Scientists link evolved, mutated gene module to syndromic autism
By Debra Kain, Scott LaFee
27 January 2012
A team led by researchers at the University of California, San Diego School of Medicine reports that newly discovered mutations in an evolved assembly of genes cause Joubert syndrome, a form of syndromic autism
|Image using an electron microscope shows a cilium growing from a neuron. -Gleeson lab, UC San Diego|
The findings are published in the January 26 online issue of Science Express.
Joubert syndrome is a rare, recessive brain condition characterised by malformation or underdevelopment of the cerebellum and brainstem. The disease is due specifically to alterations in cellular primary cilia – antenna-like structures found on most cells.
The consequence is a range of distinct physical and cognitive disabilities, including poor muscle control, and mental retardation. Up to 40 per cent of Joubert syndrome patients meet clinical criteria for autism, as well as other neurocognitive disorders, so it is considered a syndromic form of autism.
The cause or causes of Joubert syndrome are not well-understood. Researchers looked at mutations in the TMEM216 gene, which had previously been linked to the syndrome. However, only half of the expected Joubert syndrome patients exhibit TMEM216 gene mutations; the other half did not. Using genomic sequencing, the research team, led by Joseph G. Gleeson, MD, professor of neurosciences and pediatrics at UC San Diego, broadened their inquiry and discovered a second culprit: mutations in a neighboring gene called TMEM138.
''It is extraordinarily rare for two adjacent genes to cause the same human disease,'' said Gleeson. ''The mystery that emerged from this was whether these two adjacent, non-duplicated genes causing indistinguishable disease have functional connections at the gene or protein level.''