Localization of peroxidase mRNAs in soybean seeds by in situ hybridization

被引:15
作者
Gijzen, M
Miller, SS
Bowman, LA
Batchelor, AK
Boutilier, K
Miki, BLA
机构
[1] Agr & Agri Food Canada, So Crop Protect & Food Res Ctr, London, ON N5V 4T3, Canada
[2] Eastern Cereals & Oilseeds Res Ctr, Ottawa, ON, Canada
关键词
embryo; gene expression; Glycine max; oxidoreductase; seed coat; testa;
D O I
10.1023/A:1006244500951
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
The soybean Ep gene encodes an anionic peroxidase enzyme that accumulates in large amounts in seed coat tissues. We have isolated a second peroxidase gene, Prx2, that is also highly expressed in developing seed coat tissues. Sequence analysis of Prx2 cDNA indicates that this transcript encodes a cationic peroxidase isozyme that is far removed from Ep in peroxidase phylogeny. To determine the expression patterns for these two peroxidases in developing seeds, the abundance and localization of the Ep and Prx2 transcripts were compared by in situ hybridization. Results show the expression of Ep begins in a small number of cells flanking the vascular bundle in the seed coat, spreads to encircle the seed, and then migrates to the hourglass cells as they develop. Expression of Prx2 occurs throughout development in all cell layers of the seed coat, and is also evident in the pericarp and embryo. Nonetheless, the Ep-encoded enzyme accounts for virtually all of the peroxidase activity detected in mature seed coats. The Prx2 enzyme is either insoluble in a catalytically inactive form, or is subject to degradation during seed maturation.
引用
收藏
页码:57 / 63
页数:7
相关论文
共 27 条
[11]  
Gerhartz W., 1990, Enzymes in industry : production and applications
[12]   SOYBEAN SEED COAT PEROXIDASE - A COMPARISON OF HIGH-ACTIVITY AND LOW-ACTIVITY GENOTYPES [J].
GIJZEN, M ;
VANHUYSTEE, R ;
BUZZELL, RI .
PLANT PHYSIOLOGY, 1993, 103 (04) :1061-1066
[13]   A deletion mutation at the ep locus causes low seed coat peroxidase activity in soybean [J].
Gijzen, M .
PLANT JOURNAL, 1997, 12 (05) :991-998
[14]   PURIFICATION AND DEVELOPMENTAL ANALYSIS OF THE MAJOR ANIONIC PEROXIDASE FROM THE SEED COAT OF GLYCINE-MAX [J].
GILLIKIN, JW ;
GRAHAM, JS .
PLANT PHYSIOLOGY, 1991, 96 (01) :214-220
[15]   DIFFERENTIAL EXPRESSION OF PEROXIDASE ISOGENES DURING THE EARLY STAGES OF INFECTION OF THE TROPICAL FORAGE LEGUME STYLOSANTHES HUMILIS BY COLLETOTRICHUM-GLOEOSPORIOIDES [J].
HARRISON, SJ ;
CURTIS, MD ;
MCINTYRE, CL ;
MACLEAN, DJ ;
MANNERS, JM .
MOLECULAR PLANT-MICROBE INTERACTIONS, 1995, 8 (03) :398-406
[16]   Sequence and RT-PCR expression analysis of two peroxidases from Arabidopsis thaliana belonging to a novel evolutionary branch of plant peroxidases [J].
Kjaersgard, IVH ;
Jespersen, HM ;
Rasmussen, SK ;
Welinder, KG .
PLANT MOLECULAR BIOLOGY, 1997, 33 (04) :699-708
[17]   Expression of the tobacco anionic peroxidase gene is tissue-specific and developmentally regulated [J].
Klotz, KL ;
Liu, TTY ;
Liu, L ;
Lagrimini, LM .
PLANT MOLECULAR BIOLOGY, 1998, 36 (04) :509-520
[18]  
MILLER SS, 1999, IN PRESS ANN BOT
[19]   Structure and organ specificity of an anionic peroxidase from Arabidopsis thaliana cell suspension culture [J].
Ostergaard, L ;
Abelskov, AK ;
Mattsson, O ;
Welinder, KG .
FEBS LETTERS, 1996, 398 (2-3) :243-247
[20]  
OUELLET T, 1992, PLANT J, V2, P321