Genetic Mutation For Quadrupedality Gets Closer

The discovery of four families in which some members only walk on all fours (quadrupedality) may help us understand how humans, unlike other primates, are able to walk for long periods on only two legs, according to professor Tayfun Ozcelik, of Bilkent University, Ankara, Turkey, who presented his study at the annual conference of the European Society of Human Genetics tomorrow. The quadrupedal families in Turkey previously attracted attention in 2005, when they were discovered. Now the Turkish team reports that they have found the first gene implicated in quadrupedal locomotion in these families. Ozcelik and colleagues, studied four unrelated families where some members were affected by the rare quadrupedic condition, Unertan syndrome, which is also associated with imperfect articulation of speech, mental retardation, and defects in the cerebellum, a part of the brain involved in motor control. They found that the affected individuals in two families had mutations in the gene responsible for the expression of very low density lipoprotein receptor (VLDLR), a protein which is known to be critical to the proper functioning of the cerebellum during development. read more

Read the whole article on Scientific Blogging

More from Scientific Blogging

Related