Changes in the tobacco leaf apoplast proteome in response to salt stress

被引:179
作者
Dani, V
Simon, WJ
Duranti, M
Croy, RRD
机构
[1] Univ Milan, Dept Agrifood Mol Sci, I-20133 Milan, Italy
[2] Univ Durham, Sch Biol & Biomed Sci, Durham, England
关键词
apoplast proteins; salt stress; tobacco leaf; two-dimensional gel electrophoresis; vacuum infiltration;
D O I
10.1002/pmic.200401119
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The apoplast of plant cells is a dynamic compartment involved in many processes, including maintenance of tissue shape, development, nutrition, signalling, detoxification and defence. In this work we used Nicotiana tabacum plants as a model to investigate changes in the soluble apoplast composition induced in response to salt stress. Apoplastic fluid was extracted from leaves of control plants and plants exposed to salt stress, using a vacuum infiltration procedure. Two-dimension electrophoretic analyses revealed about 150 polypeptide spots in the pH range of 3.0 to 10.0, in independent protein extracts, with a high level of reproducibility between the two sample sets. Quantitative evaluation and statistical analyses of the resolved spots in treated and untreated samples revealed 20 polypeptides whose abundance changed in response to salt stress. Mass spectroscopic peptide separation and sequencing was used to identify polypeptides affected by salt stress. While the levels of some proteins were reduced by salt-treatment, an enhanced accumulation of protein species known to be induced by biotic and abiotic stresses was observed. In particular, two chitinases and a germin-like protein increased significantly and two lipid transfer proteins were expressed entirely de novo. Some apoplastic polypeptides, involved in cell wall modifications during plant development, remained largely unchanged. The significance of these components is discussed in the context of stress responses in plants.
引用
收藏
页码:737 / 745
页数:9
相关论文
共 64 条
[31]   APOPLASTIC PH AND AMMONIUM CONCENTRATION IN LEAVES OF BRASSICA-NAPUS L [J].
HUSTED, S ;
SCHJOERRING, JK .
PLANT PHYSIOLOGY, 1995, 109 (04) :1453-1460
[32]   Characterization of expression, and cloning, of β-D-xylosidase and α-L-arabinofuranosidase in developing and ripening tomato (Lycopersicon esculentum Mill.) fruit [J].
Itai, A ;
Ishihara, K ;
Bewley, JD .
JOURNAL OF EXPERIMENTAL BOTANY, 2003, 54 (393) :2615-2622
[33]   Use of SAGE technology to reveal changes in gene expression in Arabidopsis leaves undergoing cold stress [J].
Jung, SH ;
Lee, JY ;
Lee, DH .
PLANT MOLECULAR BIOLOGY, 2003, 52 (03) :553-567
[34]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[35]   MOLECULAR-CLONING OF COMPLEMENTARY-DNA ENCODING THE LIGNIN-FORMING PEROXIDASE FROM TOBACCO - MOLECULAR ANALYSIS AND TISSUE-SPECIFIC EXPRESSION [J].
LAGRIMINI, LM ;
BURKHART, W ;
MOYER, M ;
ROTHSTEIN, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7542-7546
[36]   GERMIN - COMPARTMENTATION OF 2 FORMS OF THE PROTEIN BY WASHING GROWING WHEAT EMBRYOS [J].
LANE, BG ;
GRZELCZAK, ZF ;
KENNEDY, TD ;
KAJIOKA, R ;
ORR, J ;
DAGOSTINO, S ;
JAIKARAN, A .
BIOCHEMISTRY AND CELL BIOLOGY, 1986, 64 (10) :1025-1037
[37]  
LANE BG, 1993, J BIOL CHEM, V268, P12239
[38]   OXALATE, GERMIN, AND THE EXTRACELLULAR-MATRIX OF HIGHER-PLANTS [J].
LANE, BG .
FASEB JOURNAL, 1994, 8 (03) :294-301
[39]  
Levit J., 1980, Responses of Plants to Environmental Stresses. Volume II-Water, Radiation, Salt, VII, P365
[40]   PROMOTER OF A LIPID TRANSFER PROTEIN GENE EXPRESSED IN BARLEY ALEURONE CELLS CONTAINS SIMILAR MYB AND MYC RECOGNITION SITES AS THE MAIZE BZ-MCC ALLELE [J].
LINNESTAD, C ;
LONNEBORG, A ;
KALLA, R ;
OLSEN, OA .
PLANT PHYSIOLOGY, 1991, 97 (02) :841-843