CHARACTERIZATION OF A NOVEL PROTEIN-INDUCED BY PROGRESSIVE OR RAPID DROUGHT AND SALINITY IN BRASSICA-NAPUS LEAVES

被引:72
作者
REVIRON, MP
VARTANIAN, N
SALLANTIN, M
HUET, JC
PERNOLLET, JC
DEVIENNE, D
机构
[1] UNIV PARIS SUD, INRA, GENET VEGETALE STN, CNRS, LA FERME MOULON, F-91190 GIF SUR YVETTE, FRANCE
[2] INST SCI VEGETALES, CNRS, UNITE 40, F-91198 GIF SUR YVETTE, FRANCE
[3] INRA, ETUDE PROT LAB, F-78026 VERSAILLES, FRANCE
关键词
D O I
10.1104/pp.100.3.1486
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Under progressive drought stress, Brassica napus displays differential leaf modifications. The oldest leaves, developed before the onset of water deficit, wilt gradually, whereas the youngest leaves harden. Hardening was distinguished by leaf turgor and bluish wax bloom when the shoot water potential was below -3 MPa and the leaf water saturation deficit was about 60%. This adaptive change was accompanied by modifications in two-dimensional protein profiles. Ten percent of the polypeptides had altered abundance or were unique to drought-stressed plants. Two-dimensional analysis of in vitro translation products did not reveal a general decrease in mRNA population. A 22-kD double polypeptide was increased by progressive or rapid water stress and salinity and disappeared upon rehydration. These polypeptides have a common N-terminal sequence, which does not reveal homology with any known water-stress protein but which contains the signature motif of soybean Kunitz trypsin inhibitors. Immunoprecipitation allowed these polypeptides to be identified on two-dimensional gels of in vitro translation products. They appeared to be synthesized as a 24-kD precursor, and their transcript was present in the control well-watered leaves, where the polypeptides were never detected, indicating a possible translational regulation. A putative function of this protein, named BnD22, in the retardation of drought-induced leaf senescence is discussed.
引用
收藏
页码:1486 / 1493
页数:8
相关论文
共 30 条
[1]  
ASPART L, 1984, PLANT PHYSIOL, V76, P664, DOI 10.1104/pp.76.3.664
[2]   PROSITE - A DICTIONARY OF SITES AND PATTERNS IN PROTEINS [J].
BAIROCH, A .
NUCLEIC ACIDS RESEARCH, 1992, 20 :2013-2018
[3]  
BALESTRINI S, 1983, PHYSIOL VEG, V21, P269
[5]   CHARACTERIZATION OF A RICE GENE SHOWING ORGAN-SPECIFIC EXPRESSION IN RESPONSE TO SALT STRESS AND DROUGHT [J].
CLAES, B ;
DEKEYSER, R ;
VILLARROEL, R ;
VANDENBULCKE, M ;
BAUW, G ;
VANMONTAGU, M ;
CAPLAN, A .
PLANT CELL, 1990, 2 (01) :19-27
[6]   A CDNA-BASED COMPARISON OF DEHYDRATION-INDUCED PROTEINS (DEHYDRINS) IN BARLEY AND CORN [J].
CLOSE, TJ ;
KORTT, AA ;
CHANDLER, PM .
PLANT MOLECULAR BIOLOGY, 1989, 13 (01) :95-108
[7]   A SIMPLIFICATION OF HEUKESHOVEN AND DERNICKS SILVER STAINING OF PROTEINS [J].
DAMERVAL, C ;
LEGUILLOUX, M ;
BLAISONNEAU, J ;
DEVIENNE, D .
ELECTROPHORESIS, 1987, 8 (03) :158-159
[8]   DIFFERENTIAL TWO-DIMENSIONAL PROTEIN-PATTERNS AS RELATED TO TISSUE-SPECIFICITY AND WATER CONDITIONS IN BRASSICA-NAPUS VAR OLEIFERA ROOT-SYSTEM [J].
DAMERVAL, C ;
VARTANIAN, N ;
DEVIENNE, D .
PLANT PHYSIOLOGY, 1988, 86 (04) :1304-1309
[9]  
Dayhoff MO, 1978, ATL PROTEIN SEQ STRU, V5, P345
[10]  
DOWNING WL, 1992, PLANT J, V2, P685, DOI 10.1046/j.1365-313X.1992.t01-11-00999.x