Causal biology of Chd8 haploinsufficiency in complex brain disorders

复杂脑部疾病中 Chd8 单倍体不足的因果生物学

基本信息

批准号：
10621144
负责人：
Alexander Nord
金额：
$ 41.46万
依托单位：
UNIVERSITY OF CALIFORNIA AT DAVIS
依托单位国家：
美国
项目类别：
财政年份：
2019
资助国家：
美国
起止时间：
2019-07-08 至 2025-04-30
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10621144
关键词：
Ablation Acceleration Affect Anatomy Apoptosis Behavior Behavioral Biological Biological Markers Biology Brain Brain Diseases Breeding Caring Cell Cycle Progression Cells Cellular Assay Cerebral cortex ChIP-seq Chromatin Chromatin Remodeling Factor Chromosome Mapping Cognitive Cognitive deficits Complex Cre driver DNA DNA Polymerase II Data Development Diagnosis Dimensions Disease model Electroencephalography Embryo Epigenetic Process Etiology Genes Genetic Risk Genetic Transcription Genetic study Genomics Germ-Line Mutation Glean Goals Heterozygote Hippocampus Human Human Genetics In Vitro Individual Intellectual functioning disability Link Loss of Heterozygosity Macrocephaly Maps Mediating Mental disorders Messenger RNA Modeling Molecular Mus Mutation Neuroanatomy Neurobiology Neurodevelopmental Disorder Neurons Obsessive-Compulsive Disorder Output Pathogenesis Pathologic Pathology Pathway Analysis Pathway interactions Patients Penetrance Phenotype Play Population Proliferating Publishing RNA RNA Polymerase II RNA Processing RNA Splicing RNA metabolism RNA-Protein Interaction Reporting Research Resolution Role Schizophrenia Synapses System Testing Work autism spectrum disorder behavioral phenotyping brain size cell type cohort de novo mutation dosage gene discovery gene network genetic association genome sequencing improved in vitro Model in vivo in vivo imaging interest loss of function loss of function mutation mouse model mutation carrier nerve stem cell neural neurodevelopment neurogenesis neurophysiology novel postnatal postnatal development progenitor risk variant single-cell RNA sequencing stem stem cells synaptogenesis transcriptome

项目摘要

SUMMARY Major gains have been in made in mapping the genetic causes of neurodevelopmental disorders (NDDs). In autism spectrum disorder (ASD) and intellectual disability (ID), de novo mutations to a convergent network of genes encoding chromatin remodeling factors (CRFs) has emerged as one of the strongest components of genetic risk. A major challenge now facing the field is identifying the genomic mechanisms and neurodevelopmental consequences associated with mutations of NDD-associated CRFs. The CRF gene CHD8 has among the highest rates of de novo loss-of-function mutations observed in ASD and ID cohorts with mutations also described in schizophrenia and obsessive compulsive disorder cases, and CHD8 mutation carriers frequently also are diagnosed with macrocephaly. Our work and the work of others have confirmed that Chd8 germline heterozygous mutation in mice causes NDD-relevant pathological changes across genomic, neuroanatomical, and behavioral domains. Network analyses have linked functionality of CHD8 and other NDD-associated CRFs in the developing brain, raising the possibility that understanding CHD8- associated pathological mechanisms during neurodevelopment will reveal generalizable causal pathways mediated by CRF haploinsufficiency. However, independent of a role in early brain development, CHD8, as well as other NDD-associated CRFs, are expressed in neurons and mutation may drive behavioral pathology via neuron-specific impacts in postnatal brain. Thus, resolving developmental versus neuronal causality is essential for understanding CRF-associated mechanisms of NDDs. We will leverage conditional Chd8+/- mice model to dissect in vivo the mechanisms by which Chd8 mutations cause NDD-associated pathology. Our preliminary data suggests that macrocephaly and cognitive deficits are interdependent on pathology during early brain development in Chd8+/- mice, and that the molecular mechanisms are associated with chromatin-associated RNA processing mediated by Chd8. We will apply complementary -omics, cellular assays, and mouse studies to test this model, specifically, we will: 1) establish the mechanisms through which Chd8 haploinsufficiency impacts chromatin and transcription in embryonic brain, 2) characterize cell-type specific impacts of Chd8 haploinsufficiency on neurogenesis during brain development, and 3) define behavioral, EEG, and synaptic pathology caused by Chd8 haploinsufficiency and test whether such pathology is driven via developmental versus neuronal mechanism. This research will map the effect of Chd8 haploinsufficiency in vivo, illuminating mechanisms via which CHD8 dosage-sensitivity contributes to NDD pathology and linking molecular and cellular mechanisms to behavioral and systems level. Importantly, these critical studies cannot be done using in vitro models and such studies of high interest NDD risk genes is necessary to bridge genetic association and mechanistic understanding. By revealing causality for top risk genes such as CHD8, we will establish causal factors and identify novel treatments to improve care of NDDs.

概括在映射神经发育障碍（NDDS）的遗传原因方面已取得了重大收益。在自闭症谱系障碍（ASD）和智力障碍（ID），从头突变与收敛网络编码染色质重塑因子（CRF）的基因已成为最强的组成部分之一遗传风险。现在面临的主要挑战是确定基因组机制和与NDD相关CRF突变有关的神经发育后果。 CRF基因 CHD8具有在ASD和ID队列中观察到的从头丧失功能突变的最高率之一在精神分裂症和强迫症病例和CHD8突变中也描述了突变载体经常也被诊断为脑畸形。我们的工作和其他人的工作已经确认小鼠中CHD8种系杂合突变会导致NDD相关的病理变化基因组，神经解剖和行为领域。网络分析具有CHD8和发育中的大脑中其他NDD相关的CRF，增加了理解CHD8-的可能性神经发育过程中相关的病理机制将揭示可变的因果途径由CRF单倍弥补介导。但是，独立于早期大脑发育中的角色，chd8，以及其他与NDD相关的CRF一样，在神经元中表达，突变可能会驱动行为病理通过神经元特异性的影响在产后大脑中。因此，解决发展与神经元因果关系是了解NDD的CRF相关机制至关重要。我们将利用有条件的CHD8 +/- 小鼠模型在体内剖析CHD8突变引起NDD相关的机制病理。我们的初步数据表明，脑畸形和认知缺陷是相互依存的 CHD8 +/-小鼠早期大脑发育期间的病理，并且分子机制是相关的由CHD8介导的染色质相关RNA处理。我们将应用互补的词，细胞分析和小鼠研究以测试该模型，具体来说，我们将：1）建立通过该模型的机制 CHD8单倍不足会影响胚胎大脑中的染色质和转录，2）表征细胞类型 CHD8单倍体不足对脑发育过程中神经发生的特定影响，3）定义 CHD8单倍不足引起的行为，脑电图和突触病理学，并测试这种病理是否是否通过发育与神经元机制驱动。这项研究将绘制CHD8的效果体内的单倍不足，通过CHD8剂量敏感性有助于NDD的照明机制病理学，将分子和细胞机制与行为和系统水平联系起来。重要的是，这些批判性研究无法使用体外模型进行，因此对NDD风险基因的高兴趣研究是弥合遗传关联和机械理解所必需的。通过揭示最高风险的因果关系诸如CHD8之类的基因，我们将建立因果因素并确定新的治疗方法以改善NDD的护理。