Molecular basis of seed lipoxygenase null traits in soybean line OX948

被引:15
作者
Reinprecht, Yarmilla [1 ]
Luk-Labey, Shun-Yan [1 ]
Yu, Kangfu [3 ]
Poysa, Vaino W. [3 ]
Rajcan, Istvan [1 ]
Ablett, Gary R. [2 ]
Pauls, K. Peter [1 ]
机构
[1] Univ Guelph, Dept Plant Agr, Guelph, ON N1G 2W1, Canada
[2] Univ Guelph, Ridgetown, ON N0P 2C0, Canada
[3] Agr & Agri Food Canada, Greenhouse & Proc Crops Res Ctr, Harrow, ON N0R 1G0, Canada
关键词
LOW LINOLENIC ACID; HISTIDINE-RESIDUES; IRON-BINDING; ARABIDOPSIS; INHERITANCE; GENE; ISOZYMES; MUTANTS; LACKING; IDENTIFICATION;
D O I
10.1007/s00122-011-1528-5
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
The poor stability and off-flavors of soybean oil and protein products can be reduced by eliminating lipoxygenases from soybean seed. Mature seeds of OX948, a lipoxygenase triple null mutant line, do not contain lipoxygenase proteins. The objective of this study was to determine the molecular basis of the seed lipoxygenase null traits in OX948. Comparisons of the sequences for lipoxygenase 1 (Lx1) and lipoxygenase 2 (Lx2) genes in the mutant (OX948) with those in a line with normal lipoxygenase levels (RG10) showed that the mutations in these genes affected a highly conserved group of six histidines necessary for enzymatic activity. The OX948 mutation in Lx1 is a 74 bp deletion in exon 8, which introduces a stop codon that prematurely terminates translation. A single T-A substitution in Lx2 changes histidine H532 (one of the iron-binding ligands essential for L-2 activity) to glutamine. The mutation in the lipoxygenase 3 (Lx3) gene in OX948 is in the promoter region and represents two single base substitutions in a cis-acting AAATAC paired box. All three mutations would result in the loss of lipoxygenase activity in mature seed. The seed lipoxygenase gene mutation-based molecular markers could be used to accelerate and simplify breeding efforts for soybean cultivars with improved flavor.
引用
收藏
页码:1247 / 1264
页数:18
相关论文
共 52 条
[1]  
Axelrod B., 1981, METHODS ENZYMOLOGY, V71, P441, DOI [10.1016/0076-6879(81)71055-3, DOI 10.1016/0076-6879(81)71055-3]
[2]   Analysis of fast neutron-generated mutants at the Arabidopsis thaliana HY4 locus [J].
Bruggemann, E ;
Handwerger, K ;
Essex, C ;
Storz, G .
PLANT JOURNAL, 1996, 10 (04) :755-760
[3]   Multiple sequence alignment with the Clustal series of programs [J].
Chenna, R ;
Sugawara, H ;
Koike, T ;
Lopez, R ;
Gibson, TJ ;
Higgins, DG ;
Thompson, JD .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3497-3500
[4]  
Chopra VL, 2005, CURR SCI INDIA, V89, P353
[5]  
Doyle JJ., 1987, FOCUS, V19, P11, DOI DOI 10.2307/2419362
[6]   The lipoxygenase pathway [J].
Feussner, I ;
Wasternack, C .
ANNUAL REVIEW OF PLANT BIOLOGY, 2002, 53 :275-297
[7]   SoyBase, the USDA-ARS soybean genetics and genomics database [J].
Grant, David ;
Nelson, Rex T. ;
Cannon, Steven B. ;
Shoemaker, Randy C. .
NUCLEIC ACIDS RESEARCH, 2010, 38 :D843-D846
[8]  
HAJIKA M, 1991, JPN J BREED, V41, P507
[9]   2 SOYBEAN GENOTYPES LACKING LIPOXYGENASE-1 [J].
HILDEBRAND, DF ;
HYMOWITZ, T .
JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 1981, 58 (05) :583-586
[10]   CTR1, A NEGATIVE REGULATOR OF THE ETHYLENE RESPONSE PATHWAY IN ARABIDOPSIS, ENCODES A MEMBER OF THE RAF FAMILY OF PROTEIN-KINASES [J].
KIEBER, JJ ;
ROTHENBERG, M ;
ROMAN, G ;
FELDMANN, KA ;
ECKER, JR .
CELL, 1993, 72 (03) :427-441