Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Hum Mol Genet. 2012 Jul 15;21(14):3083-96. doi: 10.1093/hmg/dds124. Epub 2012 Apr 5.
Potocki-Lupski syndrome (PTLS; MIM #610883), characterized by neurobehavioral abnormalities, intellectual disability and congenital anomalies, is caused by a 3.7-Mb duplication in 17p11.2. Neurobehavioral studies determined that ∼70-90% of PTLS subjects tested positive for autism or autism spectrum disorder (ASD). We previously chromosomally engineered a mouse model for PTLS (Dp(11)17/+) with a duplication of a 2-Mb genomic interval syntenic to the PTLS region and identified consistent behavioral abnormalities in this mouse model. We now report extensive phenotyping with behavioral assays established to evaluate core and associated autistic-like traits, including tests for social abnormalities, ultrasonic vocalizations, perseverative and stereotypic behaviors, anxiety, learning and memory deficits and motor defects. Alterations were identified in both core and associated ASD-like traits. Rearing this animal model in an enriched environment mitigated some, and even rescued selected, neurobehavioral abnormalities, suggesting a role for gene-environment interactions in the determination of copy number variation-mediated autism severity.
波托茨基-卢普斯基综合征(PTLS;MIM #610883)的特征是神经行为异常、智力残疾和先天性异常,由 17p11.2 处的 3.7Mb 重复引起。神经行为研究确定,接受测试的 PTLS 受试者中有∼70-90% 为自闭症或自闭症谱系障碍(ASD)阳性。我们之前通过染色体工程构建了一种具有与 PTLS 区域同源的 2Mb 基因组间隔重复的 PTLS 小鼠模型,并在该小鼠模型中鉴定出一致的行为异常。我们现在报告了广泛的表型,包括用于评估核心和相关类自闭症特征的行为测定,包括社交异常、超声发声、持续和刻板行为、焦虑、学习和记忆缺陷以及运动缺陷的测试。在核心和相关的 ASD 样特征中都发现了改变。在丰富环境中饲养这种动物模型减轻了一些,甚至挽救了一些特定的神经行为异常,这表明基因-环境相互作用在决定拷贝数变异介导的自闭症严重程度方面发挥了作用。