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Time-Sequence Observations of Microtubule Dynamics throughout Mitosis in Living Cell Suspensions of Stable Transgenic Arabidopsis--Direct Evidence for the Origin of Cortical Microtubules at M/G1 Interface--
Author(s) -
Seiichiro Hasezawa,
Katsuya Ueda,
Fumi Kumagai
Publication year - 2000
Publication title -
plant and cell physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.975
H-Index - 152
eISSN - 1471-9053
pISSN - 0032-0781
DOI - 10.1093/pcp/41.2.244
Subject(s) - mitosis , microtubule , microbiology and biotechnology , biology , cell cortex , arabidopsis , transgene , live cell imaging , cortex (anatomy) , arabidopsis thaliana , biophysics , green fluorescent protein , cell , cytoskeleton , genetics , gene , neuroscience , mutant
Transgenic Arabidopsis thaliana, stably expressing a GFP-TUA6 fusion protein, were subcultured in B5 medium supplemented with 2,4-D and BA. In the cell suspensions, the microtubular changes in the mitotic cells could be monitored by time-sequence observations using a time-lapse system of fluorescence microscopy. We have succeeded in following the microtubule (MT) dynamics in living cells throughout mitosis, from the late G2 phase to early G1 phase, and found that, at the M/G1 interface, the cortical MTs were firstly reorganized in the perinuclear regions and then in the cortex, as we had previously suggested (Hasezawa and Nagata 1991, Nagata et al. 1994). The significance of this observation on the origin of cortical MTs is discussed.

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