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Differences in leaf proteome response to cold acclimation between Lolium perenne plants with distinct levels of frost tolerance
Authors:Bocian Aleksandra  Kosmala Arkadiusz  Rapacz Marcin  Jurczyk Barbara  Marczak Łukasz  Zwierzykowski Zbigniew
Institution:a Institute of Plant Genetics, Polish Academy of Sciences, Strzeszyńska 34, 60-479 Poznań, Poland
b University of Agriculture in Kraków, Department of Plant Physiology, Pod?u?na 3, 30-239 Cracow, Poland
c Institute of Bioorganic Chemistry, Polish Academy of Sciences, Noskowskiego 12/14, 61-704 Poznań, Poland
Abstract:Perennial ryegrass (Lolium perenne) is a high quality forage and turf grass mainly due to its excellent nutritive values and rapid establishment rate. However, this species has limited ability to perform in harsh winter climates. Though winter hardiness is a complex trait, it is commonly agreed that frost tolerance (FT) is its main component. Species growing in temperate regions can acquire FT through exposure to low, non-lethal temperatures, a phenomenon known as cold acclimation (CA). The research on molecular basis of FT has been performed on the model plants, but they are not well adapted to extreme winter climates. Thus, the mechanisms of cell response to low temperature in winter crops and agronomically important perennial grasses have yet to be revealed. Here, two L. perenne plants with contrasting levels of FT, high frost tolerant (HFT) and low frost tolerant (LFT) plants, were selected for comparative proteomic research. The work focused on analyses of leaf protein accumulation before and after 2, 8, 26 h, and 3, 5, 7, 14 and 21 days of CA, using a high-throughput two-dimensional electrophoresis, and on the identification of proteins which were accumulated differentially between the selected plants by the application of mass spectrometry (MS). Analyses of 580 protein profiles revealed a total of 42 (7.2%) spots that showed at a minimum of 1.5-fold differences in protein abundance, at a minimum of at one time point of CA between HFT and LFT genotypes. It was shown that significant differences in profiles of protein accumulation between the analyzed plants appeared most often on the 5th (18 proteins) and the 7th (19 proteins) day of CA. The proteins derived from 35 (83.3%) spots were successfully identified by the use of MS and chloroplast proteins were shown to be the major group selected as differentially accumulated during CA. The functions of the identified proteins and their probable influence on the level of FT in L. perenne are discussed.
Keywords:APX  ascorbate peroxidases  ATP  adenosine triphosphate  CA  cold acclimation  CS  cysteine synthase  2-DE  two-dimensional electrophoresis  ESI  electrospray ionization  Fp  Festuca pratensis  FT  frost tolerance  GS  glutamine synthetase  HFT  high frost tolerant  Hsp  heat shock protein  IEF  isoelectrofocusing  LFT  low frost tolerant  Lp  Lolium perenne  LSR  a large subunit of ribulose-1  5-bisphosphate carboxylase/oxygenase  MALDI-ToF  Matrix Assisted Laser Desorption/Ionization Time of Flight  MS  mass spectrometry  MSDB  Model System Database  MW  molecular weight  PPFD  photosynthetic photon flux density  RuBisCO  ribulose-1  5-bisphosphate carboxylase/oxygenase  RA  RuBisCO activase  RBP  RuBisCO binding protein  ROS  reactive oxygen species  ToF - Q  Time-of-Flight - Quadrupole  % Vol  the normalized volumes  WH  winter-hardiness
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