Overexpression of the ASN1 gene enhances nitrogen status in seeds of Arabidopsis

被引:156
作者
Lam, HM [1 ]
Wong, P
Chan, HK
Yam, KM
Chen, L
Chow, CM
Coruzzi, GM
机构
[1] Chinese Univ Hong Kong, Dept Biol, Shatin, Hong Kong, Peoples R China
[2] NYU, Dept Biol, New York, NY 10003 USA
关键词
D O I
10.1104/pp.103.020123
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
In wild-type Arabidopsis, levels of ASN1 mRNA and asparagine (Asn) are tightly regulated by environmental factors and metabolites. Because Asn serves as an important nitrogen storage and transport compound used to allocate nitrogen resources between source and sink organs, we tested whether overexpression of the major expressed gene for Asn synthetase, ASN1, would lead to changes in nitrogen status in the ultimate storage organ for metabolites-seeds. Transgenic Arabidopsis constitutively overexpressing ASN1 under the cauliflower mosaic virus 35S promoter were constructed (35S-ASN1). In seeds of the 35S-ASN1 lines, three observations support the notion that the nitrogen status was enhanced: (a) elevations of soluble seed protein contents, (b) elevations of total protein contents from acid-hydrolyzed seeds, and (c) higher tolerance of young seedlings when grown on nitrogen-limiting media. Besides quantitative differences, changes in the relative composition of the seed amino acid were also observed. The change in seed nitrogen status was accompanied by an increase of total free amino acids (mainly Asn) allocated to flowers and developing siliques. In 35S-ASN1 lines, sink tissues such as flowers and developing siliques exhibit a higher level of free Asn than source tissues such as leaves and stems, despite significantly higher levels of ASN1 mRNA observed in the source tissues. This was at least partially due to an enhanced transport of Asn from source to sink via the phloem, as demonstrated by the increased levels of Asn in phloem exudates of the 35S-ASN1 plants.
引用
收藏
页码:926 / 935
页数:10
相关论文
共 42 条
[1]  
Bechtold N, 1993, ARABIDOPSIS PROTOCOL, P259
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]   ECTOPIC OVEREXPRESSION OF ASPARAGINE SYNTHETASE IN TRANSGENIC TOBACCO [J].
BREARS, T ;
LIU, C ;
KNIGHT, TJ ;
CORUZZI, GM .
PLANT PHYSIOLOGY, 1993, 103 (04) :1285-1290
[4]   BIOLOGICAL NITROGEN-FIXATION [J].
BURRIS, RH ;
ROBERTS, GP .
ANNUAL REVIEW OF NUTRITION, 1993, 13 :317-335
[5]   Metabolic regulation of asparagine synthetase gene expression in maize (Zea mays L) root tips [J].
Chevalier, C ;
Bourgeois, E ;
Just, D ;
Raymond, P .
PLANT JOURNAL, 1996, 9 (01) :1-11
[6]   THE MOLECULAR-GENETICS OF NITRATE ASSIMILATION IN FUNGI AND PLANTS [J].
CRAWFORD, NM ;
ARST, HN .
ANNUAL REVIEW OF GENETICS, 1993, 27 :115-146
[7]   Sugar regulation of harvest-related genes in asparagus [J].
Davies, KM ;
Seelye, JF ;
Irving, DE ;
Borst, WM ;
Hurst, PL ;
King, GA .
PLANT PHYSIOLOGY, 1996, 111 (03) :877-883
[8]   Host-root exudates increase gene expression of asparagine synthetase in the roots of a hemiparasitic plant Triphysaria versicolor (Scrophulariaceae) [J].
Delavault, P ;
Estabrook, E ;
Albrecht, H ;
Wrobel, R ;
Yoder, JI .
GENE, 1998, 222 (02) :155-162
[9]   THE AMINO-ACID POOL OF HIGH AND LOW PROTEIN RYE INBRED LINES (SECALE-CEREALE L) [J].
DEMBINSKI, E ;
BANY, S .
JOURNAL OF PLANT PHYSIOLOGY, 1991, 138 (04) :494-496
[10]  
Dembinski E, 1996, PHYSIOL PLANTARUM, V96, P66, DOI 10.1111/j.1399-3054.1996.tb00184.x