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First published online September 20, 2007; 10.1104/pp.107.107326 Plant Physiology 145:601-615 (2007) © 2007 American Society of Plant Biologists OPEN ACCESS ARTICLE
Early Steps in Proanthocyanidin Biosynthesis in the Model Legume Medicago truncatula1,[W],[OA]Plant Biology Division (Y.P., G.J.P., R.A.D.) and Forage Improvement Division (E.W., Z.W.), Samuel Roberts Noble Foundation, Ardmore, Oklahoma 73401
Oligomeric proanthocyanidins (PAs) composed primarily of epicatechin units accumulate in the seed coats of the model legume Medicago truncatula, reaching maximal levels at around 20 d after pollination. Genes encoding the single Medicago anthocyanidin synthase (ANS; EC 1.14.11.19) and leucoanthocyanidin reductase (LAR; EC 1.17.1.3) were cloned and the corresponding enzymes functionally identified. Recombinant MtANS converted leucocyanidin to cyanidin, and, more efficiently, dihydroquercetin to the flavonol quercetin. Levels of transcripts encoding dihydroflavonol reductase, ANS, and anthocyanidin reductase (ANR), the enzyme responsible for conversion of anthocyanidin to (–)-epicatechin, paralleled the accumulation of PAs in developing seeds, whereas LAR transcripts appeared to be more transiently expressed. LAR, ANS, and ANR proteins were localized to the cytosol in transfected tobacco (Nicotiana tabacum) leaves. Antisense down-regulation of ANS in M. truncatula resulted in reduced anthocyanin and PA levels, but had no impact on flavonol levels. Transgenic tobacco plants constitutively overexpressing MtLAR showed reduced anthocyanin content, but no catechin or increased levels of PAs were detected either in leaves or in flowers. Our results confirm previously ascribed in vivo functions for ANS and ANR. However, the apparent lack of catechin in M. truncatula PAs, the poor correlation between LAR expression and PA accumulation, and the lack of production of catechin monomers or oligomers in transgenic plants overexpressing MtLAR question the role of MtLAR in PA biosynthesis in Medicago.
1 This work was supported by the Samuel Roberts Noble Foundation and Forage Genetics International. The confocal microscope used in this study was funded by the National Science Foundation (equipment grant no. DBI–0400580). The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Richard A. Dixon (radixon{at}noble.org). [W] The online version of this article contains Web-only data. [OA] Open Access articles can be viewed online without a subscription. www.plantphysiol.org/cgi/doi/10.1104/pp.107.107326 * Corresponding author; e-mail radixon{at}noble.org. Received August 13, 2007; accepted September 6, 2007; published September 20, 2007.
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