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Device
Allows Scientists To Control Gene Activity Across Generations Of
Cells
Friday, February 29, 2008
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Pausing
Cell Division
Using
a new device, scientists administer pulses of a
gene-regulating chemical to budding yeast cells as they
multiply. With each pulse (indicated by orange segments in
the time line), the cells suddenly stop dividing, resuming
only when the pulse stops.
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Credit:
Rockefeller University
Just as cells inherit
genes, they also inherit a set of instructions that tell genes
when to become active, in which tissues and to what extent. Now,
Rockefeller University researchers have built a device that, by
allowing scientists to turn genes on and off in actively
multiplying budding yeast cells, will help them figure out more
precisely than before how genes and proteins interact with one
another and how these interactions drive cellular functions.
“A
slight disturbance in the abundance of a single protein can
affect the functioning of a cell dramatically,”says Gilles
Charvin, a postdoc who works with both Eric Siggia, head of the
Laboratory of Theoretical Condensed
of the Laboratory of Yeast
Molecular Genetics. “So, we wanted to devise a way to
supply a single cell with a controlled pulse of protein at any
time and then see how the cell would respond,”he
says.
Although scientists have had the tools to track
single cells and measure the protein levels within them, the new
device allows scientists to track them for a longer period of
time while not only monitoring but also controlling the activity
of genes. The precision with which the device can track single
cells also allows scientists to construct pedigrees, making it
possible to compare gene activity from one cell to the next.
The
device relies on electrovalves to control a flow of media, which
travels through a tube and then diffuses across a porous membrane
to reach the budding yeast cells. The cells are clamped between
this membrane and a soft material, which forces them to bud
horizontally without damage.
“That was the major
design hurdle,” says Charvin. “To create a device in
which cells don’t move, so that you can track hundreds of
single cells for a long time — about eight rounds of cell
division — which typically lasts 12 hours.”
In
order to induce the activity of a gene, the researchers used
inducer molecules that diffuse through the cell membrane and
control DNA segments called promoters. The molecule’s
presence silences the promoter, which silences the expression of
the gene; the molecule’s absence, on the other hand,
activates the promoter, which activates the gene to crank up the
molecule’s production.
By exploiting this principle,
the scientists showed that they could successfully turn specific
genes on and off by controlling the flow of an inducer molecule
called methionine. They observed that pulses as short as 10
minutes led to changes in protein levels that could be
measured.
The group used this device to study the cell
cycle by putting a gene that must be expressed for cells to
divide under the control of the methionine promoter, and showed
that budding yeast cells would stop and start dividing in perfect
synchrony with alternating pulses of media that did and didn’t
contain methionine. “Like slaves, the cells relied on the
external pulse we gave them to figure out what to do next,”
says Charvin. “We thought this was a pretty striking
illustration of the capabilities of this device.”
Source:
Rockefeller University

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