For decades, autism（自闭症） researchers have faced a baffling riddle1: how to unravel2 a disorder3 that leaves no known physical trace as it develops in the brain. Now a UCLA study is the first to reveal how the disorder makes its mark at the molecular4 level, resulting in an autistic brain that differs dramatically in structure from a healthy one. Published May 25 in the advance online edition of Nature, the findings provide new insight into how genes6 and proteins go awry7 in autism to alter the mind.
The discovery also identifies a new line of attack for researchers, who currently face a vast array of potential fronts for tackling the neurological disease and identifying its diverse causes.
"If you randomly8 pick 20 people with autism, the cause of each person's disease will be unique," said principal investigator9 Dr. Daniel Geschwind, the Gordon and Virginia MacDonald Distinguished10 Chair in Human Genetics and a professor of neurology and psychiatry11 at the David Geffen School of Medicine at UCLA. "Yet when we examined how genes and proteins interact in autistic people's brains, we saw well-defined shared patterns. This common thread could hold the key to pinpointing12 the disorder's origins."
The research team, led by Geschwind, included scientists from the University of Toronto and King's College London. They compared brain tissue samples obtained after death from 19 autism patients and 17 healthy volunteers. After profiling three brain areas previously13 linked to autism, the group zeroed in on the cerebral14 cortex（大脑皮层） , the most evolved part of the human brain.
The researchers focused on gene5 expression — how a gene's DNA15 sequence is copied into RNA, which directs the synthesis of cellular16 molecules17 called proteins. Each protein is assigned a specific task by the gene to perform in the cell.
By measuring gene-expression levels in the cerebral cortex, the team uncovered consistent differences in how genes in autistic and healthy brains encode information.
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