for decades, autism（自闭症） researchers have faced a baffling 1: how to 2 a 3 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 4 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 6 and proteins go 7 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 8 pick 20 people with autism, the cause of each person's disease will be unique," said principal 9 dr. daniel geschwind, the gordon and virginia macdonald 10 chair in human genetics and a professor of neurology and 11 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 12 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 13 linked to autism, the group zeroed in on the 14 cortex（大脑皮层） , the most evolved part of the human brain.
the researchers focused on 5 expression — how a gene's 15 sequence is copied into rna, which directs the synthesis of 16 17 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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