First language gene identified. Researchers find mutation linked to speech disordergreenspun.com : LUSENET : Poole's Roost II : One Thread |
http://www.msnbc.com/news/637430.asp
First language gene identified Researchers find mutation linked to speech disorder
MSNBC NEWS SERVICES
Oct. 3 — British scientists say they’ve discovered the first gene tied to a language and speech disorder, raising hopes that the genetics revolution is closer to identifying the biological roots of conscious thought and, perhaps, refining what it means to be human. Fisher, Monaco and Faraneh Vargha-Khadem of the Institute of Child Health in London led a team of scientists that pinpointed the gene by studying three generations of a large family in England with a history of speech problems, identified only as the KEs. ‘It is extraordinary to think that we have now got an entry point into the understanding of one of the most important features that distinguish us from other animals.’
— ANTHONY MONACO
Wellcome Trust Centre for Human Genetics in OxfordCALLED FOXP2, the gene produces a protein that turns other genes on and off. Scientists believe it could hold the key to why people suffer from speech problems.
It is not specifically a gene that enables us to talk. Instead, researchers say they discovered a mutated form of the gene, which is responsible for a protein that enables the brain’s language circuitry to function.
“We have identified a way of getting at the pathways and neural networks involved in speech and language from a genetics point of view,” said study co-author Simon Fisher, a geneticist at the Wellcome Trust Centre for Human Genetics in Oxford.
Because FOXP2 works with other genes and proteins, Fisher and his colleagues believe its identification could help unlock the molecular mysteries of speech.
“It is extraordinary to think that we have now got an entry point into the understanding of one of the most important features that distinguish us from other animals,” said Anthony Monaco, also of Wellcome Trust Centre.
FINDING JUST THE BEGINNING
But even the researchers who located the gene say their discovery is just the beginning and caution it would be wrong to heap too many expectations onto the damaged version of a single gene.
About half of its 24 members are affected with a speech disorder that impairs movement of the mouth, lips and tongue and also creates problems with phonemes and grammar, such as using proper word tense.
Using information from the Human Genome Project, the scientists found differences in the sequence of DNA letters in FOXP2, located on chromosome 7, in some members of the family. The research is reported in the latest edition of the science journal Nature. Researchers believe the mutation on FOXP2 is causing a breakdown in the gene’s ability to regulate other genes, resulting in the disorder.
“This gene controls other genes, and we need to find out which ones it’s controlling,” Monaco said. “We can then think about better therapies and diagnostic issues.”
Once the mutation was identified, it was consistent in the KE family, lending weight to the researchers’ conclusions, said Steven Pinker, of the Department of Brain and Cognitive Sciences at the Massachusetts Institute of Technology, author of an accompanying commentary on the research.
“When identifying a gene with a behavioral disorder it’s unusual to find a contingency so perfect,” Pinker said. “Everyone with the mutated version of the gene has the disorder and those without the mutated gene do not.”
Genome of plague germ decoded
GENETIC BASIS FOR LANGUAGE?
Other researchers said it’s also premature to link this study to the debate over whether a gene or genes are solely responsible for language in humans.