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Obesity-related gene in mouse discovered at ORNL
The gene was discovered by Madhu Dhar,
postdoctoral fellow from the University of Tennessee who works in the laboratory of
Life Sciences Division's Dabney Johnson. Dhar's research was funded by the National
Institutes of Health, and the findings were published in a paper in a recent issue of
Physiological Genomics.
"We have found that the normal mouse has a gene on chromosome 7
that probably plays a role in the transport of fat from the blood into fat
cells, where fat is stored as a source of energy to keep the body
healthy," Johnson says. "If a mutant form of this gene is inherited from
the mother in certain genetic backgrounds, the offspring grow 35 to 50 percent fatter by
middle age than does a normal mouse, even though they are eating food low in fat."
Unlike some known mouse obesity genes that can act all alone to cause excessive body
fat, the ORNL researchers have shown that the chromosome 7 gene must act in concert
with other genes involved in maintaining the body's energy balance. If female mice
possessing this mutated gene are mated with males having different genetic
backgrounds, the offspring may not become obese, suggesting they have genes that
code for proteins that suppress fat accumulation. Humans and mice are genetically
similar and produce similar proteins. In humans, chromosome 15 is similar to
chromosome 7 in the mouse.
The ORNL group has been focusing on
chromosome 7 in the mouse for some time. In the
1950s ORNL geneticists Bill and Liane Russell
irradiated mice and observed that some of their
offspring who survived had a pinkish coat and
pink eyes instead of normal gray-brown fur
pigmentation and dark eyes. It was later
determined that the radiation knocked out DNA
from a coat-color gene, called the pink-eye
marker (p), on mouse chromosome 7.
Neighboring genes also were deleted or altered in
some irradiated mice, and the defects were passed
on.
Thanks to the availability of improved
technologies, ORNL researchers have defined the
small region on mouse chromosome 7 that
contains the p gene and its neighbors. Using
recombinant DNA techniques, they identified and
characterized genes from this small region in the
normal mouse. And in mutant mice they have
identified behavioral oddities, internal defects, and
disorders such as epilepsy and obesity caused by the absence or alteration of certain
neighboring genes on chromosome 7. From this information on genetic material gone
awry, they can determine the function of the normal genes in this chromosome region.
Johnson says that, like humans, mice deposit fat in their bodies in
different patterns that are genetically controlled. The distribution of fat
deposits in mice with the obesity-related gene has been observed in
three dimensions by Mike Paulus and Shaun Gleason in ORNL's
Instrumentation and Controls Division (see MicroCAT "Sees" Hidden
Mouse Defects). They have imaged internal fat deposits in mice using
the MicroCAT miniature X-ray computerized tomography system they
developed. Using special software, they have determined the size and
weight of those fat deposits.
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