Detail of Fig1H_MT_DMSO



Project
Title
Time-lapse images of microtubule alignment in Arabidopsis zygote in the presence of DMSO.
Description
Time-lapse images of microtubule alignment in Arabidopsis zygote in the presence of DMSO.
Release, Updated
2024-12-14
License
CC-BY
Kind
Image data
File Formats
.tif
Data size
349.0 MB

Organism
Arabidopsis thaliana ( NCBITaxon:3702 )
Strain(s)
-
Cell Line
-

Datatype
-
Molecular Function (MF)
Biological Process (BP)
cytoskeleton organization ( GO:0007010 )
Cellular Component (CC)
cytoskeleton ( GO:0005856 ) phragmoplast ( GO:0009524 )
Biological Imaging Method
two-photon laser scanning microscopy ( Fbbi:00000254 )
time lapse microscopy ( Fbbi:00000249 )
X scale
0.138 micrometer/pixel
Y scale
0.138 micrometer/pixel
Z scale
1 micrometer/slice
T scale
20 minutes per time interval

Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

Summary of Methods
See details in Kimata Y, et. al. Life Sci Alliance. 2023 Feb 27;6(5):e202201657.
Related paper(s)

Yusuke Kimata, Moe Yamada, Takashi Murata, Keiko Kuwata, Ayato Sato, Takamasa Suzuki, Daisuke Kurihara, Mitsuyasu Hasebe, Tetsuya Higashiyama, Minako Ueda (2023) Novel inhibitors of microtubule organization and phragmoplast formation in diverse plant species., Life science alliance, Volume 6, Number 5

Published in 2023 May (Electronic publication in Feb. 27, 2023, midnight )

(Abstract) Cell division is essential for development and involves spindle assembly, chromosome separation, and cytokinesis. In plants, the genetic tools for controlling the events in cell division at the desired time are limited and ineffective owing to high redundancy and lethality. Therefore, we screened cell division-affecting compounds in Arabidopsis thaliana zygotes, whose cell division is traceable without time-lapse observations. We then determined the target events of the identified compounds using live-cell imaging of tobacco BY-2 cells. Subsequently, we isolated two compounds, PD-180970 and PP2, neither of which caused lethal damage. PD-180970 disrupted microtubule (MT) organization and, thus, nuclear separation, and PP2 blocked phragmoplast formation and impaired cytokinesis. Phosphoproteomic analysis showed that these compounds reduced the phosphorylation of diverse proteins, including MT-associated proteins (MAP70) and class II Kinesin-12. Moreover, these compounds were effective in multiple plant species, such as cucumber (Cucumis sativus) and moss (Physcomitrium patens). These properties make PD-180970 and PP2 useful tools for transiently controlling plant cell division at key manipulation nodes conserved across diverse plant species.

Contact
Minako Ueda , Tohoku University , Graduate School of Life Sciences
Contributors
Yusuke Kimata, Moe Yamada, Takashi Murata

OMERO Dataset
OMERO Project
Source