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Comparative proteomic analysis of seedling leaves of different salt tolerant soybean genotypes
Authors:Ma Hongyu  Song Liru  Shu Yingjie  Wang Shuang  Niu Juan  Wang Zhankui  Yu Tian  Gu Weihong  Ma Hao
Affiliation:
  • a State Key Laboratory of Crop Genetics and Germplasm Enhancement, National Center for Soybean Improvement, Nanjing Agricultural University, Nanjing, Jiangsu Province 210095, PR China
  • b Animal and Plant Introduction and Research Center, Shanghai Agricultural Academy, Shanghai 201106, PR China
  • Abstract:Salinity is one of the major environmental constraints limiting yield of crop plants in many semi-arid and arid regions around the world. To understand responses in soybean seedling to salt stress at proteomic level, the extracted proteins from seedling leaves of salt-sensitive genotype Jackson and salt-tolerant genotype Lee 68 under 150 mM NaCl stress for 1, 12, 72 and 144 h, respectively, were analyzed by 2-DE. Approximately 800 protein spots were detected on 2-DE gels. Among them, 91 were found to be differently expressed, with 78 being successfully identified by MALDI-TOF-TOF. The identified proteins were involved in 14 metabolic pathways and cellular processes. Based on most of the 78 salt-responsive proteins, a salt stress-responsive protein network was proposed. This network consisted of several functional components, including balancing between ROS production and scavenging, accelerated proteolysis and reduced biosynthesis of proteins, impaired photosynthesis, abundant energy supply and enhanced biosynthesis of ethylene. Salt-tolerant genotype Lee 68 possessed the ability of higher ROS scavenging, more abundant energy supply and ethylene production, and stronger photosynthesis than salt-sensitive genotype Jackson under salt stress, which may be the major reasons why it is more salt-tolerant than Jackson.
    Keywords:AAS, aspartate aminotransferase   ACO, 1-aminocyclopropane-1-carboxylate oxidase   ACC, 1-aminocyclopropane-1-carboxylate   ACS, 1-aminocyclopropane-1-carboxylate synthetase   Ald, aldolase   APX, ascorbate peroxidase   ASD, aspartate-semialdehyde dehydrogenase   ATP, adenosine-triphosphate   BIP, 2,3-biphosphoglycerate-independent phosphoglycerate mutase, putative   CAT, catalase   CMD, cytosolic malate dehydrogenase   DFR, dihydroflavonol reductase   EF2, elongation factor 2   EF-G, translation elongation factor EF-G   G3PD, glyceraldehyde 3-phosphate dehydrogenase   Glyox, putative glyoxalase   GRP, glycine-rich RNA-binding protein   HPD, homologous to plastidic aldolase   KEGG, kyoto encyclopedia of genes and genomes   NCBI, national center for biotechnology information   OEEP2, oxygen-evolving enhancer protein 2, chloroplastic   OX, oxidation   PB, protein biosynthesis   PDH, pyruvate dehydrogenase   PDI, protein disulfide isomerase-like   Perox, peroxiredoxin   POD, peroxidase   PP, proteolytic proteins   PS I, photosystem I   PS II, photosystem II   RBPs, RNA-binding proteins   RED, reduction   RLS, ribulose 1,5-bisphosphate carboxylase large subunit   RV, relative volume   SAMS, S-adenosylmethionine synthetase   SOD, superoxide dismutase   TatBP, rice homologue of Tat binding protein   TCA cycle, tricarboxylic acid cycle   TCTP, translationally-controlled tumor protein   Trans, transketolase.
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