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自闭症组织计划死后脑组织的基因型资源。

A genotype resource for postmortem brain samples from the Autism Tissue Program.

机构信息

Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Autism Res. 2011 Apr;4(2):89-97. doi: 10.1002/aur.173. Epub 2011 Jan 19.

DOI:10.1002/aur.173
PMID:21254448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4605268/
Abstract

The Autism Tissue Program (ATP), a science program of Autism Speaks, provides researchers with access to well-characterized postmortem brain tissues. Researchers access these tissues through a peer-reviewed, project-based approval process, and obtain related clinical information from a secure, online informatics portal. However, few of these samples have DNA banked from other sources (such as a blood sample from the same individual), hindering genotype-phenotype correlation and interpretation of gene expression data derived from the banked brain tissue. Here, we describe an initiative to extract DNA from Brodmann Area 19, and genotype these samples using both the Affymetrix Genome-Wide Human SNP Array 6.0 and the Illumina Human1M-Duo DNA Analysis BeadChip genome-wide microarray technologies. We additionally verify reported gender, and infer ethnic background from the single nucleotide polymorphism data. We have also used a rigorous, multiple algorithm approach to identify genomic copy number variation (CNV) from these array data. Following an initial proof of principle study using two samples, 52 experimental samples, consisting of 27 subjects with confirmed or suspected autism and related disorders, 5 subjects with cytogenetically visible duplications of 15q, 2 with epilepsy and 18 age-matched normal controls were processed, yielding high-quality genotype data in all cases. The genotype and CNV data are provided via the ATP informatics portal as a resource for the autism research community.

摘要

自闭症组织计划(ATP)是自闭症之声的一个科学项目,为研究人员提供了获取经过良好特征描述的死后脑组织的机会。研究人员通过经过同行评审的基于项目的批准程序来获取这些组织,并从安全的在线信息学门户获得相关的临床信息。然而,这些样本中很少有从其他来源(如同一人的血液样本)保存的 DNA,这阻碍了基因型 - 表型相关性以及对来自保存的脑组织的基因表达数据的解释。在这里,我们描述了一项从布罗德曼区域 19 提取 DNA 并使用 Affymetrix Genome-Wide Human SNP Array 6.0 和 Illumina Human1M-Duo DNA Analysis BeadChip 全基因组微阵列技术对这些样本进行基因分型的计划。我们还通过单核苷酸多态性数据验证了报告的性别,并推断了种族背景。我们还使用了严格的、多算法方法,从这些阵列数据中识别基因组拷贝数变异(CNV)。在使用两个样本进行初步原理验证研究之后,处理了 52 个实验样本,其中包括 27 名确诊或疑似自闭症及相关障碍的受试者、5 名具有 15q 可见性倍增的受试者、2 名患有癫痫的受试者和 18 名年龄匹配的正常对照者,所有情况下都产生了高质量的基因分型数据。基因型和 CNV 数据通过 ATP 信息学门户提供,作为自闭症研究社区的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93eb/4605268/bc6ff07024b8/nihms726748f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93eb/4605268/bc6ff07024b8/nihms726748f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93eb/4605268/bc6ff07024b8/nihms726748f1.jpg

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2
Functional impact of global rare copy number variation in autism spectrum disorders.自闭症谱系障碍中全球罕见拷贝数变异的功能影响。
Nature. 2010 Jul 15;466(7304):368-72. doi: 10.1038/nature09146. Epub 2010 Jun 9.
3
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.NRXN1(神经连接素-1)缺失易导致广泛的发育障碍。
自闭症谱系障碍脑组织的突变景观。
Genes (Basel). 2022 Jan 24;13(2):207. doi: 10.3390/genes13020207.
4
Somatic Mosaicism and Autism Spectrum Disorder.体细胞嵌合体与自闭症谱系障碍。
Genes (Basel). 2021 Oct 26;12(11):1699. doi: 10.3390/genes12111699.
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Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome.父源 20 号染色体全部单亲二体导致的 Beckwith-Wiedemann 综合征患儿
Genes (Basel). 2021 Jan 27;12(2):172. doi: 10.3390/genes12020172.
6
Proteomic Investigations of Autism Brain Identify Known and Novel Pathogenetic Processes.蛋白质组学研究自闭症大脑识别已知和新的发病机制过程。
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8
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