- News Home
5 December 2013 11:26 am ,
Vol. 342 ,
An animal rights group known as the Nonhuman Rights Project filed lawsuits in three New York courts this week in an...
Researchers have been hot on the trail of the elusive Denisovans, a type of ancient human known only by their DNA and...
Thousands of scientists in the Russian Academy of Sciences (RAS) are about to lose their jobs as a result of the...
Dyslexia, a learning disability that hinders reading, hasn't been associated with deficits in vision, hearing, or...
Exotic, elusive, and dangerous, snakes have fascinated humankind for millennia. They can be hard to find, yet their...
Researchers have sequenced and analyzed the first two snake genomes, which represent two evolutionary extremes. The...
Snake venoms are remarkably complex mixtures that can stun or kill prey within minutes. But more and more researchers...
At age 30, Dutch biologist Freek Vonk has built up a respectable career as a snake scientist. But in his home country,...
- 5 December 2013 11:26 am , Vol. 342 , #6163
- About Us
Why Lazy Muscles Don't Get Wasted
14 July 2005 (All day)
Couch potatoes, take heart: Your body may be working overtime to keep you fit. A new study shows that a protein known as Runx1 springs into action to preserve your basic muscle structure even as your muscles shrink from lack of use.
People with sedentary jobs, senior citizens, and others with decreased activity can end up with smaller muscle fibers and reduced nerve supply to their muscles, giving them less strength. For most, this type of atrophy is reversible with exercise. Why muscle structure remains intact during disuse is a puzzle, and the mechanisms that regulate muscle wasting are poorly understood.
Delving into the mystery, Steven Burden, a molecular neurobiologist at New York University Medical School, and colleagues followed a clue--a protein known as Runx1. Runx1 has been found in abundance in atrophying muscle but is nearly absent in healthy muscle. Burden's team examined the effects of atrophy on two groups of inactive mice, one normal and another deprived of Runx1. Muscles shrank in both groups, but the normal mice showed few signs of permanent atrophy. The mice lacking Runx1, however, showed a striking amount of muscle wasting, the team reports 15 July in Genes and Development.
The researchers also examined healthy, active mice, with and without Runx1. Neither group showed signs of muscle wasting. "If everything else is working fine, you don't need Runx1," Burden says. "But if something else goes awry, suddenly it's needed." Exactly how Runx1 prevents muscle wasting remains unclear, but it appears to be multitasking: The researchers identified 29 genes that were affected by the protein, but some were activated and others repressed.
Burden's group has "uncovered an exciting new player," says Alfred Goldberg, a cell biologist at Harvard Medical School in Boston, Massachusetts. But he emphasizes that this study is just one part of the picture. A key question, he says, is whether Runx1 can also prevent muscle atrophy caused by diseases such as diabetes and cancer.