, 131:976-984.
45. Miwa H., Sun J., Oldroyd G.E., Downie J.A. Analysis of calcium spiking using a cameleon calcium sensor reveals that nodulation gene expression is regulated by calcium spike number and the developmental status of the cell. Plant J. 2006, 48:883-894.
46. Dereeper A., Guignon V., Blanc G., Audic S., Buffet S., Chevenet F., Dufayard J.F., Guindon S., Lefort V., Lescot M., Claverie J.M., Gascuel O. Phylogeny.fr: robust phylogenetic analysis for the non-specialist. Nucleic Acids Res. 2008, 36:W465-W469.
47. Pawlowski M., Gajda M.J., Matlak R., Bujnicki J.M. MetaMQAP: a meta-server for the quality assessment of protein models. BMC Bioinform. 2008, 9:403.
48. Reeves J.P., Dowben R.M. Formation and properties of thin-walled phospholipid vesicles. J.Cell. Physiol. 1969, 73:41-60.
49. 2+ regulates mitochondrial ATP-dependent potassium channel from heart. FEBS Lett. 2005, 579:1625-1632.
50. Hille B. Selective permeability: independence. Ion Channels of Excitable Membranes 2001, 441-470. Sinauer Associates Inc., Sunderland, MA. third ed.