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First published online May 19, 2006; 10.1104/pp.106.079384 Plant Physiology 141:1035-1044 (2006) © 2006 American Society of Plant Biologists Quantitative Trait Loci Analysis of Primary Cell Wall Composition in Arabidopsis1Laboratoire de Biologie Cellulaire (G.M., S.P., H.H.) and Station de Génétique et d'Amélioration des Plantes (O. Loudet), Institut Jean-Pierre Bourgin, Institute National de la Recherche Agronomique, 78026 Versailles, France; Max Planck Institute for Molecular Plant Physiology, 14476 Golm, Germany (H.W.-W., M.P.); and Faculté des Science, Unité Mixte de Recherche 6037, Centre National de la Recherche Scientifique, European Institute for Peptide Research 23, Université de Rouen, 76821 Mont Saint Aignan cedex, France (M.-P.B., C.R., O. Lerouxel, P.L.)
Quantitative trait loci (QTL) analysis was used to identify genes underlying natural variation in primary cell wall composition in Arabidopsis (Arabidopsis thaliana). The cell walls of dark-grown seedlings of a Bay-0 x Shahdara recombinant inbred line population were analyzed using three miniaturized global cell wall fingerprinting techniques: monosaccharide composition analysis by gas chromatography, xyloglucan oligosaccharide mass profiling, and whole-wall Fourier-transform infrared microspectroscopy. Heritable variation and transgression were observed for the arabinose-rhamnose ratio, xyloglucan side-chain composition (including O-acetylation levels), and absorbance for a subset of Fourier-transform infrared wavenumbers. In total, 33 QTL, corresponding to at least 11 different loci controlling dark-grown hypocotyl length, pectin composition, and levels of xyloglucan fucosylation and O-acetylation, were identified. One major QTL, accounting for 51% of the variation in the arabinose-rhamnose ratio, affected the number of arabinan side chains presumably attached to the pectic polysaccharide rhamnogalacturonan I, paving the way to positional cloning of the first gene underlying natural variation in pectin structure. Several QTL were found to be colocalized, which may have implications for the regulation of xyloglucan metabolism. These results demonstrate the feasibility of combining fingerprinting techniques, natural variation, and quantitative genetics to gain original insight into the molecular mechanisms underlying the structure and metabolism of cell wall polysaccharides.
1 This work was supported by GABI-GENOPLANTE (contract no. AF 2001 091). 2 These authors contributed equally to the paper. 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: Herman Höfte (herman.hofte{at}versailles.inra.fr). Article, publication date, and citation information can be found at www.plantphysiol.org/cgi/doi/10.1104/pp.106.079384. * Corresponding author; e-mail herman.hofte{at}versailles.inra.fr; fax 33130833099. Received February 17, 2006; returned for revision April 28, 2006; accepted April 30, 2006. This article has been cited by other articles:
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