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CELLULAR MESSAGING ELUCIDATED
By Sean Henahan, Access Excellence
MADISON (17 July 1997)- The elucidation of a newly discovered
pathway of cellular communication could contribute to new understanding
of cancer and birth defects, report researchers from the University of
Wisconsin-Madison.
Working with fruit flies, research geneticists discovered that a cellular
signaling protein called MAD is responsible for switching genes on or off
by binding directly to DNA, in effect telling the cell to start or
stop a specified task.
"We've shown that the MAD protein is a direct regulator of target gene
transcription in response to a (specific) signal," said lead investigator
Allen Laughon.
By revealing the terminus of the pathway by which cells send and receive
messages, the new discovery forms the basis for the future treatment of
diseases like cancer, and provides a fundamental advance in understanding
a process that triggers decisive events in cells, he said.
The mapping of the communication pathways between cells is a fundamental
quest in modern biology.
Communication -- or miscommunication -- between cells is the basis
for many diseases. For example, in humans it is believed that there are
many layers of genes which act as a group to prevent cancer by blocking
the inappropriate proliferation of cells. But if these "tumor suppression
genes" are defective, cells become blind to messages meant to ward off
runaway cell proliferation. Cancer can be the result.
"As long as cells sense this information, they don't grow out of control,"
Laughon said.
"We've found a mechanism that is really important," said co-investigator
Sean Carroll, a molecular biologist at the Howard Hughes Medical Institute
at UW-Madison. "The universe of genes regulated by this pathway
is very large. I would guess hundreds of genes."
"The missing link," explained Laughon, "has been how the signal switches
genes on or off. This protein shuttles from the inner surface of the cell
membrane right to the DNA, in one fell swoop."
While the discovery is not likely to lead immediately to breakthrough
drugs, it could form the basis for new genetic- based treatments for disease,
he added.
The research appears in the July 17, 1997 issue of Nature.
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