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Houston.
Researchers at the University of Texas-Houston Health Science Center
and the University of Chicago announced the discovery of a gene
linked to the risk of Type 2 diabetes.
"It’s
the first time a group has taken a view of the entire human genome
and successfully identified one such gene," said researcher
Graeme Bell, Ph.D., Louis Block professor of biochemistry, molecular
biology and medicine at the University of Chicago.
Bell
is an investigator in the Howard Hughes Medical Institute at the
University of Chicago.
The
research drew on data from Mexican-American residents of Starr County.
After a decade of collaboration, the rsearchers discovered CAPN10,
a gene that accounts for 14 percent of the prevalence of Type 2
diabetes in Mexican Americans and about 4 percent in Europeans.
"It
defines a new biochemical pathway that is involved in the regulation
of blood glucose levels," Bell said.
The
gene interacts with other genes and environmental factors and has
a small effect, but should hold the key to a greater understanding
of the genetic components of Type 2 diabetes and facilitate faster
discovery of other genes, said researcher Craig Hanis, Ph.D., professor
of biological sciences at UT-Houston HSC.
"We
believe that this is a pathway that we can exploit for treatment
that we didn’t know about before," Hanis said.
The
findings were published in the October issue of Nature Genetics.
Type
2 diabetes, also known as adult onset diabetes and noninsulin-dependent
diabetes, affects 15 million Americans and is the seventh leading
cause of death in the United States.
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