First published online March 6, 2003; 10.1104/pp.102.016444
Plant Physiol, April 2003, Vol. 131, pp. 1602-1612
Distribution of Fucose-Containing Xyloglucans in Cell Walls of
the mur1 Mutant of Arabidopsis1
Glenn
Freshour,
Christopher
P.
Bonin,2
Wolf-Dieter
Reiter,
Peter
Albersheim,
Alan G.
Darvill, and
Michael G.
Hahn*
The University of Georgia, Complex Carbohydrate Research Center
(G.F., P.A., A.G.D., M.G.H.) and Departments of Plant Biology (M.G.H.)
and Biochemistry and Molecular Biology (P.A., A.G.D.), 220 Riverbend
Road, Athens, Georgia 30602-4712; and University of Connecticut,
Department of Molecular and Cell Biology, Storrs, Connecticut 06269 (C.P.B., W.-D.R.)
The monoclonal antibody, CCRC-M1, which recognizes a fucose
(Fuc)-containing epitope found principally in the cell wall
polysaccharide xyloglucan, was used to determine the distribution of
this epitope throughout the mur1 mutant of
Arabidopsis. Immunofluorescent labeling of whole seedlings
revealed that mur1 root hairs are stained heavily by
CCRC-M1, whereas the body of the root remains unstained or only lightly
stained. Immunogold labeling showed that CCRC-M1 labeling within the
mur1 root is specific to particular cell walls and cell
types. CCRC-M1 labels all cell walls at the apex of primary roots
2 d and older and the apices of mature lateral roots, but does not
bind to cell walls in lateral root initials. Labeling with CCRC-M1
decreases in mur1 root cells that are undergoing rapid
elongation growth such that, in the mature portions of primary and
lateral roots, only the walls of pericycle cells and the outer walls of
epidermal cells are labeled. Growth of the mutant on Fuc-containing
media restores wild-type labeling, where all cell walls are labeled by
the CCRC-M1 antibody. No labeling was observed in mur1
hypocotyls, shoots, or leaves; stipules are labeled. CCRC-M1 does label
pollen grains within anthers and pollen tube walls. These results
suggest the Fuc destined for incorporation into xyloglucan is
synthesized using one or the other or both isoforms of
GDP-D-mannose 4,6-dehydratase, depending on the cell type
and/or developmental state of the cell.
1
This work was supported by the U.S.
Department of Energy (grant nos. DE-FG02-96ER20220 and
DE-FG02-95ER20203) and in part by the U.S. Department of
Energy-funded Center for Plant and Microbial Complex
Carbohydrates (grant no. DE-FG05-93ER20097).
2
Present address: Department of Biochemistry and
Molecular Biophysics, Columbia University, New York, NY 10032.
*
Corresponding author; e-mail hahn{at}ccrc.uga.edu; fax
706-542-4412.
© 2003 American Society of Plant Biologists
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