Abscisic acid and sucrose increase the protein content in date palm somatic embryos, causing changes in 2-DE profile

被引:26
作者
Sghaier-Hammami, Besma [1 ,2 ]
Jorrin-Novo, Jesus V. [1 ]
Gargouri-Bouzid, Radhia [2 ]
Drira, Noureddine [2 ]
机构
[1] Univ Cordoba, Dept Biochem & Mol Biol, Agr & Plant Biochem & Prote Res Grp, Cordoba, Spain
[2] Fac Sci Sfax, Lab Biotechnol Vegetales Appl Ameliorat Cultures, Sfax, Tunisia
关键词
Date palm proteomics; Embryo proteomics; Phoenix dactylifera L; Somatic embryos; Abscisic acid; Sucrose; 2-DE analysis; PHOENIX-DACTYLIFERA L; DNA TOPOISOMERASE-I; PROTEOMIC ANALYSIS; STORAGE PROTEIN; SUSPENSION-CULTURES; PLANT-REGENERATION; CLUSTER-ANALYSIS; MESSENGER-RNA; DAUCUS-CAROTA; LEAF PROTEOME;
D O I
10.1016/j.phytochem.2010.05.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Various supplements (abscisic acid (ABA) or sucrose) were added to the initial embryo culture medium (M3) with the aim of improving the vigour of vitroplants deriving from date palm somatic embryogenesis. ABA (20 and 40 mu M) and sucrose (90 g/l) applied for 4 and 2 weeks respectively increased embryo thickness, with no apparent difference in length. ABA (5-40 mu M) increased embryo proliferation rate. Somatic embryos maintained in modified M3 (M3 supplemented with ABA and an increased sucrose concentration) contained a higher amount of protein than those maintained in initial M3 (no ABA, 30 g/l of sucrose), with a 1.5-1.7-fold increase depending on the compound and concentration assayed. The 1-D and 2-DE protein profiles showed qualitative and quantitative differences between the somatic embryos cultured in initial M3 (control) and in modified M3. Statistical analysis of spot intensity was performed by principal component analysis, yielding two accurate groups of samples and determining the most discriminating spots. Samples were also clustered using Euclidean distance with an average linkage algorithm. Thirty-four variable spots were identified using mass spectrometry analysis. Identified proteins were classified into the following functional categories: energy metabolism (five proteins); protein translation, folding and degradation (9); redox maintenance (5); cytoskeleton (3); storage protein (2); and with no assigned function as (10). While "up-regulation" of stress-related proteins and "down-regulation" of energy metabolism proteins were observed in somatic embryos matured in M3 supplemented with ABA, storage proteins (legumin) were "up-regulated" in somatic embryos matured in M3 supplemented with increased sucrose. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1223 / 1236
页数:14
相关论文
共 109 条
[1]   BA enhances the germination of oil palm somatic embryos derived from embryogenic suspension cultures [J].
Aberlenc-Bertossi, F ;
Noirot, M ;
Duval, Y .
PLANT CELL TISSUE AND ORGAN CULTURE, 1999, 56 (01) :53-57
[2]   Characterization of glycolytic initial metabolites and enzyme activities in developing sunflower (Helianthus annuus L.) seeds [J].
Adrian Troncoso-Ponce, M. ;
Kruger, Nicholas J. ;
Ratcliffe, George ;
Garces, Rafael ;
Martinez-Force, Enrique .
PHYTOCHEMISTRY, 2009, 70 (09) :1117-1122
[3]   In-depth investigation of the soybean seed-filling proteome and comparison with a parallel study of rapeseed [J].
Agrawal, Ganesh Kumar ;
Hajduch, Martin ;
Graham, Katherine ;
Thelen, Jay J. .
PLANT PHYSIOLOGY, 2008, 148 (01) :504-518
[4]  
Al-Khayri Jameel M., 2005, V77, P309
[5]  
Ammirato P.V., 1987, PLANT TISSUE CELL CU, P57
[6]   EFFECTS OF ABSCISIC-ACID ON DEVELOPMENT OF SOMATIC EMBRYOS FROM CELLS OF CARAWAY (CARUM-CARVI L) [J].
AMMIRATO, PV .
BOTANICAL GAZETTE, 1974, 135 (04) :328-337
[7]   STRUCTURE, PHYSICAL AND CHEMICAL PROPERTIES OF SOY BEAN PROTEIN GLYCININ [J].
BADLEY, RA ;
ATKINSON, D ;
HAUSER, H ;
OLDANI, D ;
GREEN, JP ;
STUBBS, JM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1975, 412 (02) :214-228
[8]  
Balestrazzi A, 2001, EUR J HISTOCHEM, V45, P31
[9]   Cloning of a cDNA encoding DNA topoisomerase I in Daucus carota and expression analysis in relation to cell proliferation [J].
Balestrazzi, A ;
Toscano, I ;
Bernacchia, G ;
Luo, MZ ;
Otte, S ;
Carbonera, D .
GENE, 1996, 183 (1-2) :183-190
[10]  
BARTON KA, 1982, J BIOL CHEM, V257, P6089