A new, fast and inexpensive way to mutate genes and large, non-gene pieces of DNA has been developed by University of Utah geneticists. They tested the method by mutating a gene involved in bone formation, resulting in short, malformed tail and limbs in the mutant mouse on the left, compared with the skeleton of a normal mouse on the right. The new method promises to speed efforts to learn more about how non-gene portions of DNA control genes to cause human defects and diseases. Credit: Sen Wu, University of Utah Genes account for only 2.5 percent of DNA in the human genetic blueprint, yet diseases can result not only from mutant genes, but from mutations of other DNA that controls genes. University of Utah researchers report in the journal Nature Genetics that they have developed a faster, less expensive technique for mutating those large, non-gene stretches of DNA.

A gene responsible for the single most common cause of hearing loss among white adults, otosclerosis, has been identified for the first time, a scientist told the annual conference of the European Society of Human Genetics in Nice, France. Ms Melissa Thys, from the Department of Medical Genetics, University of Antwerp, Belgium, said that this finding may be a step towards new treatments for otosclerosis, which affects approximately 1 in 250 people.

Many people are drinking too much water, including sports drinks, when exercising, a practice that could put some individuals engaging in prolonged types of endurance exercise at risk of potentially lethal water intoxication, say international experts who study disorders of water metabolism. Such exercise includes marathons, triathlons, and long distance cycling.

Celebrated in Buddhist temples and cultivated for its wood and cottony fibers, the kapok tree now is upsetting an idea that biologists have clung to for decades: the notion that African and South American rainforests are similar because the continents were connected 96 million years ago.

A comparison of three parasite species that cause Leishmaniasis has identified a small number of genes, many new to biology, that will provide a framework to target the search for new treatments. Leishmaniasis is a devastating disease that affects about two million people each year and threatens one-fifth of the world's population and new treatments are desperately needed.