Somatic Mosaicism in Schizophrenia and Control Brains

精神分裂症和控制脑中的体细胞镶嵌

• 批准号: 9305164
• 负责人: Schahram Akbarian
• 金额: $ 148.78万
• 依托单位: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-09-23 至 2020-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9305164
• 关键词: Affect; Autopsy; Biology; Blood; Brain; Cells; ChIP-seq; Code; Communities; Copy Number Polymorphism; DNA; DNA Sequence Alteration; DNA Transposable Elements; DNA sequencing; Data; Data Analyses; Data Analytics; Data Set; Disease; Epigenetic Process; Etiology; Event; FMR1; Family; Fertilization; Follow-Up Studies; Funding; Genes; Genetic; Genetic Transcription; Genome; Genotype; Goals; Human; Human Resources; Individual; Interneurons; Medical; Messenger RNA; Mind; Modification; Molecular; Morbidity - disease rate; Mosaicism; Mutate; Mutation; Neural Pathways; Neurologic; Neurons; Nucleotides; Pathogenesis; Pathology; Pathway Analysis; Pathway interactions; Pattern; Phenotype; Play; Population; Prevalence; Reporting; Research; Research Personnel; Resources; Retrotransposition; Risk; Role; Sampling; Schizophrenia; Somatic Mutation; Synapses; TSC1/2 gene; Testing; Twin Multiple Birth; United States National Institutes of Health; Variant; Work; autism spectrum disorder; brain cell; cell type; cohort; cost; data sharing; design; epigenome; epigenomics; exome; exome sequencing; experimental study; genetic information; genetic risk factor; genome sequencing; genome wide association study; induced pluripotent stem cell; innovative technologies; insight; loss of function; member; mind control; mortality; neuropsychiatry; public health relevance; rare variant; repository; transcriptome sequencing; whole genome

 DESCRIPTION (provided by applicant): Schizophrenia (SCZ) is a generally devastating neuropsychiatric illness with considerable morbidity, mortality, and personal and societal cost. Genetic factors have been strongly implicated via family and twin data, and more recently directly through genome-wide association studies (GWAS) and sequencing studies. Epigenetic modifications play a well-accepted role in a variety of medical and neurological illnesses, and are also implicated in SCZ. Somatic mosaicism is an underexplored, but potentially very important contributor to SCZ. There have been some intriguing hints that somatic mosaicism may play a role in SCZ, but assessment of this possibility awaits rigorous experiments, and that is the overarching goal of this proposal. The primary objective of our project is to identify and characterize the extent of somatic variation in post-mortem human brain samples from individuals with SCZ and controls. Following on work of members of our team, we will rigorously assess the somatic mosaicism in a large cohort of post-mortem human brains from the Common Mind Consortium, which members of our group are already analyzing for genotype, mRNA-seq and epigenome mapping. These brains are from individuals with SCZ (250) and controls (50+). We will look for retrotransposition events, copy number variants (CNVs) and single nucleotide variants (SNVs). All data will be made available to the research community through the Sage Bionetworks Synapse Platform. We have assembled the critical personnel, sample resources, technological know-how, and analytic strategies to be able to assess the role of somatic variation in the brain as well as begin to unravel SCZ biology.

 描述(由申请人提供)：精神分裂症(SCZ)是一种普遍具有破坏性的神经精神疾病，具有相当高的发病率、死亡率以及个人和社会成本。遗传因素通过家族和双胞胎数据被强烈地牵连，最近通过全基因组关联研究和测序研究被直接牵连。表观遗传修饰在各种内科和神经系统疾病中发挥着公认的作用，也与SCZ有关。体细胞嵌合体是SCZ的一个未被研究的潜在的非常重要的贡献者。有一些耐人寻味的迹象表明，体细胞嵌合体可能在SCZ中发挥作用，但对这种可能性的评估有待严格的实验，这也是这项提议的首要目标。我们项目的主要目标是识别和表征死后人类大脑样本中患有SCZ和对照的人的体细胞变异的程度。在我们团队成员工作的基础上，我们将严格评估来自Common Mind Consortium的一大批死后人脑的体细胞嵌合体，我们团队的成员已经在分析基因、mRNA-Seq和表观基因组图谱。这些大脑来自患有SCZ(250人)和对照组(50+)的人。我们将寻找逆转座子事件、拷贝数变异体(CNV)和单核苷酸变异体(SNV)。所有数据将通过Sage Bionetworks Synapse平台提供给研究社区。我们已经汇集了关键人员、样本资源、技术诀窍和分析策略，以便能够评估体细胞变异在大脑中的作用，并开始解开SCZ生物学。