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Carbohydrate metabolism and cell protection mechanisms differentiate drought tolerance and sensitivity in advanced potato clones (Solanum tuberosum L.)

Bibliographic reference Legay, Sylvain ; Lefèvre, Isabelle S. ; Lamoureux, Didier ; Barreda, Carolina ; Tincopa Luz, Rosalina ; et. al. Carbohydrate metabolism and cell protection mechanisms differentiate drought tolerance and sensitivity in advanced potato clones (Solanum tuberosum L.). In: Functional & Integrative Genomics, Vol. 11, no. 2, p. 275-291 (2011)
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  1. An Soo Hyun, Choi Hyong Woo, Hong Jeum Kyu, Hwang Byung Kook, Regulation and function of the pepper pectin methylesterase inhibitor (CaPMEI1) gene promoter in defense and ethylene and methyl jasmonate signaling in plants, 10.1007/s00425-009-1021-4
  2. Bartels Dorothea, Sunkar Ramanjulu, Drought and Salt Tolerance in Plants, 10.1080/07352680590910410
  3. Cameron K. D., Increased Accumulation of Cuticular Wax and Expression of Lipid Transfer Protein in Response to Periodic Drying Events in Leaves of Tree Tobacco, 10.1104/pp.105.069724
  4. Carvalho André de Oliveira, Gomes Valdirene Moreira, Role of plant lipid transfer proteins in plant cell physiology—A concise review, 10.1016/j.peptides.2007.03.004
  5. Cruz de Carvalho Maria Helena, Drought stress and reactive oxygen species : production, scavenging and signaling, 10.4161/psb.3.3.5536
  6. DEYHOLOS MICHAEL K., Making the most of drought and salinity transcriptomics, 10.1111/j.1365-3040.2009.02092.x
  7. Downing WL, Mauxion F, Fauvarque MO, Reviron MP, de VD, Vartanian N, Giraudat J (1992) A Brassica napus transcript encoding a protein related to the Kunitz protease inhibitor family accumulates upon water stress in leaves, not in seeds. Plant J 2:685–693
  8. Evers D, Bonnechère S, Hoffmann L, Hausman JF (2007) Physiological aspects of abiotic stress of abiotic response in potato. Belg J Bot 140:236–245
  9. Evers Danièle, Lefèvre Isabelle, Legay Sylvain, Lamoureux Didier, Hausman Jean-François, Rosales Raymundo Oscar Gutierrez, Marca Luz Rosalina Tincopa, Hoffmann Lucien, Bonierbale Merideth, Schafleitner Roland, Identification of drought-responsive compounds in potato through a combined transcriptomic and targeted metabolite approach, 10.1093/jxb/erq060
  10. Fernie A. R., Willmitzer L., Molecular and Biochemical Triggers of Potato Tuber Development, 10.1104/pp.010764
  11. Gilmour Sarah J., Fowler Sarah G., Thomashow Michael F., Arabidopsis Transcriptional Activators CBF1, CBF2, and CBF3 have Matching Functional Activities, 10.1023/b:plan.0000040902.06881.d4
  12. Godoy Jos� A., Pardo Jos� M., Pintor-Toro Jos� A., A tomato cDNA inducible by salt stress and abscisic acid: nucleotide sequence and expression pattern, 10.1007/bf00016120
  13. Groppa M. D., Benavides M. P., Polyamines and abiotic stress: recent advances, 10.1007/s00726-007-0501-8
  14. Hanson Andrew D., Nelsen Charles E., Everson Everett H., Evaluation of Free Proline Accumulation as an Index of Drought Resistance Using Two Contrasting Barley Cultivars1, 10.2135/cropsci1977.0011183x001700050012x
  15. Hildmann T., General Roles of Abscisic and Jasmonic Acids in Gene Activation as a Result of Mechanical Wounding, 10.1105/tpc.4.9.1157
  16. Igarashi Yumiko, Yoshiba* Yoshu, Sanada Yukika, Yamaguchi-Shinozaki Kazuko, Wada Keishiro, Shinozaki Kazuo, 10.1023/a:1005702408601
  17. Jackson Stephen D., Multiple Signaling Pathways Control Tuber Induction in Potato, 10.1104/pp.119.1.1
  18. Jongdee B., Fukai S., Cooper M., Leaf water potential and osmotic adjustment as physiological traits to improve drought tolerance in rice, 10.1016/s0378-4290(02)00036-9
  19. Kholová Jana, Hash C. T., Kumar P. Lava, Yadav Rattan S., Kočová Marie, Vadez Vincent, Terminal drought-tolerant pearl millet [Pennisetum glaucum (L.) R. Br.] have high leaf ABA and limit transpiration at high vapour pressure deficit, 10.1093/jxb/erq013
  20. Koizumi Masahiro, Yamaguchi-Shinozaki Kazuko, Tsuji Hideo, Shinozaki Kazuo, Structure and expression of two genes that encode distinct drought-inducible cysteine proteinases in Arabidopsis thaliana, 10.1016/0378-1119(93)90266-6
  21. Krapp Anne, Hofmann Bettina, Schäfer Christian, Stitt Mark, Regulation of the expression ofrbcS and other photosynthetic genes by carbohydrates: a mechanism for the ‘sink regulation’ of photosynthesis?, 10.1111/j.1365-313x.1993.00817.x
  22. Lea P.J., Sodek L., Parry M.A.J., Shewry P.R., Halford N.G., Asparagine in plants, 10.1111/j.1744-7348.2006.00104.x
  23. Legay Sylvain, Lamoureux Didier, Hausman Jean-François, Hoffmann Lucien, Evers Danièle, Monitoring gene expression of potato under salinity using cDNA microarrays, 10.1007/s00299-009-0780-5
  24. Ma Yuan-yuan, Song Wei-yi, Liu Zi-hui, Zhang Hong-mei, Guo Xiu-lin, Shao Hong-bo, Ni Fu-tai, The dynamic changing of Ca2+ cellular localization in maize leaflets under drought stress, 10.1016/j.crvi.2008.12.003
  25. Mane Shrinivasrao P., Robinet Cecilia Vasquez, Ulanov Alexander, Schafleitner Roland, Tincopa Luz, Gaudin Amelie, Nomberto Giannina, Alvarado Carlos, Solis Christian, Bolivar Luis Avila, Blas Raul, Ortega Oscar, Solis Julio, Panta Ana, Rivera Cristina, Samolski Ilanit, Carbajulca Doris H., Bonierbale Meredith, Pati Amrita, Heath Lenwood S., Bohnert Hans J., Grene Ruth, Molecular and physiological adaptation to prolonged drought stress in the leaves of two Andean potato genotypes, 10.1071/fp07293
  26. Miller Gad, Shulaev Vladimir, Mittler Ron, Reactive oxygen signaling and abiotic stress, 10.1111/j.1399-3054.2008.01090.x
  27. Nicot N., Housekeeping gene selection for real-time RT-PCR normalization in potato during biotic and abiotic stress, 10.1093/jxb/eri285
  28. Nishizawa A., Yabuta Y., Shigeoka S., Galactinol and Raffinose Constitute a Novel Function to Protect Plants from Oxidative Damage, 10.1104/pp.108.122465
  29. Oufir Mouhssin, Legay Sylvain, Nicot Nathalie, Van Moer Kris, Hoffmann Lucien, Renaut Jenny, Hausman Jean-François, Evers Danièle, Gene expression in potato during cold exposure: Changes in carbohydrate and polyamine metabolisms, 10.1016/j.plantsci.2008.08.010
  30. Paul M. J., Pellny T. K., Carbon metabolite feedback regulation of leaf photosynthesis and development, 10.1093/jxb/erg052
  31. Pelloux J., Jolivet Y., Fontaine V., Banvoy J., Dizengremel P., Changes in Rubisco and Rubisco activase gene expression and polypeptide content inPinus halepensisM. subjected to ozone and drought, 10.1046/j.1365-3040.2001.00665.x
  32. Plant AL, Bray EA (1999) Regulation of gene expression by abscisic acid during environmental stress. In: Lerner HR (ed) Plant responses to environmental stresses: from phytohormones to genome reorganization. Mark Dekker, New York, pp 303–331
  33. Rabbani M. A., Monitoring Expression Profiles of Rice Genes under Cold, Drought, and High-Salinity Stresses and Abscisic Acid Application Using cDNA Microarray and RNA Gel-Blot Analyses, 10.1104/pp.103.025742
  34. Rorat Tadeusz, Plant dehydrins — Tissue location, structure and function, 10.2478/s11658-006-0044-0
  35. Schafleitner Roland, Gaudin Amélie, Gutierrez Rosales Raymundo Oscar, Alvarado Aliaga Carlos Alberto, Bonierbale Merideth, Proline accumulation and real time PCR expression analysis of genes encoding enzymes of proline metabolism in relation to drought tolerance in Andean potato, 10.1007/s11738-006-0003-4
  36. Schafleitner Roland, Gutierrez Rosales Raymundo Oscar, Gaudin Amelie, Alvarado Aliaga Carlos Alberto, Martinez Giannina Nomberto, Tincopa Marca Luz Rosalina, Bolivar Luis Avila, Delgado Felipe Mendiburu, Simon Reinhard, Bonierbale Merideth, Capturing candidate drought tolerance traits in two native Andean potato clones by transcription profiling of field grown plants under water stress, 10.1016/j.plaphy.2007.06.003
  37. Shi Lan-Xin, Lorković Zdravko J., Oelmüller Ralf, Schröder Wolfgang P., The Low Molecular Mass PsbW Protein Is Involved in the Stabilization of the Dimeric Photosystem II Complex inArabidopsis thaliana, 10.1074/jbc.m006300200
  38. Shinozaki Kazuo, Yamaguchi-Shinozaki Kazuko, Seki Motoaki, Regulatory network of gene expression in the drought and cold stress responses, 10.1016/s1369-5266(03)00092-x
  39. Sundaresan S., Sudhakaran P. R., Water stress-induced alterations in the proline metabolism of drought-susceptible and -tolerant cassava (Manihot esculenta) cultivars, 10.1111/j.1399-3054.1995.tb00978.x
  40. Taji Teruaki, Ohsumi Chieko, Iuchi Satoshi, Seki Motoaki, Kasuga Mie, Kobayashi Masatomo, Yamaguchi-Shinozaki Kazuko, Shinozaki Kazuo, Important roles of drought- and cold-inducible genes for galactinol synthase in stress tolerance in Arabidopsis thaliana, 10.1046/j.0960-7412.2001.01227.x
  41. Treviño Marcela B., Connell Mary A. O', Three Drought-Responsive Members of the Nonspecific Lipid-Transfer Protein Gene Family inLycopersicon pennelliiShow Different Developmental Patterns of Expression, 10.1104/pp.116.4.1461
  42. Valliyodan Babu, Nguyen Henry T, Understanding regulatory networks and engineering for enhanced drought tolerance in plants, 10.1016/j.pbi.2006.01.019
  43. van Bel Aart J. E., Hess Paul H., Hexoses as phloem transport sugars: the end of a dogma?, 10.1093/jxb/erm294
  44. Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, De Paepe A, Speleman F (2002) Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol 3: research 0034.1–0034.11
  45. Vasquez-Robinet Cecilia, Mane Shrinivasrao P., Ulanov Alexander V., Watkinson Jonathan I., Stromberg Verlyn K., De Koeyer David, Schafleitner Roland, Willmot David B., Bonierbale Merideth, Bohnert Hans J., Grene Ruth, Physiological and molecular adaptations to drought in Andean potato genotypes, 10.1093/jxb/ern073
  46. Vieira Dos Santos Christina, Rey Pascal, Plant thioredoxins are key actors in the oxidative stress response, 10.1016/j.tplants.2006.05.005
  47. Vierstra R D, Protein Degradation in Plants, 10.1146/annurev.pp.44.060193.002125
  48. Waters Elizabeth R., Aevermann Brian D., Sanders-Reed Zipporah, Comparative analysis of the small heat shock proteins in three angiosperm genomes identifies new subfamilies and reveals diverse evolutionary patterns, 10.1007/s12192-008-0023-7
  49. Watkinson Jonathan I., Hendricks Lori, Sioson Allan A., Vasquez-Robinet Cecilia, Stromberg Verlyn, Heath Lenwood S., Schuler Mary, Bohnert Hans J., Bonierbale Merideth, Grene Ruth, Accessions of Solanum tuberosum ssp. andigena show differences in photosynthetic recovery after drought stress as reflected in gene expression profiles, 10.1016/j.plantsci.2006.07.010
  50. Wolfinger RD, Chang M (1998) Comparing the SAS GLM and MIXED procedures for repeated measures. In SUGI Proceedings, Cary, NC, USA
  51. Xie Q., Arabidopsis NAC1 transduces auxin signal downstream of TIR1 to promote lateral root development, 10.1101/gad.852200
  52. Xue Gang-Ping, McIntyre C. Lynne, Glassop Donna, Shorter Ray, Use of expression analysis to dissect alterations in carbohydrate metabolism in wheat leaves during drought stress, 10.1007/s11103-008-9311-y
  53. Zhang Chun-sheng, Lu Qin, Verma Desh Pal S., Removal of Feedback Inhibition of Δ1-Pyrroline-5-carboxylate Synthetase, a Bifunctional Enzyme Catalyzing the First Two Steps of Proline Biosynthesis in Plants, 10.1074/jbc.270.35.20491
  54. Zhou Junli, Wang Xiangfeng, Jiao Yuling, Qin Yonghua, Liu Xigang, He Kun, Chen Chen, Ma Ligeng, Wang Jian, Xiong Lizhong, Zhang Qifa, Fan Liumin, Deng Xing Wang, Global genome expression analysis of rice in response to drought and high-salinity stresses in shoot, flag leaf, and panicle, 10.1007/s11103-006-9111-1