Real-Time Imaging of Cellulose Reorientation during Cell Wall Expansion in Arabidopsis Roots

被引:310
作者
Anderson, Charles T. [1 ]
Carroll, Andrew [1 ,3 ]
Akhmetova, Laila [1 ]
Somerville, Chris [1 ,2 ]
机构
[1] Univ Calif Berkeley, Energy Biosci Inst, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Plant & Microbial Biol, Berkeley, CA 94720 USA
[3] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
关键词
DIRECT VISUALIZATION; SYNTHASE MUTANT; MULTINET GROWTH; ELONGATION; THALIANA; MICROTUBULES; MICROFIBRILS; ORIENTATION; PLANTS; ORGANIZATION;
D O I
10.1104/pp.109.150128
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Cellulose forms the major load-bearing network of the plant cell wall, which simultaneously protects the cell and directs its growth. Although the process of cellulose synthesis has been observed, little is known about the behavior of cellulose in the wall after synthesis. Using Pontamine Fast Scarlet 4B, a dye that fluoresces preferentially in the presence of cellulose and has excitation and emission wavelengths suitable for confocal microscopy, we imaged the architecture and dynamics of cellulose in the cell walls of expanding root cells. We found that cellulose exists in Arabidopsis (Arabidopsis thaliana) cell walls in large fibrillar bundles that vary in orientation. During anisotropic wall expansion in wild-type plants, we observed that these cellulose bundles rotate in a transverse to longitudinal direction. We also found that cellulose organization is significantly altered in mutants lacking either a cellulose synthase subunit or two xyloglucan xylosyltransferase isoforms. Our results support a model in which cellulose is deposited transversely to accommodate longitudinal cell expansion and reoriented during expansion to generate a cell wall that is fortified against strain from any direction.
引用
收藏
页码:787 / 796
页数:10
相关论文
共 34 条
[11]   Growth of the plant cell wall [J].
Cosgrove, DJ .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (11) :850-861
[12]  
Desnos T, 1996, DEVELOPMENT, V122, P683
[13]   The maize primary cell wall microfibril: A new model derived from direct visualization [J].
Ding, SY ;
Himmel, ME .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2006, 54 (03) :597-606
[14]  
DOLAN L, 1993, DEVELOPMENT, V119, P71
[15]   Use of the pressure probe in studies of stomatal function [J].
Franks, PJ .
JOURNAL OF EXPERIMENTAL BOTANY, 2003, 54 (387) :1495-1504
[16]   MULTINET GROWTH IN THE CELL WALL OF NITELLA [J].
GREEN, PB .
JOURNAL OF BIOPHYSICAL AND BIOCHEMICAL CYTOLOGY, 1960, 7 (02) :289-&
[17]   Two new fluorescent dyes applicable for visualization of fungal cell walls [J].
Hoch, HC ;
Galvani, CD ;
Szarowski, DH ;
Turner, JN .
MYCOLOGIA, 2005, 97 (03) :580-588
[18]   Cell-wall structure and anisotropy in procuste, a cellulose synthase mutant of Arabidopsis thaliana [J].
MacKinnon, Iain M. ;
Sturcova, Adriana ;
Sugimoto-Shirasu, Keiko ;
His, Isabelle ;
McCann, Maureen C. ;
Jarvis, Michael C. .
PLANTA, 2006, 224 (02) :438-448
[19]   Cell wall extension results in the coordinate separation of parallel microfibrils: evidence from scanning electron microscopy and atomic force microscopy [J].
Marga, F ;
Grandbois, M ;
Cosgrove, DJ ;
Baskin, TI .
PLANT JOURNAL, 2005, 43 (02) :181-190
[20]  
MCCANN MC, 1990, J CELL SCI, V96, P323