Cytokinesis and building of the cell plate in plants

被引:128
作者
Verma, DPS [1 ]
机构
[1] Ohio State Univ, Dept Mol Genet, Columbus, OH 43210 USA
[2] Ohio State Univ, Ctr Plant Biotechnol, Columbus, OH 43210 USA
来源
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY | 2001年 / 52卷
关键词
cell division; phragmoplast; vesicle fusion; callose synthase; plant cytoskeleton; cell wall; phragmoplastin; exocytosis;
D O I
10.1146/annurev.arplant.52.1.751
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytokinesis in plant cells is more complex than in animals, as it involves building a cell plate as the final step in generating two cells. The cell plate is built in the center of phragmoplast by fusion of Golgi-derived vesicles. This step imposes an architectural problem where ballooning of the fused structures has to be avoided to create a plate instead. This is apparently achieved by squeezing the vesicles into dumbbell-shaped vesicle-tubule-vesicle (VTV) structures with the help of phragmoplastin, a homolog of dynamin. These structures are fused at their ends in a star-shaped body creating a tubulovesicular "honeycomb-like" structure sandwiched between the positive ends of the phragmoplast microtubules. This review summarizes our current understanding of various mechanisms involved in budding-off of Golgi vesicles, delivery and fusion of vesicles to initiate cell plate, and the synthesis of polysaccharides at the forming cell plate. Little is known about the molecular mechanisms involved in determining the site, direction, and the point of attachment of the growing cell plate with the parental cell wall. These gaps may be filled soon, as many genes that have been identified by mutations are analyzed and functions of their products are deciphered.
引用
收藏
页码:751 / 784
页数:38
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