Changes in the protein patterns in pea (Pisum sativum L.) roots under the influence of long- and short-term chilling stress and post-stress recovery

Plant Physiology and Biochemistry

Volumn 71, Issue , 2013, Pages 315-324

  Badowiec, Anna ^a   Swigonska, Sylwia ^a   Weidner, Stanisław ^a  

^a UNIVERSITY OF WARMIA AND MAZURY IN OLSZTYN   (Poland)

Author keywords

Chilling stress; Germination; Pea roots; Proteomics; Recovery

Indexed keywords

REACTIVE OXYGEN METABOLITE; STRONTIUM;

2D; ARTICLE; C1, C2; CHILLING STRESS; COLD; CONTROL SAMPLES OF THE SEEDS GERMINATING IN THE OPTIMAL TEMPERATURE; GERMINATION; LONG, CONTINUOUS CHILLING STRESS; LS; LSR; MALDI-TOF MS; MASS SPECTROMETRY; MATRIX-ASSISTED LASED DESORPTION/IONIZATION TIME-OF-FLIGHT MASS SPECTROMETER; METABOLISM; PAGE TWO-DIMENSIONAL ELECTROPHORESIS IN POLYACRYLAMIDE GELS; PEA; PEA ROOTS; PHYSIOLOGY; PLANT ROOT; PROTEOMICS; RECOVERY; RECOVERY AFTER LONG CHILLING STRESS; RECOVERY AFTER SHORT STRESS; ROS; SHORT, RAPID CHILLING STRESS; SS; TWO DIMENSIONAL GEL ELECTROPHORESIS;

2D; C1, C2; CHILLING STRESS; CONTROL SAMPLES OF THE SEEDS GERMINATING IN THE OPTIMAL TEMPERATURE; GERMINATION; LONG, CONTINUOUS CHILLING STRESS; LS; LSR; MALDI-TOF MS; MATRIX-ASSISTED LASED DESORPTION/IONIZATION TIME-OF-FLIGHT MASS SPECTROMETER; PAGE TWO-DIMENSIONAL ELECTROPHORESIS IN POLYACRYLAMIDE GELS; PEA ROOTS; PROTEOMICS; REACTIVE OXYGEN SPECIES; RECOVERY; RECOVERY AFTER LONG CHILLING STRESS; RECOVERY AFTER SHORT STRESS; ROS; SHORT, RAPID CHILLING STRESS; SR; SS;

COLD TEMPERATURE; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; GERMINATION; PEAS; PLANT ROOTS; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION;

EID: 84883807730     PISSN: 09819428     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plaphy.2013.08.001     Document Type: Article

References (40)

1. Allen D.J., Ort D.R. Impact of chilling temperatures on photosynthesis in warm-climate plants. Trends Plant Sci. 2001, 6:36-42.
2. Rymen B., Fiorani F., Kartal F., Vandepoele K., Inz D., Beemster G.T.S. Cold nights impair leaf growth and cell cycle progression in maize through transcriptional changes of cell cycle genes. Plant Physiol. 2007, 143:1429-1438.
3. Kooke R., Keurentjes J.J.B. Multi-dimensional regulation of metabolic networks shaping plant development and performance. J.Exp. Bot. 2012, 63:3321-3323.
4. Rossignol M., Peltier J.B., Mock H.P., Matros A., Maldonado A.M., Jorrin J.V. Plant proteome analysis: a 2004-2006 update. Proteomics 2006, 6:5529-5548.
5. Dumont E., Bahrman N., Goulas E., Valot B., Sellier H., Hilbert J., Vuylsteker C., Lejeune-Henaut I., Delbreil B. Aproteomic approach to decipher chilling response from cold acclimation in pea (Pisum sativum L.). Plant Sci. 2011, 180:86-98.
6. Grimaud F., Renaut J., Dumont E., Sergeant K., Lucau-Danila A., Blervacq A.S., Sellier H., Bahrman N., Lejeune-Hénaut I., Delbreil B., Goulas E. Exploring chloroplastic changes related to chilling and freezing tolerance during cold acclimation of pea (Pisum sativum L.). J.Proteomics 2013, 80:145-159.
7. Pawłowski T.A. Proteome analysis of Norway maple (Acer platanoides L.) seeds dormancy breaking and germination: influence of abscisic and gibberellic acids. BMC Plant Biol. 2009, 9:48.
8. Yan S.P., Zhang Q.Y., Tang Z.C., Su W.A., Sun W.N. Comparative proteomic analysis provides new insights into chilling stress responses in rice. Mol. Cell. Proteomics 2006, 5:484-496.
9. Swigonska S., Weidner S.M. Proteomic analysis of response to long-term continuous stress in roots of germinating soybean seeds. J.Plant Physiol. 2013, 170:470-479.
10. Cui S., Huang F., Wang J., Cheng Y., Liu J. Aproteomic analysis of cold stress responses in rice seedlings. Proteomics 2005, 5:3162-3172.
11. Liu H., Ouyang B., Zhang J., Wang T., Li H. Differential modulation of photosynthesis, signaling, and transcriptional regulation between tolerant and sensitive tomato genotypes under cold stress. PLoS ONE 2012, 7:e50785.
12. Zhou Y., Cai H., Xiao J., Li X., Zhang Q., Lian X. Over-expression of aspartate aminotransferase genes in rice resulted in altered nitrogen metabolism and increased amino acid content in seeds. Theor. Appl. Genet. 2009, 118:1381-1390.
13. Li R., Wang C., Chen T., Chen P. Quantitative proteomic analysis of cold-responsive proteins in Abelmoschus moschatus. J.Anim. Plant Sci. 2012, 14:2006-2023.
14. Hashimoto M., Komatsu S. Proteomic analysis of rice seedlings during cold stress. Proteomics 2007, 7:1293-1302.
15. Abdrakhamanova A., Wang Q.Y., Khokhlova L. Nick PIs microtubule disassembly a trigger for cold acclimation?. Plant Cell Physiol. 2003, 44:676-686.
16. Kocsy G., Galiba G., Brunold C. Role of glutathione in adaptation and signaling during chilling and cold acclimation in plants. Physiol. Plant. 2001, 113:158-164.
17. Liu Y., Shi Y., Song Y., Wang T., Li Y. Characterization of a stress-induced NADP-isocitrate dehydrogenase gene in maize confers salt tolerance in Arabidopsis. J.Plant Biol. 2010, 53:107-112.
18. Frydman J. Folding of newly translated proteins invivo: the role of molecular chaperones. Annu. Rev. Biochem. 2001, 70:603-647.
19. Mathur S., Vyas S., Kapoor S., Tyagi A.K. The mediator complex in plants: structure, phylogeny, and expression profiling of representative genes in a dicot (Arabidopsis) and a monocot (rice) during reproduction and abiotic stress. Plant Physiol. 2011, 157:1609-1627.
20. Moura J.C., Bonine C.A., de Oliveira Fernandes Viana J., Dornelas M.C., Mazzafera P. Abiotic and biotic stresses and changes in the lignin content and composition in plants. J.Integr. Plant Biol. 2010, 52:360-376.
21. Zhou L., Bokhari S.A., Dong C.J., Liu J.Y. Comparative proteomics analysis of the root apoplasts of rice seedlings in response to hydrogen peroxide. PLoS ONE 2011, 6:e16723.
22. Rylott E.L., Gilday A.D., Graham I.A. The Gluconeogenic enzyme phosphoenolpyruvate carboxykinase in Arabidopsis is essential for seedling establishment. Plant Physiol. 2003, 131:1834-1842.
23. Lu W., Tang X., Huo Y., Xu R., Qi S., Huang J., Zheng C., Wu C. Identification and characterization of fructose 1,6-bisphosphate aldolase genes in Arabidopsis reveal a gene family with diverse responses to abiotic stresses. Gene 2012, 503:65-74.
24. Wan X.Y., Liu J.Y. Comparative proteomics analysis reveals an intimate protein network provoked by hydrogen peroxide stress in rice seedling leaves. Mol. Cell. Proteomics 2008, 7:1469-1488.
25. Vashisht A.A., Tuteja N. Stress responsive DEAD-box helicases: a new pathway to engineer plant stress tolerance. J.Photochem. Photobiol. B 2006, 84:150-160.
26. Caruso G., Cavaliere C., Guarino C., Gubbiotti R., Foglia P., Laganà A. Identification of changes in Triticum durum L. leaf proteome in response to salt stress by two-dimensional electrophoresis and MALDI-TOF mass spectrometry. Anal. Bioanal. Chem. 2008, 391:381-390.
27. Brioudes F., Thierry A.M., Chambrier P., Mollereau B., Bendahmane M. Translationally controlled tumor protein is a conserved mitotic growth integrator in animals and plants. Proc. Natl. Acad. Sci. U. S. A. 2010, 14:16384-16389.
28. Yao Y.X., Dong Q.L., Zhai H., You C.X., Hao Y.J. The functions of an apple cytosolic malate dehydrogenase gene in growth and tolerance to cold and salt stresses. Plant Physiol. Biochem. 2011, 49:257-264.
29. Choudhary M.K., Basu D., Datta A., Chakraborty N., Chakraborty S. Dehydration-responsive nuclear proteome of rice (Oryza sativa L.) illustrates protein network, novel regulators of cellular adaptation, and evolutionary perspective. Mol. Cell. Proteomics 2009, 8:1579-1598.
30. Rizhsky L., Liang H., Shuman J., Shulaev V., Davletova S., Mittler R. When defense pathways collide: the response of Arabidopsis to a combination of drought and heat stress. Plant Physiol. 2004, 134:1683-1696.
31. Gamalero E., Glick B.R. Ethylene and abiotic stress tolerance in plants. Environmental Adaptations and Stress Tolerance of Plants in the Era of Climate Change 2012, 395-412. Springer-Verlag. P. Ahmad, M.N.V. Prasad (Eds.).
32. Rösti J., Barton C.J., Albrecht S., Dupree P., Pauly M., Findlay K. UDP-glucose 4-epimerase isoforms UGE2 and UGE4 cooperate in providing UDP-galactose for cell wall biosynthesis and growth of Arabidopsis thaliana. Plant Cell 2007, 19:1565-1579.
33. West G., Inze D., Beemster G.T.S. Cell cycle modulation in the response of the primary root of Arabidopsis to salt stress. Plant Physiol. 2004, 135:1050-1058.
34. Wang W., Vinocur B., Shoseyov O., Altman A. Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response. Trends Plant Sci. 2004, 9:244-252.
35. Dixon D.P., Skipsey M., Edwards R. Roles for glutathione transferases in plant secondary metabolism. Phytochemistry 2010, 71:338-350.
36. Dhugga K.S., Tiwari S.C., Ray P.M. Areversibly glycosylated polypeptide (RGP1) possibly involved in plant cell wall synthesis: purification, gene cloning, and trans-Golgi localization. Proc. Natl. Acad. Sci. U. S. A. 1997, 94:7679-7684.
37. Rodríguez-Serrano M., Romero-Puertas M.C., Pazmiño D.M., Testillano P.S., Risueño M.C., del Río L.A., Sandalio L.M. Cellular response of pea plants to cadmium toxicity: cross talk between reactive oxygen species, nitric oxide, and calcium. Plant Physiol. 2009, 150:229-243.
38. Görg A., Weiss W., Dunn M.J. Current two-dimensional electrophoresis technology for proteomics. Proteomics 2004, 4:3665-3685.
39. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970, 227:680-685.
40. Neuhoff V., Arold N., Taube D., Ehrhardt W. Improved staining of proteins in polyacrylamide gels including isoelectric focusing gels with clear background at nanogram sensitivity using Coomassie Briliant Blue G-250 and R-250. Electrophoresis 1988, 9:255-262.