In vivo analysis of cell division, cell growth, and differentiation at the shoot apical meristem in arabidopsis

被引:162
|
作者
Grandjean, O
Vernoux, T
Laufs, P
Belcram, K
Mizukami, Y
Traas, J [1 ]
机构
[1] INRA, Biol Cellulaire Lab, Inst Jean Pierre Bourgin, F-78026 Versailles, France
[2] INRA, Lab Commun Cytol, Inst Jean Pierre Bourgin, F-78026 Versailles, France
[3] Univ Calif Berkeley, Berkeley, CA 94720 USA
来源
PLANT CELL | 2004年 / 16卷 / 01期
关键词
D O I
10.1105/tpc.017962
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
The aerial parts of the plant are generated by groups of rapidly dividing cells called shoot apical meristems. To analyze cell behavior in these structures, we developed a technique to visualize living shoot apical meristems using the confocal microscope. This method, combined with green fluorescent protein marker lines and vital stains, allows us to follow the dynamics of cell proliferation, cell expansion, and cell differentiation at the shoot apex. Using this approach, the effects of several mitotic drugs on meristem development were studied. Oryzalin (depolymerizing microtubules) very rapidly caused cell division arrest. Nevertheless, both cell expansion and cell differentiation proceeded in the treated meristems. Interestingly, DNA synthesis was not blocked, and the meristematic cells went through several rounds of endoreduplication in the presence of the drug. We next treated the meristems with two inhibitors of DNA synthesis, aphidicolin and hydroxyurea. In this case, cell growth and, later, cell differentiation were inhibited, suggesting an important role for DNA synthesis in growth and patterning.
引用
收藏
页码:74 / 87
页数:14
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