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本文引用的文献

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Cardiovascular findings in duplication 17p11.2 syndrome.17p11.2 综合征的心血管表现。
Genet Med. 2012 Jan;14(1):90-4. doi: 10.1038/gim.0b013e3182329723. Epub 2011 Oct 17.
2
Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.在自闭症中发现的 16p11.2 病变模型中存在剂量依赖性表型。
Proc Natl Acad Sci U S A. 2011 Oct 11;108(41):17076-81. doi: 10.1073/pnas.1114042108. Epub 2011 Oct 3.
3
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.CNTNAP2 的缺失导致癫痫、神经元迁移异常和核心自闭症相关缺陷。
Cell. 2011 Sep 30;147(1):235-46. doi: 10.1016/j.cell.2011.08.040.
4
Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.使用 array CGH 检测自闭症家系基因组中的外显子拷贝数变异,发现 TMLHE 中的一个新缺失。
Hum Mol Genet. 2011 Nov 15;20(22):4360-70. doi: 10.1093/hmg/ddr363. Epub 2011 Aug 24.
5
Preventive and therapeutic types of environmental enrichment counteract beta amyloid pathology by different molecular mechanisms.预防和治疗型环境富集通过不同的分子机制来对抗β淀粉样蛋白病理。
Neurobiol Dis. 2011 Jun;42(3):530-8. doi: 10.1016/j.nbd.2011.03.007. Epub 2011 Mar 22.
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Autism spectrum disorders--a genetics review.自闭症谱系障碍——遗传学综述。
Genet Med. 2011 Apr;13(4):278-94. doi: 10.1097/GIM.0b013e3181ff67ba.
7
Pharmacologic rescue of impaired cognitive flexibility, social deficits, increased aggression, and seizure susceptibility in oxytocin receptor null mice: a neurobehavioral model of autism.神经行为学模型自闭症:神经肽催产素受体缺失小鼠认知灵活性损伤、社会交往缺陷、攻击行为增加和易发性癫痫的药物干预
Biol Psychiatry. 2011 May 1;69(9):875-82. doi: 10.1016/j.biopsych.2010.12.022. Epub 2011 Feb 21.
8
A review of behavioral interventions for the treatment of aggression in individuals with developmental disabilities.发育障碍个体攻击行为的行为干预治疗综述。
Res Dev Disabil. 2011 Mar-Apr;32(2):437-46. doi: 10.1016/j.ridd.2010.12.023. Epub 2011 Jan 15.
9
Enriched environment effects on behavior, memory and BDNF in low and high exploratory mice.丰富环境对低探索性和高探索性小鼠行为、记忆和 BDNF 的影响。
Physiol Behav. 2011 Mar 28;102(5):475-80. doi: 10.1016/j.physbeh.2010.12.025. Epub 2011 Jan 13.
10
Aggression in low functioning children and adolescents with autistic disorder.自闭症谱系障碍低功能儿童和青少年的攻击行为。
PLoS One. 2010 Dec 21;5(12):e14358. doi: 10.1371/journal.pone.0014358.

富养改善了基于脉络膜新生血管的自闭症样特征的动物模型的行为反应。

Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits.

机构信息

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Hum Mol Genet. 2012 Jul 15;21(14):3083-96. doi: 10.1093/hmg/dds124. Epub 2012 Apr 5.

DOI:10.1093/hmg/dds124
PMID:22492990
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3384379/
Abstract

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.

摘要

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。