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http://dx.doi.org/10.7235/hort.2012.11122

Analyses of Inter-cultivar Variation for Salinity Tolerance in Six Korean Rapeseed Cultivars  

Lee, Yong-Hwa (Bioenergy Crop Research Center, National Institute of Crop Science, Rural Development Administration)
Lee, Tae-Sung (Bioenergy Crop Research Center, National Institute of Crop Science, Rural Development Administration)
Kim, Kwang-Soo (Bioenergy Crop Research Center, National Institute of Crop Science, Rural Development Administration)
Jang, Young-Seok (Bioenergy Crop Research Center, National Institute of Crop Science, Rural Development Administration)
Nam, Sang-Sik (Planning & Coordination Division, National Institute of Crop Science, Rural Development Administration)
Park, Kwang-Geun (Bioenergy Crop Research Center, National Institute of Crop Science, Rural Development Administration)
Publication Information
Horticultural Science & Technology / v.30, no.4, 2012 , pp. 417-425 More about this Journal
Abstract
Salinity stress is one of the most serious factors limiting the productivity of agricultural crops. The aim of this study was to assess inter-cultivar (intraspecific) variation for salinity tolerance in six Korean rapeseed (Brassica napus L.) cultivars at the seedling stage. The effect of three different salinity stress levels (EC 4, 8, and 16 $dS{\cdot}m^{-1}$) on seedlings of six cultivars was investigated through leaf size, leaf dry weight, and leaf chlorosis. At the highest salinity level (16 $dS{\cdot}m^{-1}$), the mean decrease of leaf dry weight in 'Sunmang', 'Tammi', 'Tamla', 'Naehan', 'Youngsan', and 'Halla' was about 56.2, 56.9, 78.4, 79.3, 77.4, and 80.9%, respectively. 'Tammi' and 'Sunmang' showed much less reduction in leaf dry weight than all the other cultivars. In addition, diluted seawater treatments increased the occurrence of leaf chlorosis in six cultivars. At EC 8 and 16 $dS{\cdot}m^{-1}$, 'Naehan', 'Youngsan', and 'Halla' showed a higher level of leaf chlorosis than 'Tammi' 'Sunmang', and 'Tamla'. On the basis of these results, six cultivars were placed into salinity-tolerant and sensitive groups. 'Tammi' and 'Sunmang' were the salinity-tolerant cultivars, while 'Naehan', 'Halla', 'Youngsan', and 'Tamla' were the salinity-sensitive cultivars. 'Tammi' and 'Naehan' rated as the most tolerant and most sensitive cultivar, respectively. To further analyze protein expression profiles in 'Tammi' and 'Naehan', 2-D proteomic analysis was performed using the plants grown under diluted seawater treatments. We identified eight differentially displayed proteins that participate in photosynthesis, carbon assimilation, starch and sucrose metabolism, amino acid metabolism, cold and oxidative stress, and calcium signaling. The differential protein expressions in 'Tammi' and 'Naehan' are likely to correlate with the differential growth responses of both cultivars to salinity stress. These data suggest that 'Tammi' is better adapted to salinity stressed environments than 'Naehan'.
Keywords
Brassica; seawater;
Citations & Related Records
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1 Tuteja, N. 2007. Mechanisms of high salinity tolerance in plants. Methods Enzymol. 428:410-438.
2 Uno, Y., M.A. Rodriguez Milla, E. Maher, and J.C. Cushman. 2009. Identification of proteins that interact with catalytically active calcium-dependent protein kinases from Arabidopsis. Mol. Genet. Genomics 281:375-390.   DOI
3 Vera-Estrella, R., B.J. Barkla, L. García-Ramírez, and O. Pantoja. 2005. Salt Stress in Thellungiella halophila Activates $Na^{+}$ Transport Mechanisms Required for Salinity Tolerance. Physiol. Plant. 139:1507-1517.   DOI
4 Xu, K., P. Hong, and L.J. Luo. 2009. Overexpression of AtNHX1, a vacuolar $Na^{+}/H^{+}$ antiporter from Arabidopsis thalina, in Petunia hybrida, enhances salt and drought tolerance. J. Plant Biol. 52:453-461.   DOI
5 Yamaguchi-Shinozaki, K. and K. Shinozaki. 2006. Transcriptional regulatory networks in cellular responses and tolerance to dehydration and cold stresses. Annu. Rev. Plant Biol. 57:781-803.   DOI
6 Zhang, H.X. and E. Blumwald. 2001. Transgenic salt-tolerant tomato plants accumulate salt in foliage but not in fruit. Nat. Biotechnol. 19:765-768.   DOI   ScienceOn
7 Zhang, H.X., J.N. Hodson, J.P. Williams, and E. Blumwald. 2001. Engineering salt-tolerant Brassica plants: Characterization of yield and seed oil quality in transgenic plants with increased vacuolar sodium accumulation. Proc. Natl. Acad. Sci. USA 98:12832-12836.   DOI   ScienceOn
8 Gaxiola, R.A., R. Rao, A. Sherman, P. Grisafi, S.L. Alper, and G.R. Fink. 1999. The Arabidopsis thaliana proton transporters, AtNhx1 and Avp1, can function in cation detoxification in yeast. Proc. Natl. Acad. Sci. USA 96:1480-1485.   DOI   ScienceOn
9 Gosti, F., Bertauche, N., Vartanian, N. and J. Giraudat. 1995. Abscisic acid-dependent and -independent regulation of gene expression by progressive drought in Arabidopsis thaliana. Mol. Gen. Genet. 246:10-18.   DOI
10 Goulas, E., M. Schubert, T. Kieselbach, L.A. Kleczkowski, P. Gardeström, W. Schröder, and V. Hurry. 2006. The chloroplast lumen and stromal proteomes of Arabidopsis thaliana show differential sensitivity to short- and long-term exposure to low temperature. Plant J. 47:720-734.   DOI
11 He, T. and G.R. Cramer. 1992. Growth and mineral nutrition of six rapid-cycling Brassica species in response to seawater salinity. Plant Soil 139:285-294.   DOI
12 Khan, M.A. and S. Gulzar. 2003. Germination responses of Sporobolus ioclados: A saline desert grass. J. Arid Environ. 55:453-464.   DOI
13 Lunn, J.E., A.R. Ashton, M.D. Hatch, and H.W. Heldt. 2000. Purification, molecular cloning, and sequence analysis of sucrose-6F-phosphate phosphohydrolase from plants. Proc. Natl. Acad. Sci. USA. 97:12914-12919.   DOI
14 Nambara, E. and A. Marion-Poll. 2005. Abscisic acid biosynthesis and catabolism. Annu. Rev. Plant Biol. 56:165-185.   DOI
15 Paludan-Müller, G., H. Saxe, L.B. Pedersen, and T.B. Randrup. 2002. Differences in salt sensitivity of four deciduous tree species to soil or airborne salt. Physiol. Plant. 114:223-230.   DOI
16 Shevchenko, A., M. Wilm, O. Vorm, and M. Mann. 1996. Mass spectrometric sequencing of proteins silver-stained polyacrylamide gels. Anal. Chem. 68:850-858.   DOI   ScienceOn
17 Abdel-Hady, M.S. 2001. Wheat plantlets production via shoot tips under salinity stress. J. Agric. Sci. 26:4841-4857.
18 Anderson, N.L., R. Esquer-Blasco, J.P. Hofmann, and N.G. Anderson. 1991. A two-dimensional gel database of rat liver proteins useful in gene regulation and drug effects studies. Electrophoresis 12:907-930.   DOI
19 Abu-Romman, S. and M. Shatnawi. 2010. Isolation and expression analysis of chloroplastic copper/zinc superoxide dismutase gene in barley. South African J. Bot. 77:328-334.
20 Albassam, B.A. 2001. Effect of nitrate nutrition on growth and nitrogen assimilation of pearl millet exposed to sodium chloride stress. J. Plant Nutr. 24:1325-1335.   DOI
21 Apse, M.P., G.S. Aharon, W.A. Snedden, and E. Blumwald. 1999. Salt tolerance conferred by overexpression of a vacuolar $Na^{+}/H^{+}$ antiport in Arabidopsis. Science 285:1256-1258.   DOI   ScienceOn
22 Ashraf, M. and T. McNeilly. 2004. Salinity Tolerance in Brassica Oilseeds. Crit. Rev. Plant Sci. 23:157-174.   DOI
23 Bradford, M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72:248-254.   DOI   ScienceOn
24 Bybordi, A. and J. Tabatabaei. 2009. Effect of Salinity Stress on Germination and Seedling Properties in Canola Cultivars (Brassica napus L.). Not. Bot. Hort. Agrobot. Cluj 37:71-76.
25 Engel, N., K. van den Daele, U. Kolukisaoqlu, K. Morgenthal, W. Weckwerth, T. Pärnik, O. Keerberg, and H. Bauwe. 2007. Deletion of glycine decarboxylase in Arabidopsis is lethal under nonphotorespiratory conditions. Plant Physiol. 144: 1328-1335.   DOI