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J Neurogenet. 2018 Mar-Jun;32(2):92-105. doi: 10.1080/01677063.2018.1445247. Epub 2018 May 2.
2
Etiology and functional validation of gastrointestinal motility dysfunction in a zebrafish model of CHARGE syndrome.CHARGE 综合征斑马鱼模型中胃肠道动力功能障碍的病因和功能验证。
FEBS J. 2018 Jun;285(11):2125-2140. doi: 10.1111/febs.14473. Epub 2018 Apr 27.
3
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights.全转录组关联研究精神分裂症和染色质活性,为疾病机制提供了新见解。
Nat Genet. 2018 Apr;50(4):538-548. doi: 10.1038/s41588-018-0092-1. Epub 2018 Apr 9.
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CRISPR/Cas9-induced mutant zebrafish display autism-like behaviors.CRISPR/Cas9 诱导的突变斑马鱼表现出自闭症样行为。
Mol Autism. 2018 Apr 2;9:23. doi: 10.1186/s13229-018-0204-x. eCollection 2018.
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mRNA processing in mutant zebrafish lines generated by chemical and CRISPR-mediated mutagenesis produces unexpected transcripts that escape nonsense-mediated decay.通过化学诱变和CRISPR介导的诱变产生的突变斑马鱼品系中的mRNA加工产生了逃避无义介导衰变的意外转录本。
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10
Zebrafish knockout of Down syndrome gene, , shows social impairments relevant to autism.斑马鱼 Down 综合征基因敲除, 显示与自闭症相关的社交障碍。
Mol Autism. 2017 Sep 29;8:50. doi: 10.1186/s13229-017-0168-2. eCollection 2017.

神经发育障碍的斑马鱼模型:过去、现在与未来

Zebrafish Models of Neurodevelopmental Disorders: Past, Present, and Future.

作者信息

Sakai Catalina, Ijaz Sundas, Hoffman Ellen J

机构信息

Child Study Center, Program on Neurogenetics, Yale School of Medicine, Yale University, New Haven, CT, United States.

Department of Neuroscience, Yale School of Medicine, Yale University, New Haven, CT, United States.

出版信息

Front Mol Neurosci. 2018 Aug 29;11:294. doi: 10.3389/fnmol.2018.00294. eCollection 2018.

DOI:10.3389/fnmol.2018.00294
PMID:30210288
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6123572/
Abstract

Zebrafish are increasingly being utilized as a model system to investigate the function of the growing list of risk genes associated with neurodevelopmental disorders. This is due in large part to the unique features of zebrafish that make them an optimal system for this purpose, including rapid, external development of transparent embryos, which enable the direct visualization of the developing nervous system during early stages, large progenies, which provide considerable tractability for performing high-throughput pharmacological screens to identify small molecule suppressors of simple behavioral phenotypes, and ease of genetic manipulation, which has been greatly facilitated by the advent of CRISPR/Cas9 gene editing technologies. This review article focuses on studies that have harnessed these advantages of the zebrafish system for the functional analysis of genes that are strongly associated with the following neurodevelopmental disorders: autism spectrum disorders (ASD), epilepsy, intellectual disability (ID) and schizophrenia. We focus primarily on studies describing early morphological and behavioral phenotypes during embryonic and larval stages resulting from loss of risk gene function. We highlight insights into basic mechanisms of risk gene function gained from these studies as well as limitations of studies to date. Finally, we discuss advances in neural circuit imaging in zebrafish, which promise to transform research using the zebrafish model by illuminating novel circuit-level mechanisms with relevance to neurodevelopmental disorders.

摘要

斑马鱼正越来越多地被用作一种模型系统,以研究与神经发育障碍相关的越来越多的风险基因的功能。这在很大程度上归因于斑马鱼的独特特征,这些特征使其成为用于此目的的最佳系统,包括透明胚胎的快速、外部发育,这使得在早期阶段能够直接观察发育中的神经系统;大量的后代,这为进行高通量药理学筛选以识别简单行为表型的小分子抑制剂提供了相当大的可操作性;以及易于进行基因操作,CRISPR/Cas9基因编辑技术的出现极大地促进了这一点。这篇综述文章重点关注利用斑马鱼系统的这些优势对与以下神经发育障碍密切相关的基因进行功能分析的研究:自闭症谱系障碍(ASD)、癫痫、智力残疾(ID)和精神分裂症。我们主要关注描述由于风险基因功能丧失而在胚胎和幼体阶段出现的早期形态和行为表型的研究。我们强调从这些研究中获得的对风险基因功能基本机制的见解以及迄今为止研究的局限性。最后,我们讨论斑马鱼神经回路成像的进展,这有望通过阐明与神经发育障碍相关的新的回路水平机制来改变使用斑马鱼模型的研究。