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Researchers Discover Gene Mutation Thought To Control Energy Levels

Main Category: Genetics
Also Included In: Sports Medicine / Fitness;  Diabetes
Article Date: 18 Sep 2007 - 20:00 PST

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University of Ottawa medical researchers have discovered a mutation in a gene that is widely considered to be the major controller of energy levels in our bodies. The discovery has significant implications for people suffering from diabetes and for endurance athletes.

This study focused on the gene for AMPK (adenosine monophosphate-activated protein kinase), which controls the amount of energy in our cells by becoming active when fuel stores start to deplete, such as during exercise. The mutation discovered in individuals from two unrelated families caused a doubling of AMPK activity in muscle during rest, mimicking a state of exercise.

The uOttawa research team led by Drs Mary-Ellen Harper, Robert Dent and Ruth McPherson, in collaboration with researchers in Berkeley California, also found that the mutation produces a decrease in the storage in muscle of fat and an increase in muscle glycogen. The discovery has implications for the treatment of type 2 diabetes, as high levels of fat stored in the muscle have been linked to insulin resistance. In addition, as metformin, a drug commonly used to both prevent and treat diabetes, acts by increasing AMPK activity, this discovery provides valuable information for pharmaceutical research. The findings will also be of great interest to exercise physiologists, as increased muscle glycogen enhances a person's capacity for endurance exercise (e.g., marathon running).

This significant discovery, made possible by grants from the Heart & Stroke Foundation of Ontario and the generous participation of patients and volunteers, is reported in the September 19 issue of the online, open-access journal, PLoS ONE.

Citation: Costford SR, Kavaslar N, Ahituv N, Chaudhry SN, Schackwitz WS, et al (2007) Gain-of-Function R225W Mutation in Human AMPKc3 Causing Increased Glycogen and Decreased Triglyceride in Skeletal Muscle. PLoS ONE 2(9): e903. doi:10.1371/journal.pone.0000903
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PLoS ONE is the first journal of primary research from all areas of science to employ both pre- and post-publication peer review to maximize the impact of every report it publishes. PLoS ONE is published by the Public Library of Science (PLoS), the open access publisher whose goal is to make the world's scientific and medical literature a public resource.

http://www.plosone.org

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