From the Ehrhardt Lab, April, 2003
Real-time imaging reveals the dynamic architecture of plant cells
All animal, fungal and plant cells feature guide-wire-like structures called
microtubules, which help move chromosomes into two daughter cells, direct the
movement of other organelles within the cell, and create a framework for cell
shape and movement. Microtubules are semi-rigid, hollow polymers, or long-chain
molecules. In animal cells, they are formed into arrays that radiate from the
cell's center to its surface by a centralized organelle that both creates new
polymers and hangs onto their ends. In plant cells, most microtubules are arranged
quite differently. Instead of having their ends being gathered in the center
of the cell, the polymers create an organized shell over the inside surface,
or cortex, of the cell. "For years, scientists have been trying to figure out
how these cortical arrays are created and become organized", remarked researcher
David Ehrhardt of the Department of Plant Biology of the Carnegie Institution
in Palo Alto, California. "Now by tagging them with the green fluorescent protein
(GFP), we have been able to watch this process in action in living plant cells."
The work, which was conducted by scientists at Carnegie and Stanford University,
determined where many microtubules originate and how some of them move around
to become organized in epidermal cells. The results are published in the April
24, 2003, Science Express .

Figure legend: Confocal image of microtubules in an Arabidopsis cell
expressing a tubulin:GFP fusion protein. The dark horizontal
line was created by bleaching the fusion protein with a laser. Although the
microtubules migrated across the cell cortex, the bleached marks remained stationary.
This experiment revealed that the motility of Arabidopsis cortical microtubules
is not caused by the activity of molecular motors, but by polymer treadmilling,
the net addition of polymer subunits at one end and removal at the opposite
end.
The scientists were able to image individual microtubules in a transgenic plant
of the mustard family, Arabidopsis. They took images at 2 to 5-second
intervals for between 3 and 6 minutes. "We found that most of the new microtubules
are probably born at multiple sites directly at the cortex and are not formed
elsewhere and transferred there," said Ehrhardt. "As we watched individual polymers,
it became clear that cortical sites of initiation often did not hang onto the
ends of the polymers but released them, after which they migrated around by
growing at their leading ends and slowly shortening their lagging ends. This
movement is caused entirely by polymerization activity--the addition and deletion
of molecules in the chain. The microtubules didn't slide around to get where
they were going." The researchers observed migration by polymerization activity
of individual microtubules as they moved into bundles with other microtubules.
This is a new view of how microtubules in the cortical arrays can be repositioned
to contribute to array organization.
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