基因突变与自闭症

Scientists have known that abnormal brain growth is associated with autism spectrum¹ disorder². However, the relationship between the two has not been well understood. Now, scientists from the Florida campus of The Scripps Research Institute (TSRI) have shown that mutations in a specific gene³ that is disrupted in some individuals with autism results in too much growth throughout the brain, and yet surprisingly specific problems in social interactions, at least in mouse models that mimic⁴ this risk factor in humans. "What was striking is that these were basically normal animals in terms of behavior, but there were consistent deficits⁵ in tests of social interaction and recognition -- which approximate a major symptom of autism," said Damon Page, a TSRI biologist who led the study. "This suggests that when most parts of the brain are overgrown, the brain somehow adapts to it with minimal⁶ effects on behavior in general. However, brain circuits relevant to social behavior are more vulnerable or less able to tolerate this overgrowth."   The study, which focuses on the gene phosphatase（磷酸酶） and tensin homolog (PTEN), was recently published online ahead of print by the journal Human Molecular⁷ Genetics.   Autism spectrum disorder is a neurodevelopmental disorder involving a range of symptoms and disabilities involving social deficits and communication difficulties, repetitive behaviors and interests, and sometimes cognitive⁸ delays. The disorder affects in approximately one percent of the population; some 80 percent of those diagnosed are male.   In a previous study, Page and colleagues found that mutations in Pten causes increased brain size and social deficits, with both symptoms being exacerbated⁹ by a second "hit" to a gene that regulates levels of the neurotransmitter serotonin（血清素） in the brain. In the new study, the TSRI team set out to explore whether mutations in Pten result in widespread or localized overgrowth within the brain, and whether changes in brain growth are associated with broad or selective deficits in tests of autism-relevant behaviors in genetically¹⁰ altered mice. The team tested mice for autism spectrum disorder-related behaviors including mood, anxiety, intellectual, and circadian rhythm and/or sleep abnormalities.   The researchers found that Pten mutant mice showed altered social behavior, but few other changes -- a more subtle change than would have been predicted given broad expression and critical cellular¹¹ function of the gene.   Intriguingly#p#分页标题#e#¹², some of the more subtle impairments were sex-specific. In addition to social impairments, males with the mutated gene showed abnormalities related to repetitive behavior and mood/anxiety, while females exhibited additional circadian activity and emotional learning problems.   The results raise the question of how mutations in PTEN, a general regulator of growth, can have relatively¹³ selective effects on behavior and cognitive development. One idea is that PTEN mutations may desynchronize the normal pattern of growth in key cell types -- the study points to dopamine neurons -- that are relevant for social behavior.   "Timing¹⁴ is everything," Page said. "Connections have to form in the right place at the right time for circuits to develop normally. Circuitry involved in social behavior may turn out to be particularly vulnerable to the effects of poorly coordinated¹⁵ growth."