Identification of genes induced in proteoid roots of white lupin under nitrogen and phosphorus deprivation, with functional characterization of a formamidase

被引:18
|
作者
Rath, Mousumi [1 ]
Salas, Jay [1 ]
Parhy, Bandita [1 ]
Norton, Robert [1 ,2 ]
Menakuru, Himabindu [1 ]
Sommerhalter, Monika [3 ]
Hatlstad, Greg [4 ]
Kwon, Jaimyoung [2 ]
Allan, Deborah L. [5 ]
Vance, Carroll P. [4 ,6 ]
Uhde-Stone, Claudia [1 ]
机构
[1] Calif State Univ Hayward, Dept Biol Sci, Hayward, CA 94542 USA
[2] Calif State Univ Hayward, Dept Stat, Hayward, CA 94542 USA
[3] Calif State Univ Hayward, Dept Chem & Biochem, Hayward, CA 94542 USA
[4] Univ Minnesota, Dept Agron & Plant Genet, St Paul, MN 55108 USA
[5] Univ Minnesota, Dept Soil Water & Climate, St Paul, MN 55108 USA
[6] ARS, USDA, Plant Sci Res Unit, St Paul, MN 55108 USA
基金
美国国家卫生研究院;
关键词
Proteoid roots; Cluster roots; Phosphorus deprivation; Nitrogen deprivation; Formamidase; Formate dehydrogenase; White lupin; IRON-DEFICIENCY; CLUSTER ROOTS; ENHANCED EXPRESSION; MICROARRAY ANALYSIS; ALIPHATIC AMIDASE; ALBUS L; METABOLISM; PHOSPHATE; RESPONSES; ARABIDOPSIS;
D O I
10.1007/s11104-010-0373-7
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
White lupin (Lupinus albus L.) is considered a model system for understanding plant acclimation to nutrient deficiency. It acclimates to phosphorus (P) and iron (Fe) deficiency by the development of short, densely clustered lateral roots called proteoid (or cluster) roots; proteoid-root development is further influenced by nitrogen (N) supply. In an effort to better understand proteoid root function under various nutrient deficiencies, we used nylon filter arrays to analyze 2,102 expressed sequence tags (ESTs) from proteoid roots of P-deficient white lupin. These have been previously analyzed for up-regulation in -P proteoid roots, and were here analyzed for up-regulation in proteoid roots of N-deprived plants. We identified a total of 19 genes that displayed up-regulation in proteoid roots under both P and N deprivation. One of these genes showed homology to putative formamidases. The corresponding open reading frame was cloned, overexpressed in E. coli, and the encoded protein was purified; functional characterization of the recombinant protein confirmed formamidase activity. Though many homologues of bacterial and fungal formamidases have been identified in plants, to our knowledge, this is the first report of a functional characterization of a plant formamidase.
引用
收藏
页码:137 / 150
页数:14
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