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Plant Physiol, May 2003, Vol. 132, pp. 263-271
Quantitative Trait Loci and Comparative Genomics of Cereal Cell
Wall Composition1
Samuel P.
Hazen,2
Robin M.
Hawley,3
Georgia L.
Davis,
Bernard
Henrissat, and
Jonathan D.
Walton*
Department of Energy Plant Research Laboratory, Michigan State
University, East Lansing, Michigan 48824 (S.P.H., R.M.H., J.D.W.);
Department of Agronomy, University of Missouri, Columbia, Missouri
65211 (G.L.D.); Architecture et Fonction des Macromolécules
Biologiques, Unité Mixte de Recherche 6098, Centre
National de la Recherche Scientifique, Universités de Marseille I
and II, 31 Chemin Joseph Aiguier, 13402 Marseille cedex 20, France
(B.H.)
Quantitative trait loci (QTLs) affecting sugar composition
of the cell walls of maize (Zea mays) pericarp were
mapped as an approach to the identification of genes involved in cereal
wall biosynthesis. Mapping was performed using the IBM (B73 × Mo17) recombinant inbred line population. There were statistically
significant differences between B73 and Mo17 in content of xylose
(Xyl), arabinose (Ara), galactose (Gal), and glucose. Thirteen QTLs
were found, affecting the content of Xyl (two QTLs), Ara (two QTLs),
Gal (five QTLs), Glc (two QTLs), Ara + Gal (one QTL), and Xyl + Glc
(one QTL). The chromosomal regions corresponding to two of these,
affecting Ara + Gal and Ara on maize chromosome 3, could be aligned
with a syntenic region on rice (Oryza sativa)
chromosome 1, which has been completely sequenced and annotated. The
contiguous P1-derived artificial chromosome rice clones covering
the QTLs were predicted to encode 117 and 125 proteins, respectively.
Two of these genes encode putative glycosyltransferases, displaying
similarity to carbohydrate-active enzyme database family GT4
(galactosyltransferases) or to family GT64 (C-terminal domain of animal
heparan synthases). The results illustrate the potential of using
natural variation, emerging genomic resources, and homeology within the
Poaceae to identify candidate genes involved in the essential process
of cell wall biosynthesis.
1
This work was supported by the U.S. Department
of Energy, Division of Energy Biosciences, by the National Science
Foundation Plant Genome Research Program, and by the European
Commission (grant no. QLK5-CT-2001-00443).
2
Present address: The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037.
3
Present address: Department of Crop and Soil Science,
Oregon State University, Corvallis, OR 97331.
*
Corresponding author; e-mail walton{at}msu.edu; fax
517-353-9168.
© 2003 American Society of Plant Biologists
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