pubmed-article:16926158 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16926158 | lifeskim:mentions | umls-concept:C0032098 | lld:lifeskim |
pubmed-article:16926158 | lifeskim:mentions | umls-concept:C0009015 | lld:lifeskim |
pubmed-article:16926158 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
pubmed-article:16926158 | lifeskim:mentions | umls-concept:C0001128 | lld:lifeskim |
pubmed-article:16926158 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
pubmed-article:16926158 | pubmed:issue | 43 | lld:pubmed |
pubmed-article:16926158 | pubmed:dateCreated | 2006-10-23 | lld:pubmed |
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pubmed-article:16926158 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16926158 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16926158 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16926158 | pubmed:abstractText | Graminaceous plants have evolved a unique mechanism to acquire iron through the secretion of a family of small molecules, called mugineic acid family phytosiderophores (MAs). All MAs are synthesized from l-Met, sharing the same pathway from l-Met to 2'-deoxymugineic acid (DMA). DMA is synthesized through the reduction of a 3''-keto intermediate by deoxymugineic acid synthase (DMAS). We have isolated DMAS genes from rice (OsDMAS1), barley (HvDMAS1), wheat (TaD-MAS1), and maize (ZmDMAS1). Their nucleotide sequences indicate that OsDMAS1 encodes a predicted polypeptide of 318 amino acids, whereas the other three orthologs all encode predicted polypeptides of 314 amino acids and are highly homologous (82-97.5%) to each other. The DMAS proteins belong to the aldo-keto reductase superfamily 4 (AKR4) but do not fall within the existing subfamilies of AKR4 and appear to constitute a new subfamily within the AKR4 group. All of the proteins showed DMA synthesis activity in vitro. Their enzymatic activities were highest at pH 8-9, consistent with the hypothesis that DMA is synthesized in subcellular vesicles. Northern blot analysis revealed that the expression of each of the above DMAS genes is up-regulated under iron-deficient conditions in root tissue, and that of the genes OsDMAS1 and TaDMAS1 is up-regulated in shoot tissue. OsDMAS1 promoter-GUS analysis in iron-sufficient roots showed that its expression is restricted to cells participating in long distance transport and that it is highly up-regulated in the entire root under iron-deficient conditions. In shoot tissue, OsDMAS1 promoter drove expression in vascular bundles specifically under iron-deficient conditions. | lld:pubmed |
pubmed-article:16926158 | pubmed:language | eng | lld:pubmed |
pubmed-article:16926158 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16926158 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:16926158 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16926158 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16926158 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16926158 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16926158 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16926158 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16926158 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16926158 | pubmed:month | Oct | lld:pubmed |
pubmed-article:16926158 | pubmed:issn | 0021-9258 | lld:pubmed |
pubmed-article:16926158 | pubmed:author | pubmed-author:NakanishiHiro... | lld:pubmed |
pubmed-article:16926158 | pubmed:author | pubmed-author:MoriSatoshiS | lld:pubmed |
pubmed-article:16926158 | pubmed:author | pubmed-author:NishizawaNaok... | lld:pubmed |
pubmed-article:16926158 | pubmed:author | pubmed-author:TakahashiMich... | lld:pubmed |
pubmed-article:16926158 | pubmed:author | pubmed-author:BashirKhurram... | lld:pubmed |
pubmed-article:16926158 | pubmed:author | pubmed-author:NagasakaSeiji... | lld:pubmed |
pubmed-article:16926158 | pubmed:author | pubmed-author:InoueHaruhiko... | lld:pubmed |
pubmed-article:16926158 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16926158 | pubmed:day | 27 | lld:pubmed |
pubmed-article:16926158 | pubmed:volume | 281 | lld:pubmed |
pubmed-article:16926158 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16926158 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16926158 | pubmed:pagination | 32395-402 | lld:pubmed |
pubmed-article:16926158 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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pubmed-article:16926158 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:16926158 | pubmed:articleTitle | Cloning and characterization of deoxymugineic acid synthase genes from graminaceous plants. | lld:pubmed |
pubmed-article:16926158 | pubmed:affiliation | Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657. | lld:pubmed |
pubmed-article:16926158 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16926158 | pubmed:publicationType | Comparative Study | lld:pubmed |
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